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2449 Cards in this Set
- Front
- Back
What kind of protein is dynein?
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Dynein is an ATPase.
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What is the protein responsible for unwinding the DNA double helix?
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DNA Helicases
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Describe the role of dynein in cilia structure.
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Dynein links peripheral 9 doublets of microtubules.
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What are Nissl bodies?
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rough ER
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What is the primary source of energy for the Liver?
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Amino acids, lipids, glucose, fructose, and lactate
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Define poikilocytosis
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varying cell shapes
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Which cells are rich in smooth ER?
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1. liver hepatocytes, 2. steroid hormone-producing cells of adrenal cortex.
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How does dynein function in cilia function?
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Dynein causes the bending of cilium by differential sliding of doublets.
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Describe the histological structure of sinusoids of the liver.
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Irregular 'capillaries' with round pores 100-200 nm in diameter and no basement membrane.
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What are the functions of the lymph node?
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1. Nonspecific filtration by macrophages. 2. storage/proliferation of B and T cells 3. Ab production.
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What is the function of Nissl bodies?
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Synthesize enzymes (e.g. ChAT) and peptide neurotransmitters.
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Name a protein involved in the structure of hemidesmosomes.
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Integrin.
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Define anisocytosis
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varying cell sizes
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For the following genetic transfer procedure, explain the process: Transduction
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Phage-mediated cell to cell DNA transfer
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For the following genetic transfer procedure, explain the process: Transformation
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Purified DNA taken up by a cell
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For the following genetic transfer procedure, explain the process: Transposition
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DNA transfer to same or another chromosome or plasmid WITHIN a cell
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For the following genetic transfer procedure, give the types of cells involved: Transformation
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Prokaryotic or eukaryotic
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For the following genetic transfer procedure, give the types of cells involved: Transposition
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Prokaryotic or eukaryotic
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For the following genetic transfer procedure, give the nature of DNA transferred: Transduction
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Generalized transduction: Any gene Specialized transduction: Only certain genes
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For the following genetic transfer procedure, give the nature of DNA transferred: Transposition
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DNA sequences ""jumping genes""
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Woman with anxiety about an exam is told to relax and imagine going through the steps. What process is this?
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Systematic desensitization.
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Girl can groom herself, can hop on 1 foot, and has an imaginary friend. How old is she?
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4 years old.
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Person demands only the best and most famous doctor in town. What is the personality disorder?
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Narcissism.
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Observational Study. Sample chosen on presence of absence of disease. Information collected about exposure.
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Case-control Study.
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Observational study. sample chosen based on presence of absence of risk factors. Subjects followed over time for disease.
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Cohort Study.
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List 4 ways to reduce bias in a study.
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1. Blind studies. 2. Placebo responses. 3. Case-crossover design. 4. Randomization
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(a/b)/(c/d)
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OR - approximates RR if prevalence of disease is not too high.
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[a/(a+b)]/[c/(c+d)]
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RR - relative risk
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Attributable risk formula?
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[a/(a+b)]-[c/(c+d)]
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Reduced precision means
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increase in random error
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Reduced accuracy means
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increase in systematic error
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Number needed to treat
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NNT = 1/(Ic-Ie); The number of pts that need to be treated to prevent 1 additional bad outcome.
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Validity is ...
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whether the test truly measures what it purports to measure. A test is valid if it measures what it is supposed to measure.
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A positive skew distribution ...
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is asymmetry with the tail to the right, hump on the left (mean>median>mode)
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a Negative skew distribution ...
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is asymmetry with the tail to the left, hump on the right (mean<median<mode)
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Power
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the probability of rejecting the null hypothesis when it is in fact false.
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Power in a study depends on what two things ...
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1. total number of endpoints experienced by the population; 2. difference in compliance between treatment groups
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Confidence interval
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mean +/- 1.96 (SEM) If the CI includes 0, H0 is accepted.
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Normal (Gaussian) distribution has what percentage of the population in each standard deviation?
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68% within 1 SD, 95% within 2 SDs, 99.7% within 3 SDs.
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Correlation coefficient indicates
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the strength of the correlation between two variables. The sign indicates a positive or negative.
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What is Primary Disease Prevention?
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Prevent the disease from occuring.
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What is Secondary Disease Prevention?
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Early detection of the disease.
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What is Tertiary Disease prevention?
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Reduce mobidity from the disease.
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What are important preventative measure for patients with DM?
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Eye exams, foot exams, urine tests.
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What are important preventive measures for pts with drug abuse problems?
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HIV test, TB test, Hep immunizations.
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What are important preventive measures for pts with alcoholism?
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influenza, pneumococcal immunizations and TB testing
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What is an important preventive measure to offer obese pts?
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Blood sugar testing for diabetes.
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What is an important preventive measure to offer homeless pts or recent immigrants?
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TB tests
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What tests are important for pts engaging in high risk sexual behavior?
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HIV, Hep B, Syphilis, gonorrhea, chlamydia tests.
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What are the leading causes of death for infants in the US?
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1. Congenital anomalies 2. Short gestation/LBW 3. SIDS 4. Maternal complications of pregnancy 5. RDS
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What are the leading causes of death for children age 1-14 in the US?
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1. Injuries 2. Cancer 3. Congenital anomalies 4. Homicide 5. Heart disease
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What are the leading causes of death for people 15-24 years of age in the US?
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1. Injuries 2. Homicide 3. Suicide 4. Cancer 5. Heart disease
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What are the leading causes of death for adults 25-64 yo in the US?
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1. Cancer 2. Heart disease 3. Injuries 4. Suicide 5. Stroke
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What are the leading causes of death for adults over the age of 65 in the US?
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1. Heart disease 2. Cancer 3. Stroke 4. COPD 5. Pneumonia 6. Influenza
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Define Transference.
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When the patient projects feelings stemming from their personal life onto their physician.
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Define Countertransference.
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When the doctor projects feelings stemming from their personal life onto the pt.
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What is the IQ cutoff for diagnosis of mental retardation?
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IQ < 70 or 2 SD below mean.
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True or False: IQ tests are objective test.
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True ... but they are NOT projective tests.
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Are IQ scores correlated with genetic factors or school achievement?
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Yes to both ... but more highly correlated to school achievement.
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In what circumstances can a physician break confidentiality?
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1. potential harm to others is serious. 2. likelihood of harm to self is great. 3. no alternative means exist to warn and protect those at risk
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What steps may a physician take to prevent harm caused by a patients infectious disease?
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Physician may have a duty to warn public health officials (reportable diseases) and identify people at risk.
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What is the Tarasoff decision?
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A law requiring physician to directly inform and protect a potential victim from harm; may involve a breach of confidentiality.
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May a physician break confidentiality if in cases of an automobile accident?
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Only if they suspect that the driver was impaired
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How may a physician handle a suicidal or homicidal patient?
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The physician may hold the patient involuntarily for a period of time ... or until psychiatric evaluation is completed.
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A civil suit under negligence requires what 3 things?
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1. Physician breach of duty to patient (Dereliction) 2. patient suffers harm (damage) 3. Breach of duty causes harm (Direct)
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What is the most common factor leading to litigation between the physician and pt?
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poor communication.
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In a criminal suit the burden of proof is "beyond a reasonable doubt" ... in a malpractice suit the burden of proof is ...
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more likely than not
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Define Anosognia
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unaware that one is ill
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Define Autotopagnosia
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unable to locate ones own body parts
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Define depersonalization
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body seems unreal or dissociated
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What is involved in orienting the patient
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person, place, and time
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What is the order of orientation loss in a disoriented patient?
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time goes first, then place, and last person
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What is Korsakoff's anmesia
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classic anterograde anmesia caused by a thymine deficiency.
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A alcoholic patient presents with anterograde amnesia, and confabulations. What is the likely diagnosis?
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Korsakoffs amnesia
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How many signs of maladaptive substance abuse must be present in a years time to diagnose substance dependance?
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3 or more.
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What are Freud's three structures of the mind?
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Id, Ego, Superego
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The Topographic theory of the mind deals with what three topography?
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Conscious, precocious, and unconscious
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What are some negative symptoms of schizophrenia?
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flat affect, social withdrawal, thought blocking, lack of motivation
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How long must a patient experience symptoms of schizophrenia for a diagnosis?
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Periods of psychosis or disturbed behavior lasting > 6 months.
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What are the 5 types of schizophrenia?
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1. Disorganized 2. Catatonic 3. paranoid 4. Undifferentiated 5. Residual
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What are the 4 A's of schizophrenia described by Bleuler?
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1. Ambivalence 2. Autism 3. Affect (blunted) 4. Associations (loose)
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What is schizoaffective disorder?
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a combination of schizophrenia and a mood disorder.
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What is the lifetime prevalence of schizophrenia?
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1.5% (males=females, blacks=whites)
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Describe a pt with a Cluster A personality disorder.
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odd or eccentric, cannot develop meaningful social relationships.
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What are 3 types of Cluster A personality disorders?
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1. Paranoid 2. Schizoid 3. Schizotypal
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What is a Paranoid personality disorder?
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distrust and suspiciousness, projection is main defense mechanism
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What is a Schizoid personality disorder?
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voluntary social withdrawal, limited emotional expression
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What is a Schizotypal personality disorder
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interpersonal awkwardness, odd thought patterns and appearance
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Personality disorders that lead pts to be erratic, emotional, or dramatic and have a genetic association with mood disorders
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Cluster B
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What are the 4 types of Cluster B personality disorders
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1. Antisocial 2. Borderline 3. Histrionic 4. Narcissistic
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Describe an antisocial personality disorder.
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disregard for and violation of rights of others, crimilatiy, males more often affected than females.
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Describe a borderline personality disorder
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unstable mood and behavior, impulsiveness, sense of emptiness. women more often affected than men.
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Describe a Histrionic personality disorder.
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excessive emotionality, somatization, attention seeking, sexually provacative.
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Describe a Narcissistic personality disorder.
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grandiosity, sense of entitlement, may demand ""top"" physician, or best health care
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Pts with personality disorders that leave them anxious or fearful and have a genetic association with anxiety disorders
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Cluster C personality disorders
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List 3 types of Cluster C personality disorders
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1. Avoidant 2. Obsessive-Compulsive 3. Dependent
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Describe an avoidant personality disorder.
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sensitive to rejection, socially inhibited, timid, feelings of inadequacy
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Describe OCD
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preoccupation with order, perfectionism, and control
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Describe a dependent personality disorder.
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submissive and clinging, excessive need to be taken care of, low self confidence
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A child puts everything in their mouth. How old are they?
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1st year of life.
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An infant sits with support, how old is she?
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4 months
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An infant stands with help, how old is he?
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8 months
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A baby is crawling, how old is she?
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9 months
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A little girl just learned to walk on her own, how old is she?
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13 months
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A child has just learned to climb the stairs alone, how old is he?
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18 months
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At what age does an emergence of hand preference first appear?
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18 months
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A child has lots of energy, can walk backwards, turn doorknobs, unscrew jars, and scribble with crayons. How old is she?
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2 years
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A child can descend the stairs normally and hop on one foot. How old is she?
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4 years
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At what age will a child develop complete sphincter control (toilet trained)?
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5 years
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At 5 years of age, what percentage of the adult brain mass does the child have?
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75.00%
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A child has most of her permanent teeth, how old is he?
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11 years
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A child plays patty cake and peek a boo, how old is she?
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10 months
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A baby is experiencing stranger anxiety, how old is he?
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6 months
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A baby has started showing signs of normal separation anxiety, how old is she?
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1 year.
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The parent is the central figure and issues of trust are key, how old is the child?
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1st year of life.
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A toddler will engage in parallel play, but ""no"" is still her favorite word, how old is she?
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1 year
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A toddler is selfish and self centered, aggressive, and tends to imitate mannerisms and activities, how old is he?
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2 years
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A baby can follow objects to midline, how old is she?
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4 months
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A baby is putting his feet in his mouth, how old is he?
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5 months
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A baby will approach a toy with one hand, and then change hands with the toy, how old is she?
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1st year of life
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A baby first laughs out loud, how old is she?
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4 months
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A baby has started saying ""ma-ma-ma"" and ""da-da-da"", how old is he?
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10 months
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In Piaget's Cognitive Development, at what age does a baby achieve object permanence?
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1 year
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A baby kicks and throws a ball, how old is he?
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1 year
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A toddler is using two word sentences and has a vocabulary of about 250 words, how old is he?
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1 year
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A toddler has started using pronouns and shows great variations in timing of language. How old is she?
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2 years
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A toddler is using complete sentences and has a vocabulary of 900 words, although he appears to understand 4x as many.
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3 years
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A child tells stories, uses prepositions, plurals, and has discovered compound sentences, how old is she?
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4 years
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A child can stand on her tiptoes, how old is she?
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30 months
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A child who can use symbols and has concrete use of objects and use of symbols along with a strong egocentrism?
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2 years
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At what age is gender identity fixed?
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3 years
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A child knows her full name and what sex she is, how old is she?
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3 years
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Two children are observed to be taking turns with a toy, how old are they?
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3 years
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At what age is a child likely to start grooming themselves and brushing their own teeth?
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4 years
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A child can point to and count three objects, repeat four digits, and name colors correctly, how old is she?
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4 years
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A child has an imaginary friend and this is entirely normal for this age group, how old is she?
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4 years
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Two children are caught "playing doctor", at what age does this curiosity manifest?
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4 years
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A child is having terrible nightmares and needs the light left on at night for fear of monsters, how old is he?
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4 years
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At what age does a child adopt personal speech patterns?
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adolescence (12+)
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At what age does communication become the focus of friendships?
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adolescence (12+)
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A child repeatedly asks for the meaning of words, how old is she?
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5 years
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A child can count 10 objects correctly, how old is she?
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5 years
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At what age will a child first express romantic feelings towards others, perhaps as an Oedipal phase?
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5 years
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A child can draw a recognizable man, dress and undress herself, and catch a ball with two hands, how old is she?
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5 years
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A child can ride a bicycle, print letters, and her father is excited because she is gaining athletic skill and coordination.
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6-12 years
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By age 12, about how many words will a child have in their vocabulary?
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About 50,000
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A child shows a shift from egocentric to social speech and incomplete sentences decline, how old is he?
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6-12 years
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Identity is the critical issue in what age range?
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adolescence (12+)
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Conformity is most important for what age range?
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11-12 years
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When do cross gender relationships first take off?
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adolescence (12+)
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A teacher has noticed many of her kids are quitting organized sports, how old is her class likely to be?
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adolescents (12+)
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A teacher has noticed that for her kids, the ""rules of the game"" are paramount. How old is her class?
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6-12 years
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At what age range are organized sports first possible?
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6-12 years
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Demonstrating competence is key for what age group?
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6-12 years
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At this age there is a separation of the sexes and sexual feelings are not apparent.
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6-12 years
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At this age there is an adherence to logic, concrete operations, and no hypotheticals.
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6-12 years
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Children of this age group can use seriation, and have a personal sense of right and wrong.
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6-12 years
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Children can handle hypotheticals, being systematic problem solving and deal with the past, present, and future. Age?
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adolescence (12+)
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APGAR stands for what?
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Appearance (color); Pulse; Grimace; Activity; Respiration
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How do you calculate an APGAR score?
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Score 0-2 at 1 and 5 inutes in each of 5 categories.
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What the three levels of appearance (color) on the APGAR scale?
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0 = blue/pale 1=trunk pink 2=all pink
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What describes the three levels of pulse on the APGAR score?
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0= 0 1= <100 2= >100
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What describes the three levels of reflex irritability (grimace) on the APGAR scale?
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0= none 1= grimace 2 = grimace + cough
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Describe the 3 levels of muscle tone on the apgar scale.
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0 = limp 1 = some 2 = active
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Describe the three levels of respiratory effort on the APGAR scale.
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0 = none 1= irregular 2 = regular
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What is the definition of low birth weight in grams?
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< 2500 g
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List some complications of low birth weight.
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infections; respiratory distress syndrome; necrotizing enterocolitis; intraventricular hemorrhage; persistent fetal circulation
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What are two likely etiologies for low birth weight?
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prematurity and intrauterine growth retardation
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Long term infant deprivation of affection results in the 4 W's ...
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Weak, Wordless, Wanting, Wary
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How long does deprivation of affection need to continue before changes may be irreversible?
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> 6 months
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List some effects of long term deprivation of affection in infants.
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1. Decreased muscle tone 2. Poor language skills 3. Poor socialization skills 4. Lack of basic trust 5. Anaclitic depression 6. Weight loss 7. Physical illness
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What is anaclitic depression?
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Depression in an infant owing to continued separation from caregiver - it can result in failure to thrive.
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An infant becomes withdrawn and unresponsive when left in a crowded daycare for a few weeks, what is the problem?
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Anaclitic depression
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What stimuli may cause children to regress to younger behavior?
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Stress: physical illness, birth of a new sibling, tiredness.
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How many children die each year in the United States from physical abuse?
|
about 3000.
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At what age are most children sexually abused?
|
9-12 years.
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Describe autistic disorder
|
pts have severe communication problems and difficulty forming relationships. repetative behavior, savants, and below normal intelligence.
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Describe Asperger syndrome
|
Milder form of autism involving problems with social relationships and repetative behavior. Children are of normal intelligence and lack social deficits.
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Describe Rett disorder
|
X-linked disorder seen only in girls. Characterized by loss of development and mental retardation appearing at about 4 years.
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Describe ADHD
|
limited attention span and hyperactivity. children are emotionally labile, impulsive, and prone to accidents. Normal intelligence
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Why aren't boys seen with Rett syndrome?
|
With this X-linked disorder, boys die in utero.
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What is the treatment for ADHD?
|
methylphenidate (Ritalin)
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Describe conduct disorder
|
continued behavior violating social norms.
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Describe oppositional definant disorder.
|
A form of conduct disorder when the child is noncompliant in the absence of criminality.
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Describe Tourette's syndrome.
|
motor/vocal tics and involuntary profanity. Onsent < 18 years.
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What is the treatment for Tourette's?
|
haloperidol
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Describe separation anxiety disorder.
|
fear of loss of attachment figure leading to factitious physical complaints to avoid going to school. Common in children ages 7-8.
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What are hallucinations?
|
perceptions in the absence of external stimuli.
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What are Illusions?
|
misinterpretations of actual external stimuli.
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What are Delusions?
|
false beliefs not shared with other members of culture/subculture that are firmly maintained despite obvious proof to the contrary.
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Describe the difference between a delusion and a loose association.
|
A delusion is a disorder in the content of thought (the actual idea), while a loose association is a disorder in the form of the thought
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Patients with psychomotor epilepsy will commonly experience what kind of hallucination?
|
olfactory hallucination.
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Patients with DTs or cocaine abusers may experience what kind of hallucinations?
|
tactile hallucinations
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What is a hypnagogic hallucination?
|
A hallucination that occurs when going to sleep.
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What is a hypnopompic hallucination?
|
A hallucination that occurs when waking from sleep.
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|
How many heroin addicts are there in the United States?
|
About 500,000
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|
A diagnosis of hepatitis, abscesses, overdose, hemorrhoids, AIDS, or right sided endocarditis. Consider?
|
heroin addiction.
|
|
What is Delirium tremens?
|
Life threatening alcohol withdrawal syndrome that peaks 2-5 days after the last drink.
|
|
tachycardia, tremors, and anxiety followed by hallucinations, delusions, and confusion in an alcoholic may be signs of?
|
delirium tremens.
|
|
List risk factors for suicide completion
|
SAD PERSONS"": Sex (male), Age, Depression, Previous attempt, Ethanol, RAtional thought, Sickness, Organized plan, No spouse, Social support lacking.
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|
What is a personality disorder?
|
When personality traits become inflexible and maladaptive, causing impariment in social or occupational functioning or subjective distress
|
|
What does the phrase ""Mature women wear a SASH"" indicate
|
Mature ego defenses: Sublimation, Altruism, Supression, and Humor
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What are ego defenses?
|
automatic and UNCONCIOUS reactions to psychological stress.
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|
aggressive impulses used to succeed in sports is an example of what ego defense?
|
sublimation.
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What is sublimation as an ego defense?
|
process whereby one replaces an unacceptable wish with a course of action that is similar to the wish but does not conflict with one's value system.
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|
A patient with libidinous thoughts enters a monastery This is an example of what ego defense?
|
Reaction formation.
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An 8 year old child under stress begins bed wetting again. This is an example of what ego defense?
|
Regression.
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What is the basic underlying mechanism for all ego defenses?
|
repression.
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What is dysthymia?
|
A milder form of depression lasting at least 2 years.
|
|
Describe a major depressive episode.
|
at least 5 for 2 weeks. sleep changes, loss of interest, guilt, less energy, less concentration, change in appetite, psychomotor retardation, suicidal, depressed. SIG E CAPS
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A major depressive episode MUST include one of two symptoms, these are ...
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1. depressed mood, or 2. anhedonia
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A patients has experienced 2 major depressive episodes with a symptom free interval of 2 months, what is the diagnosis?
|
Recurrent Major Depressive Disorder.
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|
What is the lifetime prevalence of major depressive disorder in women? in men?
|
10-25% in women and 5-12% in men.
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|
What is the key to diagnosing dementia?
|
Ruling out delirium.
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|
In an elderly person who seems to apparently have dementia, what other condition should be considered?
|
Depression.
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Describe the difference between dementia and delirium.
|
Delirium= changes in sensorium while Dementia = changes in memory. Dementia is commonly irreversible.
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|
What is the most common psychiatric illness on medical and surgical floors?
|
Delirium.
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If a patient on a hospital ward presents with delirium, what drugs should you check for in their med list?
|
Drugs with anticholinergic effects.
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|
Pt presents with dec attention span and dec level of arousal, disorganized thinking, hallucinations, illusions
|
Delirium
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What is the key to diagnosis of delirium?
|
Waxing and waning level of conciousness, develops rapidly.
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|
A man who has lost his wife appears to be in shock, and expresses denial, guilt and somatic symptoms for the 4 months.
|
Normal bereavement.
|
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How long does normal bereavement last?
|
Typically 6 months to a year.
|
|
When does grief become pathologic?
|
When it becomes excessively intense or prolonged, delayed, inhibited, or denied.
|
|
What are the functions of the frontal lobe?
|
concentration; orientation; language; abstraction; judgement; motor regulation; mood
|
|
What deficit is most notable in frontal lobe lesions?
|
lack of social judgement.
|
|
how often does REM sleep occur while sleeping?
|
every 90 minutes. Duration of REM sleep increases throughout the night.
|
|
What is the principal neurotransmitter involved in REM sleep?
|
ACh.
|
|
What are the neurotransmitter changes associated with anxiety?
|
increase in NE decrease in GABA and 5HT
|
|
What neurotransmitter changes are associated with Alzheimer's dementia?
|
decreases ACh
|
|
What neurotransmitter changes are associated with Huntington's Disease?
|
decrease GABA and ACh
|
|
Name the 4 reflexes that are present at birth.
|
1. Mono 2. Rooting 3. Palmar 4. Babinski
|
|
What is the Mono reflex?
|
extension of limbs when startled
|
|
What is the rooting reflex?
|
nipple seeking
|
|
What are the Kubler-Ross dying stages?
|
1. Denial 2. Anger 3. Bargaining 4. Grieving 5. Acceptance
|
|
Describe "substance abuse"
|
Maladaptive pattern leading to clinically significant impairment or distress - 1 or more symptom must be present for 1 year
|
|
What are the symptoms of substance abuse?
|
1. recurrent use = failure to fulfill major obligation 2. recurrent use in physically hazardous situation 3. recurrent use related legal problems
|
|
What is substance dependence?
|
Maladaptive pattern of substance use defined as 3 or more of the defining symptoms for at least a year.
|
|
What are the symptoms of substance dependence?
|
Tolerance, Withdrawal, Taken in larger amounts, Desire to cut down, Lots of energy spent obtaining substance, Activities reduced, Use despite problems
|
|
Describe adjustment disorder.
|
emotional symptoms causing impairment following an identifiable psychosocial stressor lasting < 6 months.
|
|
Describe generalized anxiety disorder.
|
uncontrollable anxiety unrelated to a specific person, situation, or event. May include GI symptoms, fatigue, and difficulty concentrating.
|
|
Describe post traumatic stress disorder.
|
intense fear, helplessness, or horror, in which a person who experienced or witnessed an event that involved actual or threatened death or injury
|
|
What is the difference between acute stress and PTSD?
|
acute stress lasts 2-4 weeks, PTSD lasts > 1 month and causes distress or social/occupational impairment.
|
|
What is Gamophobia?
|
fear of marriage.
|
|
What is algophobia?
|
fear of pain.
|
|
what is acrophobia?
|
fear of heights.
|
|
What is agoraphobia?
|
fear of open places.
|
|
What is a specific phobia?
|
fear that is excessive or unreasonable, cued by presence or anticipation of a specific object or entity.
|
|
In reference to a somatoform disorder, describe a primary gain.
|
Primary gain = what symptom does for patients internal psyche.
|
|
In reference to a somatoform disorder, describe a secondary gain.
|
Secondary gain = what symptom gets for patient (ie sympathy)
|
|
In reference to a somatoform disorder, describe a tertiary gain.
|
Tertiary gain = what the caretaker gets (MD on an interesting case)
|
|
What does "PANIC" indicate.
|
The symptoms of a panic attack: palpiations, abdominal distress, nausea, increased perspiration, chest pain, chills, choking.
|
|
What is panic disorder?
|
discrete period of intense fear and discomfort, peaking in 10 minutes, including 4 symptoms, and must be diagnosed in the context of the occurence.
|
|
Describe changes in sleep patterns with advanced age.
|
decrease REM sleep, slow wave sleep; increase sleep latency, wakings during the night.
|
|
What are the most common medical conditions due to advanced age?
|
arthritis, HTN, CVD.
|
|
What percent of time is spent in stage 1 sleep?
|
5.00%
|
|
What percent of time is spent in stage 2 sleep?
|
45.00%
|
|
What percent of time is spent in stage 3-4 sleep?
|
25.00%
|
|
What percent of time is spent in REM sleep?
|
25.00%
|
|
When do you experience an alpha waveform?
|
awake, but drowsy with eyes closed.
|
|
In light sleep, what waveform predominates?
|
theta
|
|
in deeper sleep, stage 2, what waveform predominates?
|
Sleep spindles and K complexes.
|
|
In stage 3-4 sleep, the deepest non REM sleep, what waveforms predominate?
|
delta waves (lowest frequency, highest amplitude)
|
|
When will a person sleepwalk, have night terrors, or wet the bed?
|
In delta sleep (stage 3-4)
|
|
when does dreaming occur?
|
in REM sleep
|
|
What does "At night, BATS drinK Blood" indicate
|
waveforms of sleepstages: Beta, Alpha, Theta, Spindles and K forms, Delta, Beta.
|
|
What is the key to initiating sleep?
|
5HT predominance of raphe nucleus
|
|
What neurotransmitter reduces REM sleep?
|
NE
|
|
What are EOM movements during REM sleep due to?
|
activity of the PPRF (paramedian pontine reticular formation / conjugate gaze center)
|
|
Why are benzodiazepines good for night terrors and sleep walking?
|
They shorten stage 4 sleep.
|
|
What drug shortens stage 4 sleep and is used to treat enuresis?
|
Imipramine.
|
|
What is a conversion disorder?
|
A somatoform disorder where symptoms suggest motor or sensory neurologic or physical disorder - but tests and physical examination are negative.
|
|
What is somatoform pain disorder?
|
prolonged pain that is not explained completely by illness.
|
|
What is hypochondriasis?
|
misinterpretation of normal physical findings, leading to preoccupation with fear of having a serious illness in spite of medical reassurance.
|
|
what is somatization disorder?
|
variety of complaints in multiple organ systems.
|
|
what is body dysmorphic disorder?
|
patient convinced that part of their own anatomy is malformed.
|
|
what is pseudocyesis?
|
a false belief of being pregnant associated with objective physical signs of pregnancy.
|
|
What are the major adverse effects of ECT?
|
disorientation, and amnesia.
|
|
When is ECT used?
|
For major depressive disorder refractory to all other treatment.
|
|
What is a hypomanic episode?
|
like a manic episode, except the mood disturbance is not as severe. it does not require hospitalization and there are no psychotic features.
|
|
What is malingering?
|
patient consciously fakes or claims to have a disorder in order to attain a specific gain.
|
|
What is factitious disorder?
|
a patient consciously creates symptoms in order to assume the ""sick"" roll to get medical attention.
|
|
What is Munchausen's syndrome?
|
manifests as a chronic history of multiple hosptital admissions and willingness to receive invasive procedures.
|
|
What is Munchausen's syndrome by proxy?
|
when the illness in a child is caused by a parent. the motivation is unconcious.
|
|
Describe bipolar disorder.
|
6 separate criteria sets exist for bipolar disorders with combinations of manic, hypomanic, and depressed episodes.
|
|
What is cyclothymic disorder
|
a milder form of bipolar disorder lasting at least 2 years.
|
|
What is a manic episode?
|
distinct period of abnormally and persistently elevated, expansive, or irritable mood lasting at least one week.
|
|
During a manic episode, 3 or more symptoms are present ... list the 7 symptoms.
|
1. distractability 2. insomnia 3. grandiosity 4. flight of ideas 5. increase in activity/agitation 6. pressured speech 7. thoughtlessness (DIG FAST)
|
|
Disinhibition, emotional lability, slurred speech, ataxia, coma, and blackouts are indicative of what substance?
|
alcohol.
|
|
what symptoms may a patient withdrawing from alcohol experience?
|
tremor, tachycardia, HTN, malaise, nausea, seizures, DTs, tremulousness, agitation, hallucinations.
|
|
When a patient stops smoking cigarettes, what symptoms might they expect during withdrawal?
|
irritability, headache, anxiety, weight gain, and cravings.
|
|
a patient who consumes lots of coffee might experience what symptoms?
|
restlessness, insomnia, increased diruesis, muscle twitching, cardiac arrhythmias
|
|
When a patient stops caffeine consumption, what symptoms might they expect?
|
headache, lethargy, depression, weight gain.
|
|
A patient presents to the ER with nausea and vomiting, constipation, and pinpoint pupils. What substance?
|
opiods.
|
|
When a patient ODs on opiods, what symptom are you most concerned with?
|
seizures ... may be life threatening.
|
|
a pt presents with amnesia, ataxia, somnolence, and minor respiratory distress. No alcohol. what substance?
|
Benzodiazepines.
|
|
Are benzos addictive?
|
if consumed with alcohol.
|
|
When a patient stops taking benzos, what symptoms may they experience?
|
rebound anxiety, seizures, tremor, and insomnia
|
|
a patient presents to the ER with major respiratory depression, their friends state they "took something"
|
barbiturates
|
|
In addition to anxiety, seizures, and delirium, You are concerned about in a patient who is withdrawing from barbiturates?
|
life threatening cardiovascular collapse.
|
|
a patient presents with euphoria, anxiety, paranoid delusions, impaired judgement, and the munchies ?
|
marijuana.
|
|
Are there withdrawal symptoms from marijuana?
|
social withdrawal.
|
|
a patient presents with marked anxiety, delusions, visual hallucinations, flashbacks, and pupil dilation.
|
LSD.
|
|
a pt presents with agitation, pupillary dilation, tachycardia, euphoria, fever, hallucinations and awake for 36 hr
|
amphetamines.
|
|
what symptoms can a patient withdrawing from amphetamines expect?
|
post crash depression, lethargy, headache, stomach cramps, hunger, hypersomnolence.
|
|
a pt presents euphoric with psychomotor agitation, tachycardia, pupillary dilation, hallucinations, and angina..
|
cocain.
|
|
what fatal effect of cocain are you worried about?
|
sudden cardiac death.
|
|
what can a patient in withdrawal from cocain expect to experience?
|
post crash depression and suicidality, hypersomnolence, fatigue, malaise, and severe psychological craving.
|
|
a pt presents with fever and psychomotor agitation, belligerent and impulsive, and has horizontal and vertical nystagmus.
|
PCP.
|
|
When a patient is withdrawing from PCP, what symptoms are you concerned about?
|
sudden onset of severe, random, homicidal thought
|
|
A patient recovering from a PCP intoxication appears to be having a recurrence of intoxication symptoms... why?
|
reabsorption of PCP from the GI tract.
|
|
What is the BMI numerical cutoff for an obesity?
|
> 30.0
|
|
A patient complains of sexual dysfunction, what 3 things are on your differential?
|
1. drugs 2. disease 3. psychological
|
|
What diseases may lead to sexual dysfunction?
|
depression or DM
|
|
What drugs can lead to sexual dysfunction?
|
anti-HTN, neuroleptics, SSRI, EtOH.
|
|
Describe the physiological effects of stress.
|
Stress induces production of FFA, 17-OH corticosteroids, and catecholamines. it affects water absorption, muscular tonicity, and gastrocolic reflex
|
|
A patient with depression will typically show these three changes in their sleep stages:
|
1. decrease slow wave sleep 2. decrease REM latency 3. early morning awakening
|
|
What is the most important screening question for depression?
|
Are you experiencing early morning awakening?
|
|
Describe narcolepsy.
|
person falls asleep suddenly. May include hypnagogic or hypnopompic hallucinations.
|
|
A person with narcolepsy starts off their sleep cycle with what sleep stage?
|
REM
|
|
What is cataplexy?
|
sudden collapse while awake. may be present in some patients with narcolepsy.
|
|
What is the treatment for narcolepsy?
|
amphetamines.
|
|
What is the treatment for sleep apnea?
|
weight loss, CPAP, surgery
|
|
What symptoms and signs is sleep apnea associated with:
|
obesity, loud snoring, systemic or pulmonary HTN, arrhythmias, and possibly sudden death.
|
|
What toxin inhibits lipoic acid?
|
Arsenic
|
|
What are the net reactants and products in the reaction that Pyruvate Dehydrogenase catalyzes?
|
Reactants:1. Pyruvate 2. CoA 3. NAD Products:1. Acetyl CoA 2. CO2 3. NADH
|
|
Pyruvate dehydrogenase deficiency: Congenital or Acquired
|
Both. Acquired cases happen in cases of B1 deficiency (such as in alcoholics.)
|
|
What is the rate-limiting step of the TCA?
|
Isocitrate to alpha-ketoglutarate by isocitrate dehydrogenase
|
|
Which tissues and organs primarily convert pyruvate into lactate?
|
1. RBCs and WBCs 2. Lens and cornea 3. Renal medulla 4. Testes
|
|
What stimulates and inhibits isocitrate dehydrogenase?
|
Stimulate: ADP; Inhibit: 1. ATP 2. NADH
|
|
Which reagent sequentially removes C-terminal residues from a polypeptide?
|
Carboxypeptidase
|
|
What activated carriers carry: 1-carbon units
|
1. Tetrahydrofolates (originally as formyl then methyl) 2. Biotin (as CO2) 3. S-adenosyl-methionine (as CH3)
|
|
What is the mechanism of oligomycin?
|
ATPase inhibition
|
|
Cathode: What does it attract?
|
Cations
|
|
What kind of inheritance and mutation is the alpha-1-antitrypsin deficiency?
|
Autosomal recessive, single purine substitution (GAG to AAG)
|
|
What is this molecule an activated carrier of?: S-adenosyl-methionine
|
Methyl groups
|
|
What is the mechanism of electron transport inhibitors?
|
1. Directly inhibit electron transport causing: 2. Decreased protein gradient and decrease in O2 consumption, thereby: 3. Blocking ATP synthesis
|
|
What stimulates and inhibits alpha-ketoglutarate dehydrogenase?
|
Stimulate: Nothing; Inhibit: 1. ATP 2. NADH 3. Succinyl CoA
|
|
Pyruvate dehydrogenase: What inhibits it?
|
NADH (You produce NADH, soon there'll be more of me.), Acetyl-CoA (Enough of me, save your pyrvuate.)
|
|
Where does the Cori Cycle happen?
|
In the liver and muscle/RBCs Liver: Pyruvate converts to glucose Muscle/RBCs: Glucose converts to Pyruvate
|
|
What is rotenone?
|
An electron transport inhibitor.
|
|
What enzymes and cofactors are used in conversion of pyruvate to alanine?
|
Enzyme: Alanine Transaminase (ALT) Cofactors: None
|
|
Where in the electron transport chain is O2 reduced to 2H2O?
|
Complex IV
|
|
Pyruvate dehydrogenase deficiency: Treatment
|
Increased intake of ketogenic nutrients (such as high fat content or increased lysine and leucine)
|
|
What stimulates and inhibits citrate synthase?
|
Stimulate: Nothing; Inhibit: ATP
|
|
What is the enzyme involved in processing tRNA
|
Aminoacyl tRNA synthetase (uses 1 ATP)
|
|
What is antimycin A?
|
An electron transport inhibitor.
|
|
Name three classes of oxidative phosphorylation poisons.
|
1. Electron transport inhibitors 2. ATPase inhibitors 3. Uncoupling agents
|
|
What enzymes and cofactors are used in conversion of pyruvate to oxaloacetate?
|
Enzyme: Pyruvate Carboxylase (contains biotin and magnesium) Cofactors: CO2 and ATP
|
|
# of Aas in one turn of alpha-helix?
|
3.6
|
|
What disease state is glycolytic enzyme deficiency generally associated with?
|
Hemolytic anemia
|
|
What stimulates pyruvate dehydrogenase?
|
ADP (need more ATP. Inhibits PD kinase and stimulates PD phosphatase.)
|
|
Energy malnutrition leads to what disease?
|
Marasmus (as opposed to Kwashiorkor from protein malnutrition)
|
|
Which major metabolic reactions require Thiamine as a cofactor?
|
TCA: Pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase, HMP shunt: Transketolase
|
|
Role of ATP in protein synthesis
|
ATP does tRNA Activation (charging)
|
|
Where is fructokinase found?
|
Liver (processes most dietary fructose), kidney, small intestine
|
|
Amino acids that disrupt alpha-helix?
|
proline, many charged aas, bulky side chains
|
|
Where in glycolysis and TCA does CO2 come off?
|
3 places: Pyruvate to Acetyl CoA, Isocitrate to alpha-ketoglutarate, and alpha-ketoglutarate to Succinyl CoA
|
|
Enzyme function: DNA helicase
|
Separates the two strands of DNA into single strands allowing for replication to occur.
|
|
What enzyme converts Galactose-1-Phosphate to Glucose-1-Phosphate?
|
Uridyl transferase
|
|
What is the clinical presentation of fructose intolerance?
|
hypoglycemia, jaundice, cirrhosis, and vomiting
|
|
What is the etiology of classic galactosemia?
|
1. Absence of galactose-1-phosphate uridyl transferase 2. Build up of toxic substances including galactitol
|
|
I-Cell disease: Pathophysiology
|
Inability of cell to phosphorylate mannose residues on glycoproteins indicating that they are lysosome bound.
|
|
Sources of Succinyl CoA?
|
TCA intermediate, and from odd chained fatty acids, and from propionyl coA from metabolism of branched-chain amino acids.
|
|
What is the clinical presentation of essential fructosuria?
|
Fructose appears in the blood and urine
|
|
What does sorbitol dehydrogenase do?
|
Oxidizes sorbitol to fructose.
|
|
Which post-translational modification involves hydroxylation?
|
post-translational covalent alteration
|
|
Hunter's Syndrome vs Hurler's Syndrome: Mental retardation?
|
Both (Hunter's ranges from mild to severe)
|
|
An acid with a pKa of x serves as a buffer best at x + what?
|
positive or negative 1 (equal amounts of charged and uncharged acid)
|
|
Which tissues have cotransport of glucose?
|
Epithelial cells of the intestine, renal tubular cells, and choroid plexus
|
|
Heparin: Where found?/Distinguishing characteristic from other GAGs
|
Intracellular compound (unlike other GAGs). Found in mast cells of artery walls, especially in lungs, liver, and skin
|
|
Which reagent sequentially removes N-terminal residues from a polypeptide?
|
Phenylisothiocyanate (Edman degradation)
|
|
Where do GLUT1 receptors predominate over other GLUT receptors?
|
RBCs
|
|
Name the enzymes used in the oxygen-dependent respiratory burst.
|
1. NADPH oxidase 2. Superoxide dismutase 3. Myeloperoxidase 4. Catalase/Glutathione peroxidase 5. Glutathione reductase 6. G-6-P D
|
|
Where is pyruvate carboxylase found and not found?
|
Found in mitochondria of liver and kidney cells, not foudn in mitochondria of muscle
|
|
What does aldose reductase do?
|
Reduces glucose to sorbitol
|
|
Where is the mutation for G6PD?
|
Point mutation in coding region of the G6PD gene (X-linked)
|
|
What is the famed respiratory burst?
|
The rapid conversion of O2 to superoxide using NADPH.
|
|
Where is aldose reductase found?
|
Lens, retina, Schwann cells, kidney, placenta, RBCs, and gonads
|
|
Chondroitin Sulfate: Use/Mechanism
|
Form proteoglycan aggregates. Cartilage: Bind collagen and hold fibers in a tight, strong network
|
|
Pepsin cleaves peptides at which side of what residues?
|
C-terminal side of tyrosine, phenylalanine, and tryptophan (all have phenyl groups, these are the same bonds as chymotrypsin.
|
|
What is a glycoside?
|
Carbohydrate attached to non-carbohydrate structures.
|
|
Hyaluronic Acid: Use/Mechanism
|
Lubricant and shock absorber
|
|
What are the key enzymes of the pentose phosphate shunt and are the reactions reversible or irreversible?
|
1. Glucose-6-phosphate dehydrogenase (irreversible) 2. Transketolase (reversible)
|
|
How does glucagon stimulate gluconeogenesis?
|
Regulation of F2,6-BP and inactivation of Pyruvate Kinase via elevation of cAMP-dependent protein kinase A.
|
|
Hunter's Syndrome vs Hurler's Syndrome: Enzyme deficiency
|
Hunter's: Iduronate sulfatase, Hurler's: alpha-L-iduronidase
|
|
Trypsin cleaves peptides at which side of what residues?
|
C-terminal of lysine or arginine (the most basic amino acids)
|
|
What is the mechanism of 2,4-dinitrophenol?
|
Uncoupling agent
|
|
What enzyme phosphorylates glucose with high affinity?
|
Hexokinase
|
|
What is NADPH used for?
|
1. Reductive biosynthesis 2. Reduction of oxygen directly and hydrogen peroxide indirectly 3. Cytochrome P-450 mono-oxygenase system
|
|
How does galactokinase deficiency present?
|
1. Galactosemia 2. Galactosuria More severe symptoms such as cataracts, hepatosplenomegaly and mental retardation can follow.
|
|
Phosphofructokinase-1: What does it do?
|
PFK-1 1-phosphorylates fructose-6-phosphate to produce Fructose-1,6-Bisphosphate.
|
|
Heparan Sulfate: Where found?/Distinguishing characteristic from other GAGs
|
Extracellular, unlike heparin. Found in basement membrane and as a ubiquitous component of cell surfaces.
|
|
Glucokinase: Where is it found and why does it do what it does?
|
Found in the liver and pancreatic beta cells. Phosphorylates glucose to sequester it after a big meal.
|
|
What are the two most common glycolytic enzyme deficiencies?
|
Pyruvate kinase (95% of cases) followed by glucose phosphate isomerase (4% of cases)
|
|
Dermatan Sulfate: Where found?
|
Found in skin, blood vessels, and heart valves
|
|
In nucleic acids, what kind of substitution is a transversion?
|
TransVersion = conVersion between types (Purine for pyrimidine or vice versa)
|
|
What does alpha-amanitin do?
|
Inhibits RNA polymerase II leading to hepatic necrosis
|
|
Name the irreversible enzymes in glycolysis.
|
1. Hexokinase 2. Phosphofructokinase-1 3. Pyruvate kinase 4. Pyruvate dehydrogenase
|
|
In aerobic metabolism of glucose, which pathway produces 38 ATP?
|
Malate shuttle
|
|
What activated carriers carry: CH3 groups
|
1. S-adenosyl-methionine 2. N5-methyl-THF
|
|
What is the presentation of arsenic toxicity?
|
1. Vomiting 2. Rice water stools 3. Garlic breath
|
|
This oxidation accounts for about 2/3 of the total oxygen consumption and ATP production in most animals
|
Oxidation of acetyl coA to CO2 and H2O.
|
|
What activated carriers carry: Formyl groups
|
N10-formyl-THF
|
|
Where in the electron transport chain is ADP converted to ATP?
|
Complex V aka ATP synthase aka mitochondrial ATPase
|
|
What histologic change is seen in G6PD deficiency
|
Heinz bodies within red blood cells
|
|
Which amino acids are necessary for purine synthesis?
|
Glycine, Aspartate, Glutamine
|
|
Which is active?: Phosphorylated or dephosphorylated pyruvate dehydrogenase
|
Dephosphorylated.
|
|
Uses of Succinyl CoA?
|
TCA intermediate, and biosynthesis of heme
|
|
How much ATP is produced by anaerobic glycolysis?
|
2 ATP per glucose
|
|
Which amino acids are basic?
|
Arginine, Lysine and Histidine Arginine and Lysine are increased in histones which bind negatively charged DNA. Histidine has no charge at body pH.
|
|
Where in the TCA does FADH2 come from?
|
Succinate to fumarate.
|
|
Pyruvate kinase: What inhibits it?
|
ATP (don't need more of me), Alanine (I came from pyruvate, so we don't need any more.)
|
|
Inhibitors of electron transport from Cytochrome a+a3 to Oxygen?
|
Cyanide, CO, and Sodium azide
|
|
What does 4-epimerase do?
|
converts between UDP-galactose and UDP-glucose
|
|
Where in the TCA does NADH come from?
|
Pyruvate to Acetyl CoA, Isocitrate to alpha-ketoglutarate, alpha-ketoglutarate to succinyl coA, Malate to Oxaloacetate
|
|
How much ATP is produced by the citric acid cycle per molecule of glucose?
|
24 ATP
|
|
What is a reducing sugar?
|
A monosaccharide where the anomeric carbon (Carbon 1) is free.
|
|
What is the relation of polyols to sugars?
|
Polyols are monosaccharides where the carbonyl group is reduced to an alcohol.
|
|
What are the properties of the genetic code?
|
Unambiguous, Degenerate/ redundant, Commaless/nonoverlapping, and Universal
|
|
Which tissues (7) need glucose as fuel?
|
Brain, RBCs, Renal medulla, lens, cornea, testes, exercising muscle
|
|
What does the mRNA initiation codon code for?
|
Methionine in eukaryotes. formyl-methionine in prokaryotes.
|
|
What happens during post-translational covalent alterations?
|
Either: 1. Phosphorylation 2. Glycosylation 3. Hydroxylation
|
|
What is the etiology of fructose intolerance?
|
1. Lack of aldolase B 2. Build up of Fructose-1-Phosphate 3. Decrease in available phosphate 4. Inhibition of glycogenolysis and gluconeogenesis
|
|
What activates isocitrate dehydrogenase?
|
ADP
|
|
Which post-translational modification involves phosphorylation?
|
post-translational covalent alteration
|
|
Where in the cell does the following occur: Fatty acid synthesis
|
Cytoplasm
|
|
What is the difference in presentation between von Gierke's disease and fructose intolerance?
|
Both have hypoglycemia, jaundice, cirrhosis and vomiting. von Gierke's disease also has lactic acidosis whereas fructose intolerance does not.
|
|
Role of P site in protein synthesis
|
P site accomodates growing Peptide.
|
|
Where is Fructose 1-6 bisphosphatase found?
|
Liver and kidney
|
|
How many ATP molecules are produced by aerobic metabolism of glucose?
|
38 via the Malate shuttle, and 36 via the G3P shuttle.
|
|
What is this molecule an activated carrier of?: Thiamine Pyrophosphate
|
Aldehydes
|
|
Pyruvate dehydrogenase deficiency: Mechanism
|
Backup of pyruvate and alanine leads to lactic acidosis.
|
|
Hunter's Syndrome vs Hurler's Syndrome: Physical deformity?
|
Hunter's: Mild to severe, Hurler's: Dwarfing, coarse facial features, (gargoylism)
|
|
What is the mechanism of ATPase inhibitors?
|
1. Directly inhibit mitochondrial ATPase causing: 2. Increased protein gradient and increased oxygen consumption, but no ATP is production
|
|
What are the 5 cofactors necessary for pyrvuate dehydrogenase and alpha-ketoglutarate dehydrogenase?
|
Lipoic acid plus the first four B vitamins in their active forms: 1. B1: TPP 2. B2: FAD 3. B3: NAD 4. B5: CoA
|
|
What activated carriers carry: Aldehydes
|
Thiamine Pyrophosphate
|
|
In aerobic metabolism of glucose, which pathway produces 36 ATP?
|
G3P shuttle
|
|
What is the mechanism of CN?
|
Electron transport inhibition
|
|
Inhibitors of electron transport from FMNH2 to Coenzyme Q?
|
Amytal and Rotenone
|
|
Ubiquitin or Ubiquinone: Coenzyme Q in oxidative phosphorylation
|
Ubiquinone
|
|
Eukaryotic genome: Trigger for replication
|
Consensus sequence of AT-rich base pairs
|
|
What characterizes a promoter of gene expression?
|
AT-rich upstream sequence with TATA and CAAT boxes
|
|
Amino acid binding to tRNA: Where (on the tRNA) and how?
|
Where: 3' end How: Covalently
|
|
Special points about RNA polymerase II
|
1. Opens DNA at promoter site 2. Inhibited by alpha-amanitin
|
|
What activates pyruvate dehydrogenase?
|
1. Increased NAD/NADH ratio; 2. Increased ADP;3. Ca2+;
|
|
What activated carriers carry: Electrons
|
1. NADH 2. NADPH 3. FADH2
|
|
What are the consequences of the altered NADH/NAD ratio seen in alcoholics?
|
Short-term: Hypoglycemia, Long-term: Hepatic fatty change
|
|
What is this molecule an activated carrier of?: Tetrahydrofolate
|
1-carbon units
|
|
What are the net reactants in glycolysis?
|
Glucose, 2 Phosphates, 2 ADP, 2 NAD
|
|
What activated carriers carry: Phosphoryl
|
ATP and GTP
|
|
What is this molecule an activated carrier of?: Biotin
|
CO2
|
|
What are exceptions to universality of genetic code?
|
Mitochondria, Archaebacteria, Mycoplasma, and Some Yeasts
|
|
What is on the 3' end of a nucleotide
|
Hydroxyl group
|
|
Types of DNA repair
|
Single stranded: Nucleotide excision repair, Base excision repair, and Mismatch repair; Double Stranded: Nonhomologous end joining
|
|
DNA polymerase I: Which direction does it proofread?
|
5' to 3'
|
|
DNA polymerase III: Which direction does it proofread?
|
3' to 5'
|
|
Enzyme function: DNA polymerase III
|
Elongates the chain
|
|
What enzyme is missing in hereditary fructose intolerance?
|
Aldolase B
|
|
What enzyme converts UDP-glucose to UDP-galactose?
|
Uridyl transferase
|
|
When is genetic code not commaless/nonoverlapping?
|
In some viruses
|
|
Which amino acids are acidic?
|
Aspartate and glutamate are negatively charged at body pH
|
|
Where is sorbitol dehydrogenase found?
|
Liver and gonads (ovaries, seminal vesicles, sperm)
|
|
How does lactose intolerance present?
|
1. Bloating 2. Cramps 3. Osmotic diarrhea
|
|
Hunter's Syndrome vs Hurler's Syndrome: Inheritance?
|
Hunter's: X-linked Recessive, Hurler's (and all other mucopolysaccharidoses): Autosomal recessive
|
|
How many nucleotides does tRNA contain?
|
75 to 90 nucleotides
|
|
Pyruvate kinase: What stimulates it?
|
Fructose-1,6-BP (I was told we needed more ATP, so here I am, so you better move the line along.)
|
|
What enzyme converts galactose to galactitol?
|
Aldose reductase
|
|
When is NADPH used?
|
1. Anabolic process (steroid and fatty acid synthesis) 2. Respiratory burst 3. P-450
|
|
Zinc deficiency: Presentation
|
Delayed wound healing, hypogonadism, and decreased adult hair (axillary, facial, pubic)
|
|
What does aldose reductase do?
|
Converts galactose to galactitol
|
|
Zinc deficiency: Predisposes to what?
|
Alcoholic cirrhosis
|
|
What inhibits isocitrate dehydrogenase?
|
ATP and NADH
|
|
What is the mechanism behind chronic fatty change in alcoholics?
|
1. Ethanol metabolism leads to an increased NADH/NAD ratio in the liver. 2. This ratio prefers fatty acid synthesis over glycolysis.
|
|
I-Cell disease: Presentation
|
Skeletal abnormalities, restricted joint movement, coarse facial features, severe psychomotor impairment, death by 8 years
|
|
What is this molecule an activated carrier of?: Lipoamide
|
Acyl
|
|
What reaction does citrate synthase catalyze?
|
Oxaloacetate and acetyl coA combine to yield citrate.
|
|
mRNA initiation codons
|
1. AUG (inAUGurates protein synthesis) 2. GUG (rarely)
|
|
What does Uridyl transferase do?
|
1. converts UDP-glucose to UDP-galactose 2. converts Galactose-1-Phosphate to Glucose-1-Phosphate
|
|
What enzyme converts UDP-galactose to UDP-glucose?
|
4-epimerase
|
|
Marasmus: Clinical presentation
|
Tissue and muscle wasting, loss of subcutaneous fat, and variable edema
|
|
Hunter's Syndrome vs Hurler's Syndrome: Which GAGs' degradation is affected?
|
Both: Dermatan sulfate and Heparan sulfate
|
|
Anode: What does it contain?
|
Cations
|
|
Phosphofructokinase-1: What stimulates it?
|
AMP, Fructose-2,6-BP
|
|
Names of the steps in protein synthesis
|
1. Initiation 2. Elongation 3. Termination
|
|
This enzyme phosphorylates glucose with a low capacity.
|
Hexokinase (as opposed to glucokinase)
|
|
This enzyme phosphorylates glucose with low affinity.
|
Glucokinase (as opposed to hexokinase)
|
|
Pyruvate dehydrogenase deficiency: Presentation
|
Lactic acidosis and neurologic defects
|
|
What are Heinz bodies?
|
altered Hemoglobin precipitates within RBCs, found in G6PD deficiency
|
|
Lipoamide or lipoate: Which carries aldehydes?
|
Lipoamide
|
|
Define operator of gene expression
|
Site where repressors bind
|
|
How much ATP is produced by the citric acid cycle per molecule of acetyl coA?
|
12 ATP.
|
|
Anode: What does it attract?
|
Anions
|
|
Pyruvate kinase: What does it do?
|
Pyruvate kinase converts phosphoenolpyruvate to pyruvate, thereby producing two ATP.
|
|
Inhibitors of electron transport from Cytochrome b to Cytochrome C?
|
Antimycin A
|
|
In nucleic acids, what kind of substitution is a transition?
|
Transition = Identical type (Purine for purine or pyrimidine for pyrimidine)
|
|
This enzyme phosphorylates glucose and is not feedback inhibited.
|
Glucokinase (as opposed to hexokinase)
|
|
Cyanogen bromide cleaves peptides at which side of what residues?
|
C-terminal of methionine
|
|
This enzyme phosphorylates glucose with a high capacity.
|
Glucokinase (as opposed to hexokinase)
|
|
What is on the 5' end of a nucleotide
|
Triphosphate
|
|
Chymotrypsin cleaves peptides at which side of what residues?
|
C-terminal side of tyrosine, phenylalanine, and tryptophan residues
|
|
Cathode: What does it contain?
|
Anions
|
|
What type of bonds hold the phosphoryls together in ATP, and how much energy are the bonds worth?
|
Phosphoanhydride bonds are worth 7 kilocalories per mole (but only between the alpha and beta and the beta and the gamma)
|
|
What are the requirements of PEP carboxykinase?
|
GTP
|
|
Hunter's Syndrome vs Hurler's Syndrome: Corneal clouding?
|
Hunter's: No, Hurler's: Yes
|
|
Ethanol metabolism: Limiting reagent
|
NAD+
|
|
In what condition is nucleotide excision repair mutated?
|
Xeroderma pigmentosa (dry skin with melanoma and other cancers)
|
|
Where in the cell does the following occur: Gluconeogenesis
|
Pathway has steps in the mitochondria and in the cytoplasm
|
|
Role of A site in protein synthesis
|
A site holds incoming Aminoacyl tRNA.
|
|
Hunter's Syndrome vs Hurler's Syndrome: Aggressive behavior?
|
Hunter's: Yes, Hurler's: No
|
|
Where in the electron transport chain do NADH and FADH2 release their electrons?
|
Complex I
|
|
Refsum Disease: Pathophysiology
|
Inability to degrade phytanic acid, resulting in accumulation in plasma and tissues
|
|
What is this molecule an activated carrier of?: Coenzyme A
|
Acyl
|
|
What are the rate limiting steps of glycolysis?
|
1. Hexokinase (Glucose to G-6-P) 2. *Phosphofructokinase-1 (Fructose-6-P to Fructose-1,6-BP) 3. Pyruvate kinase (PEP to Pyruvate)
|
|
What inhibits pyruvate dehydrogenase?
|
1. NADH; 2. ATP; 3. Acetyl CoA
|
|
Where does the pentose phosphate pathway happen?
|
Cytoplasm of Red Blood Cells, and in lactating mammary glands, liver, and adrenal cortex (all sites of fatty acid or steroid synthesis except RBCs)
|
|
What is rotenone?
|
An electron transport inhibitor.
|
|
Phosphofructokinase-1: What inhibits it?
|
ATP, Citrate
|
|
What activated carriers carry: Acyl
|
1. Coenzyme A 2. Lipoamide
|
|
What toxin inhibits lipoic acid?
|
Arsenic
|
|
What are the requirements of PEP carboxykinase?
|
GTP
|
|
What are the main products of the pentose phosphate shunt and their uses?
|
1. NADPH (for fatty acid and steroid synthesis) 2. Ribose-5-phosphate (for nucleotide synthesis) 3. G3P and F6P (glycolytic intermediates)
|
|
Chondroitin Sulfate: Where found?/Distinguishing characteristic from other GAGs
|
Cartilage, tendons, ligaments, aorta. Most abundant GAG in body.
|
|
Keratan Sulfate: Where found?/Distinguishing characteristic from other GAGs
|
Found in cartilage proteoglycan aggregates with chondroitin sulfate, and in cornea. Most heterogeneous GAG.
|
|
What are Aschoff Bodies?
|
Central fibrinoid necrosis surrounded by reactive histiocytes
|
|
Where is the murmur best heard for patent ductus arteriosus?
|
Between the shoulder blades
|
|
What are two common findings in myocarditis?
|
Aschoff bodies Anitschkow Cells the two Russians
|
|
What organism is involved in Rheumatic Fever?
|
Group A Strept Step. pyogenes
|
|
What are five signs of Rheumatic fever?
|
Carditis, Migratory polyarthritis, Subcutaneous Nodules, Erythema Marginatum, Sydenham's Chorea
|
|
What are the three A's in Atrial Septal Defects?
|
Adults, Alcohol Fetal Syndrome, ALL from Down Syndrome
|
|
What two diseases have Mitral Valve Prolapse?
|
Marfan's Syndrome and Ehlers Danlos
|
|
What two diseases are involved w/ mucin-producing sterile vegetations?
|
tumors of colon and pancreas Marantic vegetations
|
|
What other pathogens cause myocarditis?
|
Borrelia (Lyme Dz), T. cruzi (Chagas), Tichinella spiralis (trichinosis)
|
|
What is the genetic problem in hypertrophic cardiomyopathy?
|
mutation in heavy chain of beta-myosin and troponins [AD]
|
|
What is the MC site of metastasis to cardiac tissue?
|
pericardium
|
|
What disease is associated with cardiac rhabdomyoma?
|
Tuberous Sclerosis
|
|
What is the pathogenesis of mitral valve prolapse?
|
increase/accumulation of dermatan sulfate
|
|
Classic Finding for: Soap bubble on x-ray
|
Giant cell tumor of bone
|
|
Classic Finding for: Cotton-wool spots
|
Chronic hypertension
|
|
Classic Finding for: Recurrent pulmonary Pseudomonas and S. aureus infections
|
Cystic fibrosis
|
|
Classic Finding for: Birbeck granules on EM
|
Histiocytosis X (eosinophilic granuloma)
|
|
Classic Finding for: Pseudorosettes
|
Ewing's sarcoma
|
|
Classic Finding for: Trousseau's sign
|
Visceral cancer, pancreatic adenocarcinoma (migratory thrombophlebitis), hypocalcemia (carpal spasm)
|
|
Classic Finding for: Wallenberg's syndrome
|
Posterior Inferior Cerebellar Artery thrombosis
|
|
Classic Finding for: Cerebriform nuclei
|
Mycosis fungoides (cutaneous T-cell lymphoma)
|
|
Classic Finding for: Rotor's syndrome
|
Congenital conjugated hyperbilirubinemia
|
|
Classic Finding for: Kimmelstiel-Wilson nodules
|
Diabetic nephropathy
|
|
Classic Finding for: Call-Exner bodies
|
Granulosa-theca cell tumor of the ovary
|
|
Classic Finding for: Nephritis + cataracts + hearing loss
|
Alport's syndrome
|
|
Classic Finding for: Arnold-Chiari malformation
|
Cerebellar tonsillar herniation
|
|
Classic Finding for: Baker's cyst in popliteal fossa
|
Rheumatoid arthritis
|
|
Classic Finding for: Hypertension + hypokalemia
|
Conn's syndrome
|
|
Classic Finding for: Diabetes insipidus + exophthalmos + lesions of the skull
|
Hand–Schüller–Christian disease (multifocal Langerhans cell histiocytosis)
|
|
Classic Finding for: Reinke crystals
|
Leydig cell tumor
|
|
Classic Finding for: Reid index (increased)
|
Chronic bronchitis
|
|
Classic Finding for: von Recklinghausen's disease of bone
|
Osteitis fibrosa cystica (?brown tumor?)
|
|
Classic Finding for: Russell bodies
|
Multiple myeloma
|
|
Classic Finding for: Schiller-Duval bodies
|
Yolk sac tumor
|
|
Classic Finding for: Sulfur granules
|
Actinomyces israelii
|
|
Classic Finding for: Gilbert's syndrome
|
Benign congenital unconjugated hyperbilirubinemia
|
|
Classic Finding for: Lewy bodies
|
Parkinson's disease
|
|
Classic Finding for: Renal cell carcinoma + cavernous hemangiomas + adenomas
|
von Hippel-Lindau disease
|
|
Classic Finding for: Eburnation
|
Osteoarthritis (polished, ivory-like appearance of bone)
|
|
Classic Finding for: Arachnodactyly
|
Marfan's syndrome
|
|
Classic Finding for: Pannus
|
Rheumatoid arthritis
|
|
Classic Finding for: Mallory bodies
|
Alcoholic liver disease
|
|
Classic Finding for: MLF syndrome (INO)
|
Multiple sclerosis
|
|
Classic Finding for: "Smudge cell"
|
CLL
|
|
Classic Finding for: Pick bodies
|
Pick's disease
|
|
Classic Finding for: Hyperphagia + hypersexuality + hyperorality + hyperdocility
|
Klüver–Bucy syndrome (amygdala)
|
|
Classic Finding for: Owl's eye
|
CMV
|
|
Classic Finding for:Klüver–Bucy syndrome
|
Bilateral amygdala lesions
|
|
Classic Finding for: Crigler-Najjar syndrome
|
Congenital unconjugated hyperbilirubinemia
|
|
Classic Finding for: Job's syndrome
|
Neutrophil chemotaxis abnormality
|
|
Classic Finding for: Spike and dome on EM
|
Membranous glomerulonephritis
|
|
Classic Finding for: Shwartzman reaction
|
Neisseria meningitidis
|
|
Classic Finding for: Charcot's triad
|
Multiple sclerosis (nystagmus, intention tremor, scanning speech), cholangitis (jaundice, RUQ pain, fever)
|
|
Classic Finding for: Bartter's syndrome
|
Hyperreninemia
|
|
Classic Finding for: Bernard-Soulier disease
|
Defect in platelet adhesion
|
|
Classic Finding for: Hand–Schüller–Christian disease
|
Chronic progressive histiocytosis
|
|
Classic Finding for: Gaucher's disease
|
Glucocerebrosidase deficiency
|
|
Classic Finding for: Homer Wright rosettes
|
Neuroblastoma
|
|
Classic Finding for: Brushfield's spots
|
Down syndrome
|
|
Classic Finding for: "Brown tumor" of bone
|
Hemorrhage causes brown color of osteolytic cysts: 1. Hyperparathyroidism 2. Osteitis fibrosa cystica (von Recklinghausen's disease)
|
|
Classic Finding for: Negri bodies
|
Rabies
|
|
Classic Finding for: Wermer's syndrome
|
MEN type I
|
|
Classic Finding for: Sipple's syndrome
|
MEN type IIa
|
|
Classic Finding for: Bouchard's nodes
|
Osteoarthritis (PIP swelling 2º to osteophytes)
|
|
Classic Finding for: Subepithelial humps on EM
|
Poststreptococcal glomerulonephritis
|
|
Classic Finding for: Caisson disease
|
Gas emboli
|
|
Classic Finding for: Charcot-Leyden crystals
|
Bronchial asthma (eosinophil membranes)
|
|
Classic Finding for: Sézary's syndrome
|
Cutaneous T-cell lymphoma
|
|
Classic Finding for: Cowdry type A bodies
|
Herpesvirus
|
|
Classic Finding for: Fanconi's syndrome
|
Proximal tubular reabsorption defect
|
|
Classic Finding for: Intussusception
|
Adenovirus (causes hyperplasia of Peyer's patches)
|
|
Classic Finding for: Boutonniere deformity
|
Rheumatoid arthritis
|
|
Classic Finding for: Lisch nodules
|
Neurofibromatosis (von Recklinghausen's disease)
|
|
Classic Finding for: von Recklinghausen's disease
|
Neurofibromatosis with Café au lait spots
|
|
Classic Finding for: Xerostomia + arthritis + keratoconjunctivitis sicca
|
Sjögren's syndrome
|
|
Classic Finding for: Suboccipital lymphadenopathy
|
Rubella
|
|
Classic Finding for: Albuminocytologic dissociation
|
Guillain–Barré syndrome (↑ protein in CSF with only modest ↑ in cell count)
|
|
Classic Finding for: Heberden's nodes
|
Osteoarthritis (DIP swelling 2º to osteophytes)
|
|
Classic Finding for: HbF
|
Thalassemia major
|
|
Classic Finding for: Donovan bodies
|
Granuloma inguinale
|
|
Classic Finding for: Howell-Jolly bodies
|
Splenectomy (or nonfunctional spleen)
|
|
Classic Finding for: Curschmann's spirals
|
Bronchial asthma (whorled mucous plugs)
|
|
Classic Finding for: Councilman bodies
|
Toxic or viral hepatitis
|
|
Classic Finding for: Cold agglutinins
|
Mycoplasma pneumoniae, infectious mononucleosis
|
|
Classic Finding for: Albright's syndrome
|
Polyostotic fibrous dysplasia, precocious puberty, Café au lait spots, short stature, young girls
|
|
What four things arise from surface ectoderm?
|
1. Adenohypophysis, 2. Lens of eye, 3. Epithelial linings, 4. Epidermis
|
|
What ear muscle does the 1st branchial arch form?
|
Tensor tympani
|
|
What four structures make up the diaphragm?
|
1.Septum transversum; 2.Pleuroperitoneal folds; 3.Body wall; 4.Dorsal mesentery of esophagus
|
|
Does the serous linings of body cavities arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Mesoderm
|
|
What is the male homologue to the greater vestibular glands (of Bartholin) in the female?
|
Bulbourethral glands (of Cowper)
|
|
What are the 4th and 6th branchial arch derivatives innervated by?
|
CN X
|
|
What is the female homologue to the ventral shaft of the penis in the male?
|
Labia minora
|
|
The right common cardinal vein and right anterior cardinal vein give rise to what adult heart structure?
|
Superior vena cava
|
|
What are the 1st branchial arch derivatives innervated by?
|
CN V2 and V3
|
|
Which muscles (8) are derivatives of the 1st branchial arch?
|
-Temporalis-Masseter-Lateral pterygoid-Medial pterygoid-Mylohyoid-Anterior belly of digastric-Tensor tympani-Tensor veli palatini
|
|
Which two embryonic tissues are branchial arches derived from?
|
Mesoderm and neural crests
|
|
Which week of fetal development have the genitalia taken on male/female characteristics?
|
Week 10
|
|
What is oligohydramnios?
|
Less than 0.5 L of amniotic fluid
|
|
Which branchial arch does Meckel's cartilage develop from?
|
1st arch
|
|
What suppresses the development of the paramesonephric ducts in males?
|
Mullerian inhibiting substance (secreted by the testes)
|
|
How does a cleft lip form?
|
Failure of fusion of the maxillary and medial nasal processes
|
|
Does the pia arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Neural Crest (Ectoderm)
|
|
When do primary oocytes begin meiosis I?
|
During fetal life
|
|
Which branchial arch forms the incus and malleus of the ear?
|
1st arch
|
|
Which pharyngeal arch does Reichert's cartilage develop from?
|
2nd arch
|
|
Is a secondary spermatocyte N or 2N?
|
2N
|
|
What five things arise from neuroectoderm?
|
-Neurohypophysis-CNS neurons-Oligodendrocytes-Astrocytes-Pineal gland
|
|
What is polyhydramnios?
|
Greater than 1.5-2 L of amniotic fluid
|
|
Meiosis II is arrested in which phase until fertilization?
|
Metaphase (an egg MET a sperm)
|
|
What is a urachal cyst or sinus a remnant of?
|
The allantois
|
|
What is associated with an epispadias?
|
Exstrophy of the bladder
|
|
What is the normal remnant of the thyroglossal duct?
|
Foramen cecum
|
|
What is the flagellum (tail) derived from?
|
One of the centrioles
|
|
What are the cartilage derivatives (5) of the 4th and 6th branchial arches?
|
-Thyroid-Cricoid-Arytenoids-Corniculate-Cuneiform
|
|
What four things does Reichert's cartilage (from the 2nd arch) develop into?
|
-Stapes-Styloid process-Lesser horn of hyoid-Stylohyoid ligament
|
|
What four things does the dorsal pancreatic bud become?
|
Body, Tail, Isthmus, and Accessory Pancreatic Duct
|
|
From what does the ligamentum teres hepatis arise?
|
Umbilical vein
|
|
What does the 5th pharyngeal pouch develop into?
|
C cells of the thyroid
|
|
How long does full development of spermatogenesis take?
|
2 months
|
|
What induces the ectoderm to form the neuroectoderm (neural plate)?
|
Notochord
|
|
What fetal landmark has occurred within week 3 of fertilization?
|
Gastrulation
|
|
Which muscles (4) are derivatives of the 2nd branchial arch?
|
-Muscles of facial expression-Stapedius-Stylohyoid-Posterior belly of digastric
|
|
What is the female homologue to the corpus spongiosum in the male?
|
Vestibular bulbs
|
|
Do the urogenital structures arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Mesoderm
|
|
Is a spermatid haploid or diploid?
|
Haploid, N
|
|
What four things does the mesonephric (wolffian) duct develop into?
|
-Seminal vesicles-Epididymis-Ejaculatory duct-Ductus deferens
|
|
Is a speratogonium haploid or diploid?
|
Diploid, 2N
|
|
What type of twins would have 2 amniotic sacs and 2 placentas?
|
Monozygotic or dizygotic twins
|
|
What three things does the paramesonephric (mullerian) duct develop into?
|
-Fallopian tube-Uterus-Part of the vagina
|
|
What does the 4th pharyngeal pouch develop into?
|
Superior parathyroids
|
|
What connects the thyroid diverticulum to the tongue?
|
The thyroglossal duct
|
|
What type of twins would have 1 placenta, 2 amniotic sacs, and 1 chorion?
|
Monozygotic twins
|
|
How does a cleft palate form?
|
Failure of fusion of the lateral palatine processes, the nasal septum, and/or the median palatine process
|
|
When does fetal erythropoiesis occur in the liver?
|
Weeks 6-30
|
|
Which two branchial arches form the posterior 1/3 of the tongue?
|
3rd and 4th arches
|
|
What is the male homologue to the glans clitoris in the female?
|
Glans penis (all from Genital tubercle)
|
|
Which muscles are derivatives of the 6th branchial arch?
|
All intrinsic muscles of the larynx, except the cricothyroid
|
|
Is a secondary spermatocyte haploid or diploid?
|
Haploid, 2N
|
|
What does the 6th aortic arch give rise to?
|
The proximal part of the pulmonary arteries and (on left only) ductus arteriosus
|
|
What does the ligamentum venosum come from?
|
Ductus venosus
|
|
What is the female homologue to the scrotum in the male?
|
Labia majora (all from Labioscrotal swelling)
|
|
What four things does Meckel's cartilage (from the 1st arch) develop into?
|
-Mandible-Malleus-Incus-Sphenomandibular ligament
|
|
Which branchial arch forms the anterior 2/3 of the tongue?
|
1st arch
|
|
What does aberrant development of the 3rd and 4th pouches cause?
|
DiGeorge's syndrome
|
|
What is the food supply of sperm?
|
Fructose
|
|
What embryonic structure are the smooth parts of the left and right ventricle derived from?
|
Bulbus cordis
|
|
What embryonic structure does the coronary sinus come from?
|
Left horn of the sinus venosus
|
|
Which ear bone(s) does the 2nd branchial arch form?
|
Stapes
|
|
What is the female homologue to the prostate gland in the male?
|
Urethral and paraurethral glands (of Skene)
|
|
What fetal landmark has developed within week 2 of fertilization?
|
Bilaminar disk
|
|
What does the right 4th aortic arch give rise to?
|
Proximal part of the right subclavian artery
|
|
What does the 2nd pharyngeal pouch develop into?
|
Epithelial lining of the palantine tonsils
|
|
Does the thyroid arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Endoderm
|
|
What three things does the ventral pancreatic bud become?
|
-Pancreatic head-uncinate process-main Pancreatic duct
|
|
What does the thyroid diverticulum arise from?
|
The floor of the primitive pharynx
|
|
What is the acrosome of sperm derived from?
|
Golgi apparatus
|
|
Meiosis I is arrested in which phase until ovulation?
|
Prophase
|
|
When do primary oocytes complete meiosis I?
|
Just prior to ovulation
|
|
What can be found in the medulla of the thymus?
|
It is pale with mature T cells, epithelial reticular cells, and Hassall's corpuscles
|
|
What does the first branchial cleft develop into?
|
The external auditory meatus
|
|
The stapedius muscle of the ear is formed by which branchial arch?
|
2nd
|
|
Which muscles (3) are derivatives of the 4th branchial arch?
|
-Most pharyngeal constrictors-Cricothyroid-Levator veli palatini
|
|
Where does positive and negative selection occur in the thymus?
|
At the corticomedullary junction
|
|
Does the adrenal cortex arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Mesoderm
|
|
What does the 5th aortic arch give rise to?
|
Nothing
|
|
What teratogenic agent causes limb defects ('flipper' limbs)?
|
Thalidomide
|
|
Which branchial arch are the greater horn of hyoid and the stylopharyngeus muscle derived from?
|
3rd branchial arch
|
|
What does the 3rd aortic arch give rise to?
|
Common carotid artery and proximal part of the internal carotid artery
|
|
What does the umbilical arteries give rise to?
|
Medial umbilical ligaments
|
|
What fetal landmarks (2) have developed within week 3 of fertilization?
|
Primitive streak and neural plate begin to form
|
|
Does the dura connective tissue arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Mesoderm
|
|
Does the parathyroid arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Endoderm
|
|
What type of bone formation is spontaneous without preexisting cartilage?
|
Intramembranous
|
|
Do the odontoblasts arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Neural Crest (Ectoderm)
|
|
Do the parafollicular (C) cells of the thyroid arise from neural crest (ectoderm), mesoderm, or endoderm?
|
Neural Crest (Ectoderm)
|
|
What developmental contributions does the 5th branchial arch make?
|
None
|
|
Which aortic arch does the stapedial artery and the hyoid artery come from?
|
2nd aortic arch
|
|
What is Meckel's diverticulum?
|
Persistence of the vitelline duct or yolk sac
|
|
What are the 3rd branchial arch derivatives innervated by?
|
CN IX
|
|
What embryonic structure does the median umbilical ligament come from?
|
Allantois (urachus)
|
|
What fetal landmark has occurred within week 1 of fertilization?
|
Implantation
|
|
What can a persistent cervical sinus lead to?
|
A branchial cyst in the neck
|
|
What effect does 13-cis-retinoic acid have on the fetus?
|
Extremely high risk for birth defects
|
|
Is a primary spermatocyte haploid or diploid?
|
Diploid, 4N
|
|
What do the 2nd - 4th branchial clefts form, which are obliterated by proliferation of the 2nd arch mesenchyme?
|
Temporary cervical sinuses
|
|
What three things does the 1st pharyngeal pouch develop into?
|
-Middle ear cavity-Eustachian tube-Mastoid air cells
|
|
What is produced by delta cells of the Islets of Langerhans?
|
delta cells produce somatostatin.
|
|
IN what area of the spleen are B cells found?
|
B cells are found within the white pulp of the spleen.
|
|
What is the space of Disse?
|
Pores in liver sinusoids allowing plasma macromolecules access to liver cell surfaces.
|
|
What is the most common organism causes esophagitis?
|
Candida
|
|
What is the function of liver sinusoids?
|
Allow macromolecules of plasma full access to surface of liver cells through space of Disse.
|
|
What part of the stomach is affected by pernicious anemia?
|
Body and Fundus
|
|
Why is myasthemia gravis on the upper esophagus?
|
Upper 1/3 of esophagus is striated muscle
|
|
What is the most common congenital esophageal disorder?
|
Tracheoesophageal fistula
|
|
What is the pathogenesis of achalasia?
|
Failure of relaxation of LES sphincter
|
|
What is weakness in the esophageal wall called?
|
Zenker's Diverticulum
|
|
What is the name of the RUPTURE of the DISTAL esophagus?
|
Boerhaave's Sx
|
|
Why is there black melena?
|
Acid acts on HB and converts it into Hematin;Hematin is black pigment that stains fecal matter
|
|
What is a picture of a stomach that is really hard petrified almost?
|
Linitis plastica; Stomach Cancer diffuse type
|
|
What is the MC extranodal site of extranodal lymphoma?
|
stomach
|
|
What is the 2nd MC extranodal site of extranodal lymphoma?
|
peyer's patches
|
|
What is the MC benign tumor of GI tract?
|
Leiomyoma
|
|
What is the MC location for Leiomyoma in GI tract?
|
stomach
|
|
What is the main symptom of leiomyoma?
|
bleeding
|
|
What is the best test to detect Celiac Dz?
|
anti-gliadin Ab
|
|
What is the pathology of Celiac Dz?
|
Atrophy of villi in Duodenum and Jejunum
|
|
What is the pathology of Whipple's Dz?
|
blunting of villi in jejunum and ileum
|
|
What is the best (cheapest) screening test to determine malabsorption problem?
|
stool for fat
|
|
What is the best test for invasive diarrhea?
|
fecal leukocytes (+)
|
|
What is the #1 organism in invasive enterocolitis?
|
Campylobacter
|
|
What diarrhea's are low volume?
|
Invasive diarrhea
|
|
What diarrhea is high volume?
|
secretory and osmotic
|
|
What is secretory diarrhea?
|
high volume w/ osmolality similar to plasma
|
|
What is osmotic diarrhea?
|
high volume w/ osmolality lower than that of plasma
|
|
What are some disease that cause secretory diarrhea?
|
Vibrio cholerae (via adenylate cyclase); E. coli (via guanylate cyclase); Rotavirus, Carcinoid Sx
|
|
Is there mucosal inflammation in secretory diarrhea?
|
No mucosal inflammation
|
|
What is the MCC of diarrhea, cholecystitis and pancreatitis in AIDS?
|
Cytomelagolvirus (CMV)
|
|
What is the MCC of diarrhea in AIDS?
|
Cryptosporidium parvum
|
|
What test is used to detect Cryptosporidium parvum?
|
String Test
|
|
What organism causes rectal prolapse in children?
|
Trichuris trichura
|
|
What is the Tx of Trichuris trichura?
|
Albendazol
|
|
What is the reservoir of diphyllobothrium latum?
|
fish--- lake trout
|
|
What is the Tx fro D. latum?
|
praziquantel
|
|
What is seen in the stool of Strongyloides stercoralis?
|
rhabditiform larvae
|
|
What parasite in the soil penetrates the skin?
|
Strongyloides stercoralis
|
|
What is the MCC of hematochezia?
|
Diverticulosis
|
|
What is the 2nd MCC of hematochezia?
|
angiodysplasia
|
|
What is associated w/ angiodysplasia?
|
von Willebrand's Dz; Aortic Stenosis
|
|
What is the MCC of iron deficiency in newborn?
|
Mecke's Diverticulum; bleeding GI
|
|
What disease has the term left sided apendicitis?
|
sigmoid diverticula
|
|
What is the MCC of fistulas in the GI tract?
|
diverticula
|
|
What is the MC fistula?
|
Colovesical Fistula
|
|
What layers does UC comprise?
|
musocal and submucosal
|
|
What is involved in Cronh's Dz in 80%?
|
Terminal Ileum Affected
|
|
What is the marker that the patient will recover from HBV?
|
HBV-DNA poymerase leaves before HBsAg
|
|
Markers for HBV infection is active?
|
HBe and HBV-DNA antigens are excellent markers of infectivity
|
|
What marker for HBV determines a chronic carrier?
|
HBsAg for more than 6 months
|
|
What is a healthy carrier?
|
carries HBsAg but is negative for HBeAg/HBV-DNA
|
|
What organism causes spontaneous peritonitis in adults?
|
E. coli
|
|
What organism causes spontaneous peritonitis in children?
|
Step. pneumoniae
|
|
What causes a single abscess in the right lobe of the liver?
|
E. histolytica
|
|
Tx for Hepatic Amebiasis?
|
Metronidazole
|
|
Who is the definitive host of Echinococcosis?
|
Sheep Dog
|
|
Humans are what type of host for Echinococcosis?
|
intermediate host
|
|
Tx for Echinococcosis?
|
Albendazole
|
|
What organism causes cholangiocarcinoma?
|
Clonorchis sinensis
|
|
What is the Tx of Clonorchiasis?
|
Praziquantel
|
|
What is the main characteristic in the laboratory of Clonorchiasis?
|
Eosinophilia
|
|
What parasite causes portal hypertension, hepatosplenomegaly, ascites and esophageal varices?
|
Schistosomiasis
|
|
What is the definitive host of Schistosoma mansoni?
|
Snails
|
|
Tx for Schistosomiasis?
|
Praziquantel
|
|
What is a cause of post-hepatic obstruction?
|
1) Budd-Chiari syndrome 2) Polycythemia vera 3) Oral Contraceptives
|
|
What is the MCC of post-hepatic obstruction?
|
Polycythemia vera!
|
|
Symmptoms of post-hepatic obstruction?
|
1) painful liver 2) congested liver 3) ascites 4) portal hypertension
|
|
What are dead hepatocytes called?
|
Councilman Bodies
|
|
When do we find Councilman Bodies?
|
Hepatitis
|
|
What alcoholic disease is irreversible?
|
cirrhosis
|
|
Are fatty change and alcoholic hepatitis reversible or irreversible?
|
reversible
|
|
What are the factors of Alcholo liver disease?
|
1) amount of EtOH 2) duration of intake 3) more damage in females
|
|
Where is the most important site of metabolism of EtOH in liver?
|
cytosol
|
|
Where is alcohol dehydrogenase found?
|
in cytosol and mitochondria
|
|
Why is there esteatosis in alcoholic patients?
|
alcohol is converted to acetaldehyde and acetate and acetyl coA which makes free fatty acids - increase in NADH2 favors glycerol-3-p
|
|
What is the sequence to make TG (VLDL) from 1,3 DPG?
|
1,3 DPG to Glyceraldehyde-3-P to DHAP to Glycerol-3-P + FA makes TG
|
|
Why is ketoacidosis sometimes present in alcoholics?
|
NADH once again favors conversion of: Acetoacetate to B-Hydroxybutyrate (ketoacids)
|
|
Why are alcoholics prone to gout?
|
Ketoacids and Lactic Acid compete w/ uric acid for excretion in the kidneys; so Uric Acid Accumulates!
|
|
What is the ratio of ALT and AST in alcoholics?
|
AST > ALT
|
|
What is seen in alcoholic hepatitis?
|
mallory bodies
|
|
What are the symptoms in obstructive jaundice?
|
-hypercholesterolemia-light colored stools-urine w/conjugated bilirubin-increase alkaline phosphatase (AP) and gamma-glutamyltransferas (GGT)
|
|
What are the symptoms of primary biliary cirrhosis?
|
-pruritus-increase AP and GGT-no jaundice until later
|
|
What disease causes primary slcerosing pericholangitis?
|
ulcerative colitis
|
|
What cancer is related to Primary sclerosing pericholangitis?
|
MCC of cholangiocarcinoma
|
|
Name drug that causes acute hepatitis? (4)
|
1) Isoniazid 2) Halothane 3) acetaminophen 4) methyldopa
|
|
Name two drugs that cause cholestasis?
|
1) oral contraceptives 2) anabolic steroids
|
|
What drugs cause steatosis? fatty liver? (2)
|
1) Amiodarone 2) Methotrexate
|
|
What drug causes fibrosis in the liver?
|
methotrexate
|
|
What drug causes angiosarcoma of the liver?
|
Vinyl Chloride
|
|
What drug causes Liver Cell Adenoma?
|
Oral Contraceptives
|
|
What drugs (3) causes hepatocellular carcinoma?
|
1) Vinyl Chloride 2) Aflatoxin (Aspergillus mold) 3) Thorotrast
|
|
Can O.C. cause hepatocellular CA?
|
Yes
|
|
What is fulminant hepatic failure (FHF)?
|
acute liver failure w/ encephalopathy within 8 weeks of hepatic dysfunction
|
|
What is the MCC of fulminant hepatic failure? (drug)
|
acetaminophen
|
|
What is the MCC of fulminant hepatic failure? (organism)
|
virus
|
|
Other cause of fulminant hepatic failure (except drug and organism)?
|
Reye's Sx
|
|
What are the laboratory findings of hemochromatosis?
|
- increase serum iron - decrease TIBC - increase % saturation - increase serum ferritin
|
|
What is the best screening test of hemochromatosis?
|
increase serum ferritin
|
|
What are the manifestations of hemochromatosis?
|
- bronze skin - pancreas (malabsorption and DM) - restrictive cardiomyopathy - liver anormalities including hepatocellular CA in 30%
|
|
What nuclei is attacked in Wilson's Dz?
|
lenticular nuclei degeneration
|
|
What are the symptoms of degeneration of the lenticular nuclei?
|
-chorea-rigidity-basal ganglia dementia
|
|
What part of the eye is affected w/ Kayser-Fleischer rings?
|
outer part of decemet; cornea
|
|
What disorder results from a lesion in the medial longitudinal fasciculus (MLF)?
|
Internuclear ophthalmoplegia (INO)
|
|
If you break your medial epicondyle of the humerus, which nerve would likely injure?
|
ulnar nerve
|
|
What lobe of the brain is the principal sensory area in?
|
parietal
|
|
What nerve is known as the great extensor nerve?
|
radial nerve
|
|
What are the functions of the major structures of the inner ear bony labyrinth?
|
1. Cochlea- hearing 2. vestibule- linear acceleration 3. semicircular canals- angular acceleration.
|
|
What CNS/ PNS supportive cell has the following functions: phagocytosis?
|
Microglia
|
|
CN V2 passes through what 'hole'?
|
foramen rotundum
|
|
Name the thenar muscles
|
--Opponens pollicis--Abductor pollicis brevis--Flexor pollicis brevis
|
|
What gut regions and structures does the celiac artery supply?
|
1.Foregut 2.--Stomach to duodenum --liver --gallbladder --pancreas
|
|
The hippocampus has input from what two areas?
|
Entorhinal cortex and Septal area
|
|
What 3 muscles are lost in a lesion of the musculocutaneous nerve?
|
coracobrachialis, biceps brachii, and brachialis
|
|
Name 2 locations for lesions in Syringomyelia?
|
ventral white commissure and ventral horns
|
|
What layer of the peripheral nerve must be rejoined in microsurgery for limb reattachment?
|
The perineurium must be rejoined in microsurgery for limb reattachment.
|
|
What defect may predispose an infant for a diaphragmatic hernia?
|
Defective development of the pleuroperitoneal membrane
|
|
What 2 symptoms are seen with a lesion of the ulnar nerve?
|
Weak intrinsic muscles of the hand and Pope's blessing
|
|
What bone do all the foramina of the middle cranial fossa pass through?
|
sphenoid bone
|
|
What are the major structures of the inner ear membranous labyrinth?
|
1. Cochlear duct 2. utricle. 3. saccule 4. semicircular canals.
|
|
CN IX has what 4 functions?
|
posterior 1/3 taste, swallowing, salivation (parotid), monitoring carotid body and sinus
|
|
What is the consequence when your CNS stimulates the gamma motor neuron and the intrafusal fibers contract?
|
increased sensitivity of the reflex arc
|
|
What structures make up the bronchopulmonary segment?
|
Tertiary bronchus, Bronchial artery, and Pulmonary artery
|
|
Name the 4 foramina that are in the posterior cranial fossa?
|
internal auditory meatus, jugular foramen, hypoglossal canal, and foramen magnum.
|
|
The xiphoid process exists in what dermatome?
|
T7
|
|
What layers of the gut wall contribute to support (3)?
|
--Serosa--Lamina propria--Submucosa
|
|
The Nucleus Ambiguus has fibers from what 3 CNs?
|
CN IX, X, XI
|
|
What 4 structures pass through the jugular foramen?
|
CN IX, X, XI(descending), jugular vein
|
|
What would happen if you lesioned your ventromedial nucleus of the hypothalamus?
|
have hyperphagia and become obese
|
|
The umbilicus exists in what dermatome?
|
T10
|
|
What are the input and output of the anterior nucleus of the thalamus?
|
input - mammillary body, output - cingulate gyrus
|
|
What layers of the gut wall contribute to motility (4)?
|
--Muscularis mucosae--Inner circular muscle layer--Myenteric plexus--Outer longitudinal muscle layer
|
|
Brodmann's area 4 is?
|
principal motor area
|
|
What reflex is lost in a lesion of the musculocutaneous nerve?
|
biceps reflex
|
|
What structure passes through the foramen rotundum?
|
CN V2
|
|
What structures are in the carotid sheath?
|
Internal Jugular Vein (lateral), Common Carotid Artery (medial) and Vagus Nerve (posterior)
|
|
Common peroneal, Tibial, Femoral, and Obturator nerves arise from what spinal cord segments (4 answers)?
|
--'L4-S2 (common peroneal) --L4-S3 (tibial) --L2-L4 (femoral) and (obturator)
|
|
A lesion of the Striatum can cause which 2 diseases?
|
Huntington's and Wilson's disease
|
|
A lesion of the right optic tract produces?
|
left homonymous hemianopsia
|
|
An aneurysm of what artery may cause CN III palsy?
|
posterior communicating artery
|
|
Bell's Palsy is seen as a complication in what 5 things?
|
AIDS, Lyme disease, Sarcoidosis, Tumors, Diabetes (ALexander Bell with STD)
|
|
What two bones do all the foramina of the posterior cranial fossa pass through?
|
temporal and occipital bones
|
|
CN III has what 4 functions?
|
eye movement, pupil constriction, accommodation, eyelid opening
|
|
Brodmann's area 17 is?
|
principal visual cortex
|
|
What 5 types of cells make up the suportive cells of the CNS/PNS?
|
Astrocytes, Microglia, Oligodendroglia, Schwann cells, Ependymal cells.
|
|
CN VII has what 4 functions?
|
facial movement, anterior 2/3 taste, lacrimation, salivation(SL, SM glands)
|
|
Brodmann's area 41, 42 is?
|
primary auditory cortex
|
|
What nerve innervates the muscles that close and open the jaw?
|
Trigeminal Nerve (V3)
|
|
What muscle sensor senses tension and provides inhibitory feedback to alpha motor neurons?
|
golgi tendon organs
|
|
What is Endoneurium?
|
Endoneurium invests single nerve fiber of the peripheral nerve.
|
|
Give 4 characteristics of an UMN lesion.
|
spastic paralysis, increased deep tendon reflexes, + Babinski, minor to no atrophy
|
|
What CNS/ PNS supportive cell has the following functions: physical support, repair, K+ metabolism?
|
Astrocytes
|
|
What structures do the broad ligament contain (4)?
|
Round ligaments of the uterus, Ovaries, Uterine tubules and Uterine vessels
|
|
The Blood-Brain Barrier is formed by what 3 structures?
|
Choriod Plexus Epithelium, Intracerebral Capillary Endothelium, Astrocytes
|
|
Which thalamic nucleus has the function of body senses(proprioception, pressure, pain, touch, vibration)?
|
Ventral Posterior Lateral Nucleus (VPL)
|
|
Which way does the jaw deviate in a unilateral lesion (LMN) of CN V? (toward or away)
|
toward the lesion
|
|
How does the course of the left recurrent laryngeal nerve differ from that of the right?
|
The left wraps around the arch of the aorta and the ligamentum arteriosum while the right wraps around the subclavian artery.
|
|
Which thalamic nucleus has the function of facial sensation and pain?
|
Ventral Posterior Medial Nucleus (VPM)
|
|
What 3 muscles are lost in a lesion of the radial nerve?
|
triceps brachii, brachioradialis, and extensor carpi radialis longus
|
|
Traction or tear of the superior trunk of the brachial plexus causes what syndrome?
|
Erb-Duchenne palsy (waiter's tip)
|
|
The central retinal artery is a branch off what larger artery?
|
Ophthalmic Artery
|
|
What nerve innervates most of the 'palat' muscles and which is the exception?
|
All muscles with root 'palat' in their names (except tensor veli palatini, innervated by V2) are innervated by vagus nerve.
|
|
What syndrome is seen with a lesion of the lower trunk of the brachial plexus?
|
Claw hand
|
|
Name two proteins involved in the structure of zona adherens?
|
1. E-cadherins 2. actin filaments
|
|
Golgi tendon organs send their signal via what nerve?
|
group Ib afferents
|
|
A pudendal nerve block is performed at what landmark?
|
Ischial spine
|
|
The male sexual response of ejaculation is mediated by what part of the nervous system?
|
Visceral and somatic nerves
|
|
Subarachnoid space extends to what spinal level?
|
S2
|
|
What part of the spinal cord is spared with complete occlusion of the ventral artery?
|
dorsal columns
|
|
What structure passes through the foramen ovale?
|
CN V3
|
|
What passes through the cavernous sinus? (nerves and artery)
|
CN III, IV, V1, V2, VI, post-ganglionic SNS and the Internal carotid artery
|
|
What syndrome is seen with a lesion of the posterior cord of the brachial plexus?
|
Wrist drop
|
|
CN I passes through what 'hole'?
|
cribriform plate
|
|
Where is the lesion in a patient with hemiballismus?
|
Subthalamic nucleus
|
|
Obturator nerve damage manifests what deficit?
|
Loss of hip adduction
|
|
What are the input and output of the mammillary body?
|
input - hippocampal formation, output - anterior nucleus of the thalamus
|
|
The male sexual response of erection is mediated by what part of the nervous system?
|
Parasympathetic nervous system
|
|
What is the name for the small muscle fiber type that regulates muscle length?
|
Intrafusal fibers
|
|
What 2 cutaneus nerves are lost in a lesion of the radial nerve?
|
Posterior brachial cutaneous and posterior antebrachial cutaneous
|
|
What vagal nuclei controls motor innervation to the pharynx, larynx, and upper esophagus?
|
Nucleus Ambiguus (Motor=aMbiguus)
|
|
What muscle fiber type makes up the muscle bulk and provides the force for contraction?
|
Extrafusal fibers
|
|
What symptom is seen with a lesion of the median nerve?
|
decreased thumb function
|
|
What muscle extorts, elevates, and adducts the eye?
|
inferior oblique
|
|
A lesion of the right visual fibers just prior to the visual cortex produces?
|
left hemianopsia with macular sparing
|
|
Which ligament contains the uterine vessels?
|
Transverse cervical (cardinal) ligament
|
|
From which 3 spinal roots does long thoracic nerve arises?
|
C5, C6, C7
|
|
Vertigo, ataxia, visual deficits, and coma are caused by stroke of the? (ant. circle or post. circle)
|
Posterior circle
|
|
What is affected in a central VII lesion (lesion above the facial nucleus - UMN)?
|
paralysis of the contralateral lower quadrant
|
|
What 4 areas is there decreased output in Parkinson's?
|
substantia nigra pars compacta, globus pallidus, ventral anterior nucleus, cortex
|
|
Where in the inner ear are the ampullae found? What is the function of this structure?
|
Semicircular canals contain ampullae. Functions in detecting angular acceleration.
|
|
General sensory/motor dysfunction and aphasia are caused by stroke of the? (ant. circle or post. circle)
|
anterior circle
|
|
What lesion produces sensory(fluent/receptive) aphasia with poor comprehension?
|
Wernicke's area (associative auditory cortex)
|
|
What is the membranous labyrinth filled with? Describe its composition.
|
The membranous labyrinth is filled with endolymph. Endolymph is K+ rich, similar to ICF.
|
|
What is a hiatal hernia?
|
Stomach contents herniate upward through the esophageal hiatus of the diaphragm
|
|
What 2 spinal roots make up the superior trunk of the brachial plexus?
|
C5, C6
|
|
Give 3 charateristics of internuclear ophthalmoplegia (INO)
|
medial rectus palsy on lateral gaze, nystagmus in abducted eye, normal convergence.
|
|
What 4 movements are impaired in a lesion of the ulnar nerve?
|
wrist flexion, wrist adduction, thumb adduction, and adduction of the 2 ulnar fingers
|
|
In a lesion of the radial nerve, what muscle is associated with wrist drop?
|
extensor carpi radialis longus
|
|
Name two proteins involved in the structure of macula adherens.
|
1. Desmoplakin 2.Keratin
|
|
Intrafusal fibers are innervated by what motor neuron?
|
gamma motor neuron
|
|
If you break your surgical neck of the humerus, which nerve would likely injure?
|
axillary nerve
|
|
How are the fibers of the spinothalmic tract laminated? (sacral/cervical medial or lateral?)
|
cervical-medial, sacral-lateral
|
|
If you break your supracondyle of the humerus, which nerve would likely injure?
|
median nerve
|
|
Brodmann's area 22 is?
|
Wernicke's area (associative auditory cortex)
|
|
If you break your humerus mid-shaft, which nerve would likely injure?
|
radial nerve
|
|
Brodmann's area 6 is?
|
premotor area
|
|
What lesion produces coma?
|
reticular activating system
|
|
What artery do the lateral striate branch off of?
|
internal carotid artery
|
|
What artery does the anterior spinal artery branch off of?
|
vertebral artery
|
|
What 4 movements are lost in a lesion of the median nerve?
|
forearm pronation, wrist flexion, finger flexion, and several thumb movements
|
|
The infraorbital nerve is a branch off what larger nerve?
|
CN V2
|
|
What lesion produces spatial neglect syndrome?
|
right parietal lobe -- contralateral neglect.
|
|
What are the input and output of the entorhinal cortex?
|
input - cingulate gyrus, output - hippocampal formation
|
|
What are the input and output of the cingulate gyrus?
|
input - anterior nucleus of the thalamus, output - entorhinal cortex
|
|
Horner's Syndrome is present if the lesion in Brown-Sequard is above what level?
|
T1
|
|
What artery does the superior cerebellar artery branch off of?
|
basilar artery
|
|
An aneurysm of the anterior communicating artery may cause what type of defects?
|
visual defects
|
|
What part of pancreas are the Islets of Langerhans concentrated?
|
Islets of Langerhans are most numerous in the tail of pancreas.
|
|
Extrafusal fibers are innervated by what motor neuron?
|
alpha motor neuron
|
|
If the radial nerve is lesioned, what 2 reflexes are lost?
|
triceps reflex and brachioradialis reflex
|
|
Beginning with anterior communicating artery describe the path around the circle of Willis.
|
ant. comm. - ACA - ICA - post. comm. - PCA - PCA - post. comm. - ICA - ACA - ant. comm.
|
|
Where is the Submucosal plexus located?
|
Between mucosa and inner layer of smooth muscle in GI tract wall.
|
|
What happens if a swinging light test is performed on a Marcus Gann pupil (afferent pupil defect)?
|
results in pupil dialation of the defective eye as the light is swung from the normal eye to the defective eye
|
|
What syndrome is seen with a lesion of the radial nerve?
|
Saturday night palsy
|
|
What structures perforate the diaphragm at what vertebral levels?
|
IVC at T8, Esophagus and Vagal trunks at T10, and Aorta, Thoracic duct, and Axygous vein at T12 ?I 8 10 Eggs At 12?
|
|
What are the input and output of the septal area?
|
input - hippocampal formation, output - hippocampal formation
|
|
What vagal nuclei controls visceral sensory in formation like taste and gut distention?
|
Nucleus Solitarius (Sensory=Solitarius)
|
|
Where is the lesion in Parkinson's?
|
Substantia nigra pars compacta
|
|
What would happen to temperature regulation if you lesioned your posterior hypothalamus?
|
lose the ability to conserve heat
|
|
What CN arises dorsally?
|
CN IV trochlear
|
|
The male sexual response of emission is mediated by what part of the nervous system?
|
Sympathetic nervous system
|
|
Which thalamic nucleus is the primary motor cortex?
|
Ventral Lateral Nucleus (VL)
|
|
Which CNs pass through the middle cranial fossa?
|
CN II - VI
|
|
The inguinal ligament exists in what dermatome?
|
L1
|
|
The hippocampal formation is connected to the mammillary body and septal area via what structure?
|
Fornix
|
|
A lesion of the globus pallidus causes what disease?
|
Wilson's disease
|
|
What makes endolymph?
|
Endolymph is made by the stria vascularis.
|
|
What CNs lie medially at the brain stem?
|
CN III, VI, XII (3 - 6 - 12)
|
|
What do the medullary cords consist of?
|
Closely packed lymphocytes and plasma cells.
|
|
What 1 nerve root is assoc. with the biceps reflex?
|
C5
|
|
What are the major structures of the inner ear bony labyrinth?
|
1. Cochlea 2. vestibule 3. semicircular canals
|
|
What muscle opens the jaw?
|
Lateral pterygoid
|
|
Name 3 locations for lesions in Vit.B12 neuropathy(Friedreich's ataxia)?
|
dorsal columns, lateral corticospinal tracts, and spinocerebellar tracts
|
|
What are the 3 layers of peripheral nerves? (inner to outer)
|
Endoneurium, Perineurium and Epineurium
|
|
Neurons from the striatum have what action on the globus pallidus?
|
Inhibitory
|
|
Which thalamic nucleus has pre-motor function?
|
Ventral Anterior Nucleus (VA)
|
|
Erection and sensation of the penis is in what dermatomes?
|
S2-S4
|
|
Visual fibers from the lateral geniculate body terminate on the upper and lower banks of what fissure?
|
Calcarine fissure
|
|
What structure is in the femoral triangle but not in the femoral sheath?
|
The Femoral nerve
|
|
What 3 structures pass through the optic canal?
|
CN II, ophthalmic artery, central retinal vein
|
|
Neurons from the globus pallidus have what action on the ventral anterior nucleus?
|
Inhibitory
|
|
What lesion produces conduction aphasia, poor repetition w/ poor comprehension, and fluent speech?
|
Arcuate fasiculus
|
|
Name the type of movement with slow writhing movements (esp. the fingers)?
|
Athetosis
|
|
Which part of the cochlea picks up high frequency sound? Which picks up low frequency?
|
The base of the cochlea picks up high frequency sound the apex picks up low frequency sound
|
|
Name the hypothenar muscles.
|
--Opponens digiti minimi--Abductor digiti minimi--Flexor digiti minimi
|
|
What 1 nerve root is assoc. with the triceps reflex?
|
C7
|
|
What 2 spinal roots make up the inferior trunk of the brachial plexus?
|
C8, T1
|
|
What vagal nuclei sends parasympathetic fibers to the heart, lungs, and upper GI?
|
dorsal motor nucleus of CN X
|
|
A lesion of the right dorsal optic radiation (parietal lesion) produces?
|
left lower quadrantic anopsia (a temporal lesion)
|
|
Where in the inner ear are the maculae found? What is the function of this structure?
|
The utricle and saccule contain maculae Functions in detecting linear acceleration.
|
|
What is the function of hair cells?
|
Hair cells are the sensory elements in both the cochlear and vestibular apparatus.
|
|
The hippocampus has output to what two areas?
|
Mammillary body and Septal area
|
|
What type of lesion is seen in Werdnig-Hoffmann disease and is it genetic or acquired?
|
genetic LMN lesion causing flaccid paralysis (aka. Floppy infant disease)
|
|
The embryologic defect of having a cervical rib can compress what 2 structures?
|
Subclavian artery and Inferior trunk of the brachial plexus
|
|
Name the 4 ligaments of the uterus.
|
--Suspensory ligament of ovaries--Transverse cervical (cardinal) ligament--Round ligament of Uterus--Broad ligament
|
|
The Nucleus Solitarius has fibers from what 3 CNs?
|
CN VII, IX, X
|
|
What is Epineurium?
|
Epineurium (dense connective tissue) surrounds entire nerve (fascicles and blood vessels)
|
|
What 2 symptoms are seen with a lesion of the musculocutaneus nerve?
|
Difficulty flexing the arm and Variable sensory loss
|
|
Describe the outer structure of a Peyer's patch.
|
A Peyer's patch is 'covered' by single layer of cuboidal enterocytes, interspersed with specialized M cells (no goblet cells).
|
|
What muscle intorts, depresses, and abducts the eye?
|
superior oblique
|
|
A lumbar puncture is performed at what landmark?
|
Iliac crest
|
|
The recurrent laryngeal nerve arises from what cranial nerve and supplies what muscles?
|
1.CN X 2.All intrinsic muscles of the larynx except the cricothyroid muscle.
|
|
What spinal cord levels are vertebral disk herniation most likely to occur?
|
Between L5 and S1
|
|
What 4 'muscles' does the radial nerve innervate?
|
Brachioradialis, Extensors of the wrist and fingers, Supinator, Triceps. (BEST)
|
|
What nerve innervates most of the 'glossus' muscles and which is the exception?
|
All muscles with root 'glossus' in their names (except palatoglossus, innervated by vagus nerve) are innervated by hypoglossal nerve.
|
|
What muscular disorder is a medial longitudinal fasciculus syndrome associated with?
|
Multiple Sclerosis (MLF=MS)
|
|
Femoral nerve damage manifests what deficit?
|
Loss of knee jerk
|
|
What structures are pierced when doing an LP?
|
1.Skin/superficial fascia 2.Ligaments 3.Epidural space 4.Dura mater 5.Subdural space 6.Arachnoid 7.Subarachnoid space--CSF
|
|
How are the fibers of the corticospinal tract laminated? (legs/arms medial or lateral?)
|
arms- medial, legs-lateral
|
|
What 4 things do the lateral striate arteries supply?
|
internal capsule, caudate, putamen, globus pallidus
|
|
Why is the forearm pronated in Erb-Duchenne palsy?
|
loss of the biceps brachii
|
|
What is the most common circle of Willis aneurysm?
|
anterior communicating artery
|
|
What are 4 substances contained within the lysosomes of neutrophils?
|
Hydrolytic enzymes, Lysozyme, Myeloperoxidase, Lactoferrin
|
|
Which malaria is associated with nephrotic syndrome?
|
P. malariae
|
|
What is the most common malaria?
|
Vivax
|
|
Which malaria is the most lethal?
|
Falciparum
|
|
What specialized vascular structure is found in the lymph node paracortex? What is the function of this structure?
|
Paracortex contains high endothelial venules (HEV). T and B cells enter from the blood through the HEV.
|
|
What drug do you use for resistant falciparum?
|
Mefloquine
|
|
What does CD stand for?
|
cluster of differentiation
|
|
What are 3 morphological characteristics of monocytes?
|
Large, Kidney-shaped nucleus and Extensive 'frosted glass' cytoplasm
|
|
What percentage of leukocytes exist as neutrophils in the blood?
|
40 - 75%
|
|
What leukemia has gum infiltration?
|
Acute Monocytic Leukemia (M5)
|
|
What are the substances contained within the densely basophilic granules of the basophil? (4)
|
-Heparin (anticoagulant)-histamine (vasodilator)-vasoactive amines-Slow reacting substance of anaphylaxis
|
|
How do you treat falciparum malaria infection?
|
IV quinidine or quinine plus doxycycline
|
|
What kind of cells are found nearby the sinusoids of the spleen?
|
Macrophages
|
|
What do medullary sinuses consist of?
|
Medullary sinuses contain reticular cells and macrophages.
|
|
What do medullary sinuses communicate with?
|
Medullary sinuses communicate with efferent lymphatics.
|
|
Describe the histologic structure of sinusoids of the spleen.
|
Long, vascular channels in red pulp. With fenestrated 'barrel hoop' basement membrane.
|
|
What is the importance of the physiologic chloride shift in erythrocytes?
|
Membranes contain the chloride bicarbonate antiport allowing the RBC to transport carbon dioxide from the the lung periphery for elimination.
|
|
What is the frequency of acute leukemias?
|
Acute Myelogenous Leukemia (M2) 30-40% Acute Promyelocytic (M3) 5-10%, Acute Monocytic (M5) 10%
|
|
What is the treatment for all malarias except falciparum?
|
Chloroquine plus primaquine
|
|
What percentage of leukocytes exist as eosinophils in the blood?
|
1 - 6%
|
|
What is the basic morphology of an eosinophil? (2 things)
|
Bilobate nucleus and Packed with large eosinophilic granules of uniform size
|
|
What percentage of leukocytes in blood are monocytes?
|
2 - 10%
|
|
What does the American variant involve? (Burkitt's)
|
GI, ovaries and retroperitoneum
|
|
What is the Starry Sky?
|
macrophages w/ phagocytosed apoptotic bodies
|
|
What are Reed-Sternberg Cells?
|
transformed germinal center B cells
|
|
What CD maker's do you use to detect RS cells?
|
CD15 and CD30;
|
|
What factor involved in extrinsic pathway?
|
VII
|
|
What factor involved in intrinsic pathway?
|
XII, XI, IX, VIII
|
|
What is the best test for vWF diases?
|
ristocetin cofactor assay
|
|
What function does SIS have?
|
GF synthesis, (Growth Factor)
|
|
What fx does ERB-B2 has?
|
Receptor Synthesis
|
|
What fx does ABL has?
|
Non-receptor TK activity
|
|
What fx does RET have?
|
Receptor Synthesis
|
|
What fx does MYC have?
|
Nuclear Transcription
|
|
What fx does N-MYC have?
|
Nuclear transcription
|
|
What fx does RAS has?
|
GTP signal transduction
|
|
What two POC have the same function of Receptor Synthesis?
|
ERB-B2 and RET
|
|
What two POC have the same fx of nuclear transcription?
|
c-MYC and N-MYC
|
|
What does SIS activate by?
|
Overexpression
|
|
What does ERB-B2 activate by?
|
Amplification
|
|
What does RET Activate by?
|
Point Mutation
|
|
What does RAS activate by?
|
Point Mutation
|
|
What does ABL activate by?
|
translocation t(9;22)
|
|
What does MYC activate by?
|
c-MYC translocation t(8;14)
|
|
What does N-MYC activate by?
|
Amplification
|
|
What two POC amplify by?
|
ERB-B2 and N-MYC
|
|
What two POC activate by point mutation?
|
RET and RAS
|
|
What two POC activate by translocation?
|
ABL and c-MYC
|
|
What virus is associated w/ SIS POC and w/ Osteogenic Sarcoma?
|
EBV
|
|
What POC amplifies breasts??? imagine that...
|
ERB-B2
|
|
What are the inactivation of suppressor genes?
|
TP53, RB, APC and BRCA1/2
|
|
What suppressor gene (SG) is associated w/ lung, colon, breast and Li-Fraumeni syndrome?
|
TP53
|
|
What SG is associated w/ breast, ovary and prostate CA?
|
BRCA 1, BRCA 2
|
|
What SG is associated w/ familial polyposis: color cancer?
|
APC
|
|
What is the function of TP53?
|
G1 to S phase inhibitor
|
|
What is the function of BRCA 1/2 gene?
|
Regulates DNA repair
|
|
What is the APC gene function?
|
Prevents nuclear transcription, - degrades catenin; an activator of nuclear transcription
|
|
What is the function of RB gene?
|
G1 to S phase inhibitor
|
|
What are the genes of anti-apoptosis?
|
BCL-2 genes
|
|
What is the function of BCL-2 genes?
|
prevents the leakage of cytochrome c (signal for apoptosis)
|
|
What disease is associated with BCL-2?
|
b-cell lymphoma, Follicular Lymphoma t14;18
|
|
What is another disease that involves TP53?
|
Ataxia Telangiectasia, susceptibility to malignant lymphoma
|
|
What virus is associated w/ TP53?
|
HBV and HTLV-1(T cell leukemia and lymphoma), HPV 16,18 HPV16 inhibits TP53, RB inhibited by HPV 18
|
|
What carcinogen is implicated with pancreatic adenocarcinoma, SCC of oropharynx and upper/mid esophagus?
|
Alcohol
|
|
What carcinogen is implicated with colorectal cancer?
|
Lithocholic acid and Secondary bile acid
|
|
What carcinogen is implicated with Lung CA? (4)
|
Uranium, Asbestos, Chromium, and Nickel
|
|
What carcinogen is implicated with breast cancer and cervical cancer?
|
Oral Contraceptives
|
|
What carcinogen is implicated with SCC of skin, lung CA, liver angiosacroma?
|
Arsenic
|
|
What carcinogen is implicated with TCC of bladder? (2)
|
cyclophosphamide and b-naphthylamine (dye and rubber indus.)
|
|
What carcinogen is implicated with acute leukemia?
|
benzene
|
|
What carcinogen is implicated with SCC of scrotum?
|
tar, soot, oil (chimney sweeper)
|
|
What carcinogen is implicated with malignant lymphoma?
|
Alkylating agents
|
|
What is the most common risk factor for larynx CA?
|
polycyclic HOC (hydrocarbons)
|
|
What is the most common risk factor for pancreas?
|
polycyclic HOC
|
|
What is the most common risk factor for breast CA?
|
Age >50, excess estrogen: 1) nulliparity 2) early menarche 3) late menopause 4) obesity
|
|
What is the most common risk factor for dysgerminoma/gonadoblastoma?
|
Turner Sx XO dysgerminoma XO/XY gonadoblastoma
|
|
What is the most common risk factor for surface derived ovarian CA?
|
nulliparity because of increase of ovulatory cycles
|
|
What is the most common risk factor for Malignant lymphoma thyroid?
|
Hashimoto's Thyroiditis
|
|
What is the most common risk factor for papillary CA of thyroid?
|
Ionization Radiation
|
|
What is the most common risk factor for medullary CA thyroid?
|
MEN IIa/IIb
|
|
What is the most common risk factor for Primary CNS lymphoma?
|
EBV in AIDS pat.
|
|
What activates the alternative complement pathway?
|
Microbe surface molecules (especially endotoxin)
|
|
What drug prevents mast cell degranulation?
|
Cromolyn sodium
|
|
What is the primary function of a basophil?
|
Mediates allergic reactions
|
|
What activates the classic complement pathway?
|
IgG and IgM GM makes classic cars
|
|
What releases Interferon gamma
|
Th1 cells (emphasized) and NK cells
|
|
What are released from the process of degranulation in mast cells?
|
Release of histamine, heparin, and eosinophil chemotactic factors
|
|
Innate immunity vs adaptive immunity: How are receptors that recognize pathogens encoded?
|
Innate: Germline encoded Adaptive: Undergo VDJ recombination during development
|
|
What is the primary phagocytic cell in acute inflammation?
|
Neutrophil
|
|
What percentage of T cells which enter thymus survive?
|
2%
|
|
Name 2 substances produced by an eosinophil.
|
histamine and arylsulfatase
|
|
What cell is the major mediator of the allergic response?
|
Basophil
|
|
What are the two types of helper T cells and where do they differentiate?
|
In the lymph node, helper T cells differentiate into Th1 cells, and Th2 cells.
|
|
What are 4 types of cells into which T cells differentiate?
|
Cytotoxic T cells (MHC I, CD8) , Helper T cells (MHCII, CD4) , Suppressor T cells , Delayed hypersensitivity T cells
|
|
What releases Tumor Necrosis Factor alpha
|
Macrophages (emphasized) and Th1 cells
|
|
What is the response of an eosiniphil to antigen antibody complexes?
|
high degree of phagocytosis
|
|
What substance in eosinophilic granules is mainly responsible for defense against helminths and protozoan?
|
Major Basic Protein
|
|
Where do positive and negative selection of T-cells occur in the thymus?
|
At the corticomedullary junction
|
|
MHC I and II: Where in the cell is antigen loaded onto the MHC?
|
I: RER (mostly intracellular peptides) II: Acidified endosome
|
|
Into what cell type does a monocyte differentiate in tissues?
|
macrophages
|
|
What releases Interleukin 2?
|
Th Cells
|
|
What is the function of IgA proteases?
|
Function: Allow some organisms to colonize mucosal surfaces
|
|
What is the function and chemical composition of bacterial structure: Capsule
|
Function: Protects against phagocytosis Chemical composition: Polysaccharide (except Bacillus anthracis which contains D-glutamate)
|
|
What is the function and chemical composition of bacterial structure: Cell Wall/Cell Membrane
|
Gram positives only Function: Major surface antigen Chemical composition: Teichoic acid, which induces TNF and IL-1
|
|
What does the capsule of Bacillus anthracis consist of?
|
D-glutamate
|
|
What is the mechanism of superantigens?
|
1. Bind directly to MHC II and T cell receptor 2. Large numbers of T cells are activated. 3. Stimulates release of IFN-gamma and IL-2
|
|
Which molecule, unique to the bacterial cell wall, provides rigid support and resistance against osmotic pressure?
|
Peptidoglycan
|
|
Which cell membrane structure is unique to gram-positive organisms?
|
Teichoic acid
|
|
What is the function and chemical composition of bacterial structure: Peptidoglycan
|
Function: Rigid support and Protects against osmotic pressure Chemical composition: Sugar backbone with cross-linked peptide side chains
|
|
List of bugs that release superantigens
|
1. Staphylococcus aureus 2. Streptococcus pyogenes
|
|
What is the function and chemical composition of bacterial structure: Glycocalyx
|
Function: Mediates adherence to surfaces, especially foreign surfaces (eg indwelling catheters) Chemical composition: Polysaccharide
|
|
Which bacteria have IgA proteases?
|
1. Streptococcus pneumoniae 2. Neisseria meningitidis 3. Neisseria gonorrheae 4. Hemophilus influenzae
|
|
Why does the following bug not gram stain well?: Treponema
|
Too thin to be visualized
|
|
Why does the following bug not gram stain well?: Rickettsia
|
Intracellular parasite
|
|
Why does the following bug not gram stain well?: Mycobacteria
|
high-lipid-content cell wall
|
|
Why does the following bug not gram stain well?: Mycoplasma
|
No cell wall
|
|
Why does the following bug not gram stain well?: Legionella pneumophila
|
Primarily intracellular
|
|
Why does the following bug not gram stain well?: Chlamydia
|
Intracellular parasite which lacks muramic acid in cell wall
|
|
How is the following bug visualized?: Treponema
|
1. Darkfield microscopy 2. Fluorescent antibody staining 3. silver stain
|
|
What to know about exotoxins released by Shigella
|
Shiga toxin (also produced by E.coli 0157:H7). Cleaves host cell rRNA. Also enhances cytokine release causing hemolytic uremic syndrome.
|
|
Endotoxin: What is it and where is it found?
|
Lipopolysaccharide found in the outer membrane of gram-negative bacteria. Heat stable.
|
|
Endotoxin: What does it activate and what do they release?
|
1. Macrophages (IL-1, TNF, Nitric oxide) 2. Alternative complement pathway (C3a, C5a) 3. Hageman factor (Coagulation cascade)
|
|
What mediators are released when endotoxin activates macrophages, and what do they do?
|
1. IL-1: Fever 2. TNF: Fever and Hemorrhagic tissue necrosis 3. Nitric Oxide: Hypotension (shock)
|
|
What mediators are released when endotoxin activates the alternative complement cascade, and what do they do?
|
1. C3a: Hypotension and edema 2. C5a: Neutrophil chemotaxis
|
|
What mediators are released when endotoxin activates Hageman factor, and what do they do?
|
Coagulation cascade: Disseminated intravascular coagulopathy
|
|
What are the pigment producing bacteria and what pigments do they produce?
|
Staphylococcus aureus: Yellow pigment; Pseudomonas aeruginosa: blue-green pigment; Serratia marcescens: red pigment
|
|
Special culture requirements for: Hemophilus influenzae
|
Chocolate agar with factors V (NAD) and X (hematin)
|
|
Special culture requirements for: Neisseria gonorrhoeae
|
Thayer-Martin media
|
|
Special culture requirements for: Bordetella pertussis
|
Bordet-Gengou (potato) agar
|
|
Special culture requirements for: M. tuberculosis
|
Lowenstein-Jensen agar
|
|
Special culture requirements for: Lactose-fermenting enteric bacteria
|
Pink colonies on MacConkey's agar
|
|
Special culture requirements for: Legionella
|
Charcoal yeast extract agar buffered with increased iron and cysteine
|
|
Special culture requirements for: Fungi
|
Sabouraud's agar
|
|
What microbes can be stained with: Giemsa's
|
1. Borrelia 2. Plasmodium 3. Trypanosomes 4. Chlamydia
|
|
What microbes can be stained with: periodic acid-Schiff (PAS)
|
Glycogen and mucopolysaccharides. Used to diagnose Whipple's disease
|
|
What microbes can be stained with: Ziehl-Neelsen
|
Acid-fast bacteria.
|
|
What microbes can be stained with: Silver stain
|
1. Fungi 2. PCP (Pneumocystis Pneumonia) 3. Legionella 4. Treponema
|
|
Name 4 lysogenic toxins.
|
BCDE 1. Botulinum 2. Cholera 3. Diphtheria 4. Erythrogenic toxin of Streptococcus Pyogenes
|
|
List four obligate aerobes.
|
Nocardia, Pseudomonas aeruginosa, Mycobacterium tuberculosis, Bacillus
|
|
List 3 obligate anaerobes
|
Clostridium, Bacteroides, and Actinomyces
|
|
What enzymes do obligate anaerobes lack?
|
Catalase (aka glutathione peroxidase) AND/OR Superoxide dismutase (converts O2-radical[ie superoxide] to H2O2)
|
|
What do anaerobes produce in tissue?
|
CO2 and H2 gases
|
|
List the obligate intracellular bacteria.
|
Rickettsia and Chlamydia.
|
|
What is the defining characteristic of obligate intracellular bacteria.
|
Can't make their own ATP.
|
|
List the facultative intracellular bacteria.
|
Salmonella, Neisseria, Brucella, Mycobacterium, Listeria, Francisella, Legionella, Yersinia
|
|
List four major examples of encapsulated bacteria
|
1. Streptococcus pneumoniae 2. Hemophilus influenzae (especially B serotype) 3. Neisseria meningitidis 4. Klebsiella pneumoniae
|
|
In which vaccines does the capsule serve as an antigen?
|
Pneumovax, H influenzae B, Meningococcal vaccines
|
|
What does conjugation with protein do to vaccines that have a capsular antigen?
|
Increases the immunogenicity and T-cell dependent responce.
|
|
Which bacteria form spores?
|
Gram positive soil bugs (eg Bacillus anthracis, Clostridium perfringens, Clostridium tetani)
|
|
Which bacteria are beta-hemolytic?
|
Rods: Listeria monocytogenes Cocci:If catalase positive and coagulase positive: Staphylococcus Aureus, If catalase negative, Streptococcus.
|
|
What are the important points about Listeria monocytogenes?
|
1. Tumbling motility 2. Meningitis in newborns 3. Unpasteurized milk 4. endotoxin
|
|
Which antibody enhances host defenses against Streptococcus Pyogenes?
|
Antibody to M protein
|
|
Antibody to M protein enhances host defenses against what?
|
Streptococcus Pyogenes
|
|
How can one detect recent S. Pyogenes infection?
|
ASO titer
|
|
What drug resistances do the enterococci show?
|
1. Penicillin G 2. Ampicillin 3. Vancomycin
|
|
How are clostridia characterized?
|
1. Gram positive rods 2. Spore forming 3. Obligate anaerobes
|
|
Treatment for C. difficile infection
|
Metronidazole
|
|
Lab diagnosis basis for Cornyebacterium diphtheriae
|
Gram positive rods with metachromatic granules, grown on tellurite agar (aka Loffler's coagulated serum medium)
|
|
What organism: Development of flulike symptoms followed by fever, pulmonary hemorrhage and shock.
|
Inhalation anthrax: Bacillus anthracis
|
|
What organism: Oral or facial abscesses with yellow granules in sinus tracts
|
Actinomyces israelii
|
|
How is Nocardia asteroides characterized?
|
Gram-positive (weakly acid fast) rods forming long branching filaments resembling fungi (Actinomyces also has this description)
|
|
What disease state does Nocardia asteroides cause?
|
Pulmonary infection in immunocompromised patients
|
|
What bacteria genus can live in neutrophils?
|
Neisseria
|
|
What disease states does Gonococcus cause?
|
1. Gonorrhea 2. septic arthritis 3. neonatal conjunctivitis 4. PID
|
|
What disease states does Meningococcus cause?
|
1. Meningococcemia 2. Meningitis 3. Waterhouse-Friderichsen syndrome
|
|
What disease states does Haemophilus Influenzae cause?
|
1. Epiglottitis 2. Meningitis 3. Otitis media 4. Pneumonia
|
|
How is Haemophilus Influenzae characterized?
|
Small gram-negative coccoid rod.
|
|
Treatment for Haemophilus Influenzae meningitis
|
Ceftriaxone
|
|
What disease states does Klebsiella cause?
|
1. Pneumonia in alcoholics and diabetics (In the name: Klebsiella pneumoniae) 2. Nosocomial UTIs (large mucoid capsule and viscous colonies)
|
|
Orange sputum: What bugs?
|
1. Pneumococcus 2. Klebsiella (or described as ""red currant jelly sputum"")
|
|
Salmonella vs. Shigella: Lactose fermenter?
|
Neither
|
|
Salmonella vs. Shigella: Motile
|
Both (Though, the evidence that shigella is motile is recent.) Can invade and disseminate hematogenously.
|
|
Salmonella vs. Shigella: Animal reservoir
|
Salmonella: Yes Shigella: No
|
|
Shigella transmission
|
4 Fs:1. Food 2. Fingers 3. Feces 4. Flies
|
|
What type of inflammatory response is seen in Salmonellosis?
|
Monocytes
|
|
Transmission of Yersinia enterocolitica
|
1. Pet feces (eg puppies) 2. Contaminated milk or pork
|
|
Yersinia enterocolitica infection: Clinical presentation
|
1. Outbreaks are common in day-care centers 2. Can mimic Crohn's or appendicitis
|
|
What bug causes contamination of this food: Seafood
|
Vibrio: 1. parahaemolyticus 2. vulnificus
|
|
What bug causes contamination of this food: Reheated meat
|
Clostridium perfringens
|
|
Bloody or watery diarrhea: Vibrio parahaemolyticus
|
Either bloody or watery
|
|
Bloody or watery diarrhea: Campylobacter
|
Bloody
|
|
Bloody or watery diarrhea: Salmonella
|
Bloody
|
|
Bloody or watery diarrhea: Yersinia enterocolitica
|
Bloody
|
|
Bloody or watery diarrhea: C. difficile
|
Bloody
|
|
Bloody or watery diarrhea: Entamoeba histolytica
|
Bloody
|
|
Bloody or watery diarrhea: Enterotoxigenic E. coli
|
Watery
|
|
Bloody or watery diarrhea: C. perfringens
|
Watery
|
|
Bloody or watery diarrhea: Protozoa
|
Watery
|
|
Bloody or watery diarrhea: Viruses
|
Watery
|
|
Diagnosis: Bloody diarrhea with oxidase-positive comma or S-shaped organisms grown at 42 degrees celsius
|
Campylobacter
|
|
Diagnosis: Bloody diarrhea with motile, lactose negative gram negative bugs
|
Salmonella or Shigella
|
|
Diagnosis: Bloody diarrhea with schistocytes and azotemia
|
Enterohemorrhagic E coli (eg O157:H7) Caused by shiga-like toxin
|
|
Diagnosis: Bloody diarrhea with hemolytic uremic syndrome
|
Enterohemorrhagic E coli (eg O157:H7) Caused by shiga-like toxin
|
|
Diagnosis: Bloody diarrhea with pathologic section revealing bacteria invading colonic mucosa
|
Enteroinvasive E. coli
|
|
Diagnosis: Bloody diarrhea with symptoms of appendicitis
|
Yersinia enterocolitica
|
|
Diagnosis: Bloody diarrhea in a day care center
|
Yersinia enterocolitica
|
|
Diagnosis: Watery diarrhea in someone who just visited Mexico
|
Enterotoxigenic E coli (no preformed toxin)
|
|
Diagnosis: Watery diarrhea in an immunocompromised patient
|
Protozoa (eg Giardia or Cryptosporidium)
|
|
Diagnosis: Watery diarrhea
|
Think viruses first. Rotavirus Adenovirus Norwalk virus
|
|
Difference between mechanisms of cholera and pertussis toxins
|
Cholera: Permanently activates Gs (turns the "on" on) Pertussis: Permanently disables GI (turns the "off"" ff)
|
|
What is edema factor?
|
A toxin in the Bacillus Anthracis exotoxin complex that functions as adenylyl cyclase
|
|
Describe Legionnaires' disease
|
Very high fever with severe pneumonia
|
|
Diagnosis: Pneumonia in a smoker >50 years of age. Gram stain of pus shows many neutrophils with few microbes.
|
Legionella
|
|
Which fungal infections are transmitted by inhalation of asexual spores?
|
1. Coccidioidomycosis 2. Histoplasmosis
|
|
What are conidia?
|
Asexual fungal spores
|
|
Histologic appearance of Candida Albicans
|
Budding yeast with pseudohyphae in culture at 20 degrees celsius Germ tube formation at 37 degrees celsius
|
|
What fungus is this area known for: Southern Ohio
|
Histoplasmosis
|
|
What fungus is this area known for: Southern Illinois
|
Histoplasmosis
|
|
What fungus is this area known for: Missouri
|
Histoplasmosis
|
|
What fungus is this area known for: Kentucky
|
Histoplasmosis
|
|
What fungus is this area known for: Tennessee
|
Histoplasmosis
|
|
What fungus is this area known for: Arkansas
|
Histoplasmosis
|
|
What fungus is this area known for: Mississippi river valley
|
Histoplasmosis (also Blastomycosis)
|
|
What fungus is this area known for: Ohio river valley
|
Histoplasmosis (also Blastomycosis)
|
|
What fungus is this area known for: Wisconsin
|
Blastomycosis
|
|
What fungus is this area known for: Minnesota
|
Blastomycosis
|
|
What do bird and bat droppings carry?
|
Histoplasmosis
|
|
What is cultured on Sabouraud's agar?
|
Fungi (specifically dimorphic fungi)
|
|
What disease state does Malassezia furfur cause?
|
Tinea versicolor: Hypopigmented skin lesions which occur in hot humid weather.
|
|
Treatment for Tinea versicolor
|
Topical miconazole or selenium sulfide (Selsun)
|
|
What disease state does Cladosporium werneckii cause?
|
Tinea nigra: Infection of keratinized layer of skin. Appears as brownish spot.
|
|
What causes Tinea versicolor?
|
Malassezia furfur
|
|
What causes Tinea nigra?
|
Cladosporium werneckii
|
|
Treatment for Tinea nigra
|
topical salicylic acid
|
|
What are the common dermatophytes and what do they cause?
|
Microsporum, Trichophyton, and Epidermophyton cause all the tineas except for versicolor and nigra
|
|
What causes Tinea unguium (onychomycosis)?
|
AKA Tinea onychomycosis. Dermatophytes (such as Microsporum, Trichophyton, and Epidermophyton)
|
|
Treatment for dermatophyte infection
|
1. Topical imidazoles 2. Oral griseofulvin (Tinea capitus and tinea unguium)
|
|
What causes a fungus ball?
|
Aspergillus
|
|
What disease states does Aspergillus cause?
|
1. Allergic bronchopulmonary aspergillosis 2. Lung cavity aspergilloma 3. Invasive aspergillosis
|
|
What disease states does cryptococcus neoformans cause?
|
1. Cryptococcal meningitis 2. Cryptococcosis
|
|
How is cryptococcus neoformans stained?
|
1. India ink 2. Latex agglutination test for polysaccharide capsular antigen
|
|
Where is cryptococcus neoformans found?
|
Soil and pigeon droppings.
|
|
What is the histologic appearance of Mucor (Rhizopus) ?
|
Just like Rhizopus Mold with irregular, broad, empty looking, nonseptate hyphae branching at wide angles (over 90 degrees)
|
|
Which patients are likely to have Mucor/Rhizopus?
|
1. Ketoacidotic diabetics 2. Leukemics
|
|
Where in the body does Mucor/Rhizopus proliferate?
|
1. Walls of blood vessels, causing infarction of distal tissue 2. Rhinocerebral frontal lobe abscesses
|
|
How is pneumocystis diagnosed?
|
Lung biopsy or lavage. Methenamine silver stain of lung tissue.
|
|
Treatment for pneumocystis
|
Combination of TMP-SMX, Pentamidine, and Dapsone.
|
|
Treatment for sporotrichosis
|
Itraconazole or potassium iodide
|
|
What disease states does Entamoeba histolytica cause?
|
1. Amebiasis 2. Bloody diarrhea (dysentery) 3. liver abscess 4. RUQ pain
|
|
What disease states does Giardia lamblia cause?
|
1. Giardiasis 2. Bloating 3. Flatulence 4. Foul-smelling diarrhea
|
|
What diseases are found in campers and hikers?
|
Yersinia pestis and Giardia lamblia
|
|
What disease states does Cryptosporidium cause?
|
Diarrhea 1. AIDS: Severe 2. Non-HIV: Mild watery
|
|
What disease states does Toxoplasma cause?
|
1. HIV: Brain abscess 2. Birth defects (ring-enhancing brain lesions)
|
|
What disease states does Leishmania donovani cause?
|
Visceral leishmaniasis (kala-azar or black fever): fever, weight loss, anaemia and substantial swelling of the liver and spleen
|
|
What disease states does Naegleria cause?
|
Rapidly fatal meningoencephalitis
|
|
What disease states does Babesia cause?
|
Babesiosis: Fever and anemia
|
|
Which protozoa are transmitted by cysts?
|
1. Entamoeba histolytica 2. Giardia lamblia 3. Cryptosporidium 4. Toxoplasma All water cysts except Toxo (cysts in meat or cat feces)
|
|
Which protozoa are transmitted by swimming in freshwater lakes?
|
Naeglaria (via cribriform plate)
|
|
Which protozoa are transmitted by reduviid bug?
|
Trypanosoma cruzi (the enses are transmitted by the tsetses, cruzii by reduviid))
|
|
Which protozoa are transmitted by tsetse fly?
|
Trypanosoma gambiense and rhodesiense (the enses are transmitted by the tsetses, cruzii by reduviid))
|
|
Which protozoa are transmitted by sandfly?
|
Leishmania
|
|
Which protozoa are transmitted by ixodes tick?
|
Babesia
|
|
How do you diagnose: Entamoeba histolytica
|
1. Trophozoites or cysts in stool AND/OR 2. Serology
|
|
How do you diagnose: Cryptosporidium
|
Cysts on acid-fast stain
|
|
How do you diagnose: Toxoplasma
|
Serology, biopsy
|
|
How do you diagnose: Babesia
|
Blood smear, no RBC pigment, appears as ""maltese cross""
|
|
How do you diagnose: Leishmania
|
Macrophages containing amastigotes
|
|
How do you diagnose: Naegleria
|
Amebas in spinal fluid
|
|
Treatment for: Entameba histolytica
|
Metronidazole and iodoquinol
|
|
Treatment for: Giardia lamblia
|
Metronidazole
|
|
Treatment for: Cryptosporidium
|
None
|
|
Treatment for: Plasmodium
|
1. Choloroquine 2. additonal Primaquine ( to prevent relapse or liver damage) 3. sulfadoxine plus pyrimethamine 4. Mefloquine 5. Quinine
|
|
Treatment for: Trypanosoma cruzi
|
Nifurtimox
|
|
Treatment for: Trypanosoma gambiense and rhodesiense
|
If blood-borne, suramin. If CNS penetration, melarsoprol.
|
|
Treatment for: Leishmania
|
Sodium stibogluconate
|
|
Treatment for: Babesia
|
Qunine, clindamycin
|
|
Treatment for: Toxoplasma
|
Sulfadiazine plus pyrimethamine
|
|
Which worm: Undercooked pork
|
1. Taenia solium (tapeworm) 2. Trichinella spiralis (roundworm)
|
|
Which worm: Brain cysts
|
Taenia solium (tapeworm)
|
|
Which worm: Liver cysts
|
Echniococcus granulosus (tapeworm)
|
|
Important points about echinococcus granulosus
|
Tapeworm (Cestode) 1. Ingested eggs from dog feces 2. Liver cysts 3. Cysts release antigens and cause anaphylaxis
|
|
Taenia solium: Treatment
|
Praziquantel/niclosamide. Albendazole for cysticercosis
|
|
Echinococcus granulosus: Treatment
|
Albendazole
|
|
Characterization of Schistosoma
|
Fluke (Trematode) 1. Hosted by snails 2. Penetrate skin of humans
|
|
Schistosoma: Treatment
|
Praziquantel
|
|
Which worm: Portal hypertension
|
Schistosoma mansoni
|
|
Which worm: Hematuria
|
Schistosoma haematobium
|
|
Which worm: Bladder cancer
|
Schistosoma haematobium
|
|
Important points about Clonorchis sinensis
|
Fluke (trematode) 1. undercooked fish 2. Inflammation of biliary tract
|
|
Which worm: Undercooked fish
|
Clonorchis sinensis
|
|
Clonorchis sinensis: Treatment
|
Praziquantel
|
|
Which worm: B12 deficiency
|
Diphyllobothrium latum (tapeworm)
|
|
Which worm: Undercooked crab meat
|
Paragonimus westermani (fluke)
|
|
Important points about Pargonimus westermani
|
Trematode (fluke) 1. Undercooked crabmeat 2. Inflammation and secondary bacterial infection of the lung 3. Hemoptysis
|
|
Which worm: Hemoptysis
|
Paragonimus westermani (fluke)
|
|
Paragonimus westermani: Treatment
|
Praziquantel
|
|
Which worm: Microcytic anemia
|
Ancylostoma (aka hookworm) and Necator (both roundworms)
|
|
Important points about Ancylostoma duodenale
|
Nematode (roundworm) 1. Aka hookworm 2. Larvae penetrate skin of feet 3. Intestinal infection can cause anemia
|
|
Ancylostoma duodenale: Treatment
|
Mebendazole/pyrantel pamoate
|
|
Ascaris lumbricoides: Treatment
|
Mebendazole/pyrantel pamoate
|
|
Enterobius vermicularis: Treatment
|
Mebendazole/pyrantel pamoate
|
|
Important points about Strongyloides stercoralis
|
Nematode (roundworm) 1. Larvae in soil penetrate the skin 2. Intestinal infection
|
|
Strongyloides stercoralis: treatment
|
Ivermectin/thiabendazole
|
|
Important points about Trichinella spiralis
|
Roundworm (nematode) 1. Undercooked meat, usually pork 2. Inflammation of muscle 3. Periorbital edema
|
|
Trichinella spiralis: Treatment
|
Thiabendazole
|
|
Important points about Dracunculus medinensis
|
Nematode (roundworm) 1. In drinking water 2. Skin inflammation and ulceration
|
|
Dracunculus medinensis: Treatment
|
Niridazole
|
|
Important points about Loa loa
|
Nematode (roundworm) 1. Transmitted by deer fly 2. Causes swelling in skin 3. Can see worm crawling in conjunctiva
|
|
Loa loa: Treatment
|
Diethylcarbamazine
|
|
Important points about Onchocerca volvulus
|
Nematode (roundworm) 1. Transmitted by female blackflies 2. Causes river blindness
|
|
Onchocerca volvulus: Treatment
|
Ivermectin
|
|
Important points about Toxocara canis
|
Nematode (roundworm) 1. Food contaminated with eggs 2. Causes granulomas (if in retina, blindness) 3. Visceral larva migrans
|
|
Toxocara canis: Treatment
|
Diethylcarbamazine
|
|
Important points about Wuchereria bancrofti
|
Nematode (roundworm) 1. Female mosquito 2. Causes blockage of lymphatic vessels (elephantiasis)
|
|
Wuchereria bancrofti: Treatment
|
Diethylcarbamazine
|
|
Which DNA viruses have linear genomes?
|
All except papova virus and hepadna which are circular
|
|
Which DNA viruses have circular genomes?
|
papova virus and hepadna which are circular
|
|
Which DNA viruses have infectious naked nucleic acids?
|
Most dsDNA (except poxvirus and HBV)
|
|
Which DNA viruses have non-infectious naked nucleic acids?
|
poxvirus and HBV
|
|
Which enveloped viruses acquire their envelopes from the plasma membrane?
|
All except herpesviruses (nuclear membrane)
|
|
Which enveloped viruses acquire their envelopes from the nuclear membrane?
|
Only herpesviruses
|
|
Where do RNA viruses replicate?
|
Cytoplasm (except influenza and retroviruses)
|
|
Which DNA viruses are icosahedral?
|
All except pox (complex)
|
|
Which DNA viruses replicate in the nucleus?
|
All except pox (carries own DNA-dependent RNA polymerases)
|
|
Live/Killed and Egg-based/Recombinant: MMR vaccine
|
Live attenuated, egg-based
|
|
Live/Killed and Egg-based/Recombinant: Sabin polio vaccine
|
Live attenuated
|
|
Live/Killed and Egg-based/Recombinant: VZV vaccine
|
Live attenuated
|
|
Live/Killed and Egg-based/Recombinant: Yellow fever vaccine
|
Live attenuated, egg-based
|
|
Live/Killed and Egg-based/Recombinant: Smallpox vaccine
|
Live attenuated
|
|
Live/Killed and Egg-based/Recombinant: Adenovirus vaccine
|
Live attenuated
|
|
Live/Killed and Egg-based/Recombinant: Rabies vaccine
|
Killed
|
|
Live/Killed and Egg-based/Recombinant: Influenza vaccine
|
Killed, egg-based
|
|
Live/Killed and Egg-based/Recombinant: Salk polio vaccine
|
Killed
|
|
Live/Killed and Egg-based/Recombinant: HAV vaccine
|
Killed
|
|
What is this viral process: Exchange of genes between 2 chromosomes by crossing over within regions of significant base sequence homology
|
Viral recombination
|
|
Definition: Viral Reassortment
|
Viruses with segmented genomes exchange segments. Same as high frequency recombination. Cause of worldwide pandemics.
|
|
What is this viral process: Viruses with segmented genomes exchange segments.
|
Viral Reassortment Same as high frequency recombination. Cause of worldwide pandemics.
|
|
What is this viral process: When 1 of 2 viruses that infect the cell has a mutation that results in nonfunctional protein and the non-mutated virus makes a functional protein that serves both viruses.
|
Viral Complementation
|
|
What is this viral process: Genome of virus A can be coated with the surface proteins of virus B. Type B protein coat determines the infectivity of the phenotypically mixed virus.
|
Viral Phenotypic Mixing Progeny of type A however have type A coat from type A genes.
|
|
What does HBcAb measure?
|
Antibody to core antigen. Positive during window period (no HBsAg or HBsAb detected). IgM HBcAb is an indicator of recent disease.
|
|
What does HBeAg measure?
|
A second different antigenic determinant in the HBV core. Important indicator of transmissibility. (BEware!)
|
|
What does HBeAb measure?
|
Antibody to e antigen; indicates low transmissibility.
|
|
What is gag?
|
Gene that encodes for p24 capsid, the nucleocapsid in HIV
|
|
What is env?
|
Gene that encodes for gp41 and gp120 proteins, the envelope proteins in HIV.
|
|
What is p17?
|
Interior envelope protein in HIV
|
|
What is p24?
|
Nucleocapsid protein in HIV, coded for by gag gene.
|
|
What is gp41?
|
Envelope protein which traverses bilayer. If it is a mushroom stalk, then gp120 is the head. Both coded for by env.
|
|
What is gp120?
|
Envelope protein that serves as mushroom cap to gp41 stalk. Both coded for by env.
|
|
What is pol?
|
Gene which codes for HIV reverse transcriptase
|
|
Common causes of osteomyelitis in sexually active people.
|
Neisseria gonorrhoeae (rare), septic arthritis more common
|
|
Common causes of osteomyelitis in diabetics.
|
Pseudomonas aeruginosa
|
|
Common causes of osteomyelitis in drug addicts.
|
Pseudomonas aeruginosa
|
|
Common causes of osteomyelitis in people with prosthetic replacement
|
Staphylococcus aureus and Staphylococcus epidermidis
|
|
Common causes of urinary tract infections in ambulatory people
|
Mostly ascending infections 1. E. coli (50-80%) 2. Staphylococcus saprophyticus (10-30%) in young amubulatory women 3. Klebsiella (8-10%)
|
|
Common causes of urinary tract infections in the hospital
|
Mostly ascending infections 1. E. coli 2. Proteus 3. Klebsiella 4. Serratia 5. Pseudomonas
|
|
Risk factor for nosocomial CMV infection.
|
Newborn nursery
|
|
Risk factor for nosocomial RSV infection.
|
Newborn nursery
|
|
Risk factor for nosocomial E. coli infection.
|
Urinary catheterization
|
|
Risk factor for nosocomial Proteus mirablis infection.
|
Urinary catheterization
|
|
Risk factor for nosocomial Pseudomonas aeruginosa infection.
|
Respiratory therapy equipment
|
|
Risk factor for nosocomial Candida albicans infection.
|
Hyperalimentation
|
|
What bug: Empyema
|
Staphylococcus aureus (means pus in a natural body cavity, not an abscess)
|
|
What bug: Pediatric infection
|
Haemophilus influenzae
|
|
What bug: Sepsis in a newborn
|
Group B Strep
|
|
What bug: Meningitis in a newborn
|
Group B Strep
|
|
What organism is associated w/ HLA-B27 spondyloarthropathy and uremic Sx?
|
Shigella
|
|
What is the MC contaminant of blood transfusions?
|
Yersenia enterocolitica
|
|
What are trophozoites phagocytosed RBCs?
|
Entameba histolytica (Ameba)
|
|
What organism causes chorioamnionitis?
|
Step. agalactiae
|
|
Most common: Ovarian tumor (malignant)
|
Serous cystadenocarcinoma
|
|
Most common: Mets to bone
|
Breast, lung, thyroid, testes, prostate, kidney
|
|
Most common: Mets to brain
|
Lung, breast, skin (melanoma), kidney (RCC), GI
|
|
Most common: Breast tumor (benign)
|
Fibroadenoma
|
|
Most common: Brain tumor (kids)
|
Medulloblastoma (cerebellum)
|
|
Most common: Preventable cancer
|
Lung cancer
|
|
Most common: Breast mass
|
Fibrocystic change (in postmenopausal wormen, carcinoma in the most common)
|
|
Most common: Tumor of the adrenal medulla (kids)
|
Neuroblastoma (malignant)
|
|
Most common: Bacteria found in GI tract
|
Bacteroides (2nd most common is E. coli)
|
|
Most common: Bacteremia/pneumonia (IVDA)
|
S. aureus
|
|
Most common: Primary hyperparathyroidism
|
Adenomas (followed by hyperplasia, then carcinoma)
|
|
Most common: Breast cancer
|
Infiltrating ductal carcinoma (in the US, 1 in 9 women will develop breast cancer)
|
|
Most common: Site of metastasis (2nd most common)
|
Liver
|
|
Most common: Gynecologic malignancy
|
Endometrial carcinoma
|
|
Most common: Brain tumor-supratentorial (kids)
|
Craniopharyngioma
|
|
Most common: Skin cancer
|
Basal cell carcinoma
|
|
Most common: Ovarian tumor (benign)
|
Serous cystadenoma
|
|
Most common: Tumor in women
|
Leiomyoma (estrogen dependent)
|
|
Most common: Vasculitis
|
Temporal arteritis (risk of ipsilateral blindness due to thrombosis of ophthalmic artery)
|
|
Most common: Viral encephalitis
|
HSV
|
|
Most common: Bug in debilitated, hospitalized pneumonia patient
|
Klebsiella
|
|
Most common: Site of metastasis
|
Regional lymph nodes
|
|
Most common: Nephrotic syndrome
|
Membranous glomerulonephritis
|
|
Most common: Type of Hodgkin's
|
Follicular, small cleaved
|
|
Most common: Organ sending mets
|
Lung>breast, stomach
|
|
Most common: Organ receiving mets
|
Adrenal glands (due to rich blood supply)
|
|
Most common: Neoplasm (kids)
|
ALL (2nd most common is cerebellar medulloblastoma)
|
|
Most common: Tumor of infancy
|
Hemangioma
|
|
Most Frequent Cause of: Addison's
|
Autoimmune (infection is the 2nd most common cause)
|
|
Most Frequent Cause of: Bacterial meningitis (adults)
|
Streptococcus pneumoniae
|
|
Most Frequent Cause of: UTI (young women)
|
E. coli and Staphylococcus saprophyticus
|
|
Most Frequent Cause of: Bacterial meningitis (kids)
|
S. pneumoniae or Neisseria meningitidis
|
|
Most Frequent Cause of: Hypopituitarism
|
Adenoma
|
|
Most Frequent Cause of: Right-sided heart failure
|
Left-sided heart failure
|
|
Most Frequent Cause of: PID
|
Neisseria gonorrhoeae (monoarticular arthritis)
|
|
Most Frequent Cause of: Bacterial meningitis (elderly)
|
S. pneumoniae
|
|
Most Frequent Cause of: SIADH
|
Small cell carcinoma of the lung
|
|
Are D1 neurons in the basal ganglia inhibitory or excitatory?
|
Excitatory
|
|
What part of the hypothalamus (ant./post.) controls autonomic regulation?
|
anterior hypothalamus
|
|
How can a Nissl stain be used to differentiate microglia from oligodendroglia?
|
Microglia are not discernible in a Nissl stain while oligodendroglia appear as small dark nuclei with dark chromatin
|
|
What part of the hypothalamus (ant./post.) controls cooling when hot?
|
anterior hypothalamus
|
|
What nucleus of the hypothalamus controls sexual emotions?
|
septate nucleus
|
|
What midbrain structure is important in mitigating voluntary movements and making postural adjustments?
|
Basal Ganglia
|
|
Are D2 neurons in the basal ganglia inhibitory or excitatory?
|
Inhibitory
|
|
What is the 'gap' between the myelination segment of 2 Schwann cells called?
|
Node of Ranvier
|
|
What nucleus of the hypothalamus controls thirst and water balance?
|
supraoptic nucleus
|
|
What nucleus of the hypothalamus controls hunger?
|
lateral nucleus
|
|
What is the response of microglia to tissue damage?
|
transformation into large ameboid phagocytic cells
|
|
What nucleus of the hypothalamus controls circadian rhythms?
|
suprachiasmatic nucleus
|
|
What nucleus of the hypothalamus controls satiety?
|
ventromedial nucleus
|
|
What part of the hypothalamus (ant./post.) controls heat conservation when cold?
|
posterior hypothalamus
|
|
What is the equation to calculate loading dose?
|
(Cp)(Vd)/F (note: Cp = target plasma concentration, and F = bioavailability)
|
|
These specific drugs disrupt fungal cell membranes
|
amphotericin B, nystatin, fluconazole/azoles (FAN the fungal cell membranes)
|
|
Which drug blocks mRNA synthesis?
|
Rifampin
|
|
When would you use aminoglycosides?
|
Against severe gram-negative rod infections.
|
|
What is the equation to calculate the maintenance dose?
|
(Cp)(CL)/F (note: Cp = target plasma concentration, and F = bioavailability)
|
|
These drugs block nucleotide synthesis by interfering with the folate pathway
|
Sulfonamides (e.g. Bactrim), trimethoprim
|
|
These drugs disrupt the bacterial/fungal cell membranes
|
Polymyxins
|
|
What should you watch out for when giving penicillin?
|
Hypersensitivity reaction (urticaria,severe pruritus) and hemolytic anemia
|
|
Bacitracin, vancomycin and cycloserine block the synthesis of this molecule, preventing cell wall synthesis.
|
Peptidoglycans
|
|
What can 3rd generation cephalosporin drugs do that 1st and 2nd generation can't?
|
Cross the blood brain barrier.
|
|
What is the mechanism of action of Pentamidine?
|
Unknown
|
|
Which drugs are the bacteriacidal antibiotics?
|
Penicillin, cephalosporin, vancomycin, aminoglycosides, fluoroquinolones, metronidazole
|
|
What is the antidote for (TCA) Tricyclic Antidepressants toxicity/overdose
|
NaHCO3
|
|
This antimetabolite derivative of 6-mercaptopurine interferes with the metabolism and synthesis of nucleic acid.
|
azathioprine
|
|
Azaothioprine is used to in what setting?
|
Kidney transplants, autoimmune disorders (glomerulonephritis, hemolytic anemia)
|
|
Recombinant Cytokine- Aldesleukin (interleukin-2) is used for?
|
Renal cell carcinoma, metastatic melanoma
|
|
Recombinant Cytokine- alpha interferon is used for?
|
Hep B/C, Kaposi's sarcoma, leukemia, malgnant melanoma
|
|
Recombinant Cytokine- oprelvekin (interleukin-11) is used for?
|
Thrombocytopenia
|
|
Recombinant Cytokine- sargamostim is used for?
|
Recovery of Bone Marrow (it is a granulocyte-macrophage colony stimulating factor)
|
|
Weak acids, such as phenobarbitol, methotreaxate, aspirin, alkanize urine with ____ to increase clearance
|
bicarbonate
|
|
Weak bases, such as amphetamines, acidify urine with NH4Cl to ____ clearance
|
increase
|
|
-ane
|
inhalational general anesthetic. Halothane
|
|
-azepam
|
benzodiazepine. Diazepam
|
|
-azole
|
antifungal. Ketoconazole
|
|
-oxin
|
cardiac glycoside (inotropic agent). Digoxin
|
|
-terol
|
beta-2 agonist. Albuterol
|
|
-triptyline
|
tricyclic antidepressant. Amitriptyline
|
|
-tropin
|
pituitary hormone. Somatotropin
|
|
What is the complication of Sleep Apnea?
|
Pulmonary Hypertension- vasoconstrictive effects of chronic hypoxemia and respiratory acidosis called COR-PULOMONALE
|
|
What three compounds increase surfactant?
|
Thyroxin, Prolactin, and Glucocorticoid
|
|
What is the importance of the lecithin:sphingomyelin ratio?
|
A ratio greater than 2.0 in fetal lung is indicative of fetal lung maturity
|
|
What is found in the physical exploration of Atelectasis?
|
Dullness to percussion and Absent tactile fremitus
|
|
What is the last segment of lung tissue in which ciliated cells are found?
|
Respiratory Bronchioles
|
|
Where is surfactant stored?
|
Lamellar bodies
|
|
What process occurs when type I pneumocytes are damaged?
|
Type II pneumocytes develop into Type I
|
|
What is the last segment of lung tissue in which goblet cells are found?
|
Terminal Broncioles (remember ciliated cells sweep away mucous produced by goblet cells and therefore run deeper)
|
|
What is the diagnosis of a child w/ Nasal Polyps? Test for?
|
Sweat Test, Cystic Fibrosis (CF) until proven otherwise
|
|
Where do infarctions of the lung usually occur?
|
Lower lobes
|
|
What is another name for pulmonary surfactant?
|
DPPC (dipalmitoylphosphatidylcholine)
|
|
Why does Mucor species prevail in sinusitis of Diabetic patients?
|
Ketoacidosis causes proliferation
|
|
Newborn that turns cyanotic when breast feeding; cries and turns back to pink. Diagnosis?
|
Choanal Atresia
|
|
What is the pathogenesis of Respiratory Distress Syndrome in Newborns?
|
Atelectasis due to loss of surfactant
|
|
When does synthesis of surfactant begin?
|
28th week and reaches production peak at 35 weeks
|
|
How do you calculate the A-a gradient?
|
Alveolar PO2= 21%O2(Atm. P-47)-pCO2/0.8; A= (.21)(713)- 40/0.8); Usually A=100; A-a; a=95; normal A-a=5-30
|
|
When is A-a gradient indicative of pulmonary pathology?
|
when A-a grad = >30
|
|
Patient w/ fibromyalgia and develops asthma, what is the cause of this?
|
Aspirin induced asthma; block PG but still produce Leukotriene build up; LT C-D-E4 buildup (potent bronchoconstrictors)
|
|
Causes of Hypoxemia w/ normal A-a gradient?
|
-barbiturates OD-epiglottitis (Upper Airway Obstr.)-Amyotrophics Lat. Sclerosis (ALS)
|
|
What is the Diagnosis if pregnant woman presents w/ pre-eclampsia in first trimester?
|
hydatidiform mole
|
|
What two substances are increased in pre-eclampsia?
|
Angiotensin II; TXA2
|
|
What substances are decrease in pre-eclampsia?
|
PGE1 and NO
|
|
What is the macula densa?
|
Sodium sensor in part of the distal convoluted tubule in the juxtaglomerular apparatus of the kidney
|
|
What are JG cells?
|
Modified smooth muscle of afferent arteriole in the juxtaglomerular apparatus of the kidney
|
|
How is the glomerular basement membrane formed?
|
From the fusion of endothelial and podocyte basement membranes.
|
|
What is the function of the JG cells?
|
Secrete renin and erythropoietin
|
|
When do the JG cells secrete renin?
|
In response to decreased renal BP, decreased sodium delivery to distal tubule, and increased sympathetic tone
|
|
What is the glomerular basement membrane coated with? (provides negative charge to filter).
|
Negatively charged heparan sulfate.
|
|
Where is type II collagen found? (3)
|
1. cartilage (including hyaline) 2. vitreous body 3. nucleus pulposus.
|
|
What is the most abundant protein in the human body?
|
Collagen.
|
|
Where is type I collagen found?(7)
|
1. bone 2. tendon 3. skin 4. dentin 5. fascia 6. cornea 7. late wound repair
|
|
Define Pacinian corpuscles.
|
Large, encapsulated sensory receptors found in deeper layers of skin at ligaments, joint capsules, serous membranes, mesenteries.
|
|
Describe the appearance and status of primary vs. secondary follicles.
|
Primary follicles are dense and dormant. Secondary follicles have pale central germinal centers and are active.
|
|
Where is type III collagen found? (5)
|
1. skin 2.blood vessels 3.uterus 4.fetal tissue 5.granulation tissue
|
|
What is the function of Meissner's corpuscles?
|
Meissner's corpuscles are involved in light discriminatory touch of glabrous skin.
|
|
What is another name for type III collagen?
|
reticulin
|
|
What is the function of Pacinian corpuscles?
|
Pacinian corpuscles are involved in pressure, coarse touch, vibration, and tension.
|
|
Where is type X collagen found? (1)
|
epiphyseal plate
|
|
Define Meissner's corpuscles.
|
Small, encapsulated sensory receptors found in dermis of palm, soles and digits of skin.
|
|
Name the layers of epidermis from surface to base.
|
stratum Corneum, stratum Lucidum, stratum Granulosum, stratum Spinosum, stratum Basalis.
|
|
What is the most common type of collagen?
|
Collagen Type I - 90%
|
|
Where is type IV collagen found? (1)
|
basement membrane or basal lamina
|
|
What is more fatal, exotoxin or endotoxin?
|
exotoxin
|
|
What induces high-titer antibodies and is used in vaccines, exotoxin or endotoxin?
|
exotoxin
|
|
Binds directly to MHC-II and T-cell receptor activating T cells to release IFN-gamma and IL-2
|
Superantigens; TSST-1
|
|
Responsible for toxic shock syndrome?
|
TSST-1 released by Staph. aureus; Strep. pyogenes can also cause toxic shock-like symptoms
|
|
Most common cause of meningitis, otitis media (children), pneumonia, and sinusitis
|
Streptococcus pneumonia; "MOPS"
|
|
ADP ribosylating toxin stimulates adenylate cyclase to cause whooping cough?
|
Bordetella pertussis
|
|
This toxin cleaves host cell rRNA?
|
Shiga toxin produced by shigella (also produced by some strains of E. coli)
|
|
The toxin of this organism is a hemolysin?
|
streptolysin O of S. pyogenes(Beta hemolytic)
|
|
Endotoxin activates release of what factors from macrophages?
|
IL-1 (fever), TNF (fever, hemorrhagic tissue necrosis), NO (hypotension)
|
|
Endotoxin activates what factor to cause DIC?
|
Hageman factor
|
|
What are 3 common gram positive rods?
|
Clostridium, listeria, bacillus, corynebacterium
|
|
This coccoid rod requires chocolate agar with factor V and X for isolation.
|
Haemophilus influenzae
|
|
Gram negative "coccoid" rod which requires NAD and hematin for culture?
|
H. influenzae; NAD is factor V and hematin is factor X
|
|
Coccoid rod with an ADP ribosylating toxin?
|
Bordetella pertussis
|
|
Lactose non-fermenting rod, oxidase positive?
|
pseudomonas
|
|
This organism can cause bloody diarrhea, and mimic Crohn's or a "pseudoappendicitis".
|
Yersinia enterocolitica
|
|
Causes food poisoning in meats. (4 organisms)
|
S. aureus, C perfringens (reheated meat), E.coli, Salmonella
|
|
These 3 viruses cause watery diarrhea?
|
rotavirus, adenovirus, norwalk virus
|
|
The toxin of this organism is composed of a bacterial adenylate cyclase (edema factor) which increases cAMP.
|
Bacillus anthracis
|
|
What are common presentations of pseudomonas aeruginosa?
|
Burn and wound infections and Pneumonia (esp in CF), Sepsis (black lesions on skin), External otitis (swimmers ear), UTI, Diabetic osteomyelitis
|
|
This organism causes an undulant fever and is often acquired from dairy products.
|
Brucella
|
|
What is the treatment for G. vaginalis?
|
Metronidazole
|
|
What is the treatment for H. influenzae?
|
ceftriaxone (meningitis), rifampin (prophylaxis in close contacts)
|
|
Patient presents with fever, headache, and rash. Diagnosis?
|
Rickettsiae; classic triad of fever, headache and rash. Others my apply but if this is all you get, think Ricketts!
|
|
What is the Weil-Felix reaction?
|
antirickettsial antibodies, usually positive for rocky mountain spotted fever and typhus
|
|
What are the two forms of chlamydia?
|
Elementary body which is extracellular form that enters cell by endocytosis; Reticulate body which replicates in cell by fission
|
|
What are the 3 spirochetes?
|
Borrelia, leptospira, and treponema
|
|
BAX gene
|
activates apoptosis - activated by P53 gene if DNA damage is not repairable
|
|
BCL2 gene
|
inhibit apoptosis - prevent mitochondrial leakage of cytochrome c into the cytosol
|
|
ABL
|
nonreceptor tyrosine kinase activity - translocation associated with chronic myelogenous leukemia t(9:22) Philadelphia chromosome
|
|
HER2/ERBB2
|
synthesizes receptors; amplified in breast carcinoma; is a measure of aggressiveness of breast carcinoma
|
|
MYC
|
Involved in nuclear transcription; associated with the t(8;14) translocation in Burkitt's lymphoma
|
|
N-MYC
|
Involved in nuclear transcription; amplified in neuroblastoma
|
|
RAS
|
Point mutation. Involved in GTP signal transduction; a point mutation leads to leukemia and carcinomas
|
|
RET
|
synthesizes receptors; a point mutation leads to multiple endocrine neoplasia 2a/3b syndromes
|
|
SIS
|
synthesizes growth factors; overexpression of this gene leads to osteogenic sarcoma and astrocytoma
|
|
Translocation t(12;21)
|
favorable prognosis in pre-B-cell acute lymphoblastic leukemia
|
|
APC
|
Adenomatous polyposis coli; associated with familial polyposis (colorectal carcinoma); degrades catenin --> prevents nuclear transcription. 5q12
|
|
BRCA1/BRCA2
|
regulates DNA repair
|
|
TGF-B
|
Inhibits progression from G1 to S phase in the cell cycle. Associated with pancreatic and colorectal carcinomas.
|
|
VHL
|
regulates nuclear transcription; associated with Von Hippel Lindau Syndrome
|
|
WT1
|
regulates nuclear transcription; associated with Wilms' tumor (11p13), autosomal dominant
|
|
What is the mutation leading to retinoblastoma?
|
point mutation inactivates the RB gene --> no more suppression
|
|
Most variable phase in cell cycle
|
G1
|
|
G1 Phase of cell cycle
|
Synthesis of RNA, protein, organelles, and cyclin D; DNA repair; most variable phase
|
|
S Phase of cell cycle
|
Synthesis of DNA, RNA, protein; double the amount of genomic material
|
|
G2 Phase of cell cycle
|
Synthesis of tubulin, necessary for formation of the mitotic spindle
|
|
What happens in embryonic sexual differentiation when there is no Y chromosome?
|
Wolffian ducts --> apoptosis. The default pathway is to have keep the female structures.
|
|
What happens in embryonic sexual differentiation when there is a Y chromosome?
|
Sertoli cells make MIF (Mullerian inhibitory factor) --> Mullerian ducts --> apoptosis --> keep male structures.
|
|
Resistance transfer factor
|
plasmid that encodes one or more drug resistance genes & has capability of mediating its own transfer to another bacterium during conjugation.
|
|
How do transposons insert themselves into a new location?
|
site-specific recombination. Flanking DNA sequences of a transposon are indirect repeats that are complimentary and antiparallel to one another.
|
|
tra operon
|
Transfer operon. Genes necessary for non-sexual transfer of genetic material in bacteria.
|
|
Name two genetic mechanisms that can lead to either Angelman syndrome or Prader Willi.
|
Genomic imprinting or uniparental disomy.
|
|
Folic acid analog that inhibits dihydrofolate reductase
|
Methotrexate
|
|
Pyrimidine analog that inhibits thymidylate synthase
|
5-fluorouracil
|
|
Inhibitor of de novo purine synthesis
|
6-mercaptopurine
|
|
Inhibits DNA polymerase
|
cytarabine
|
|
Alkylating agents used to treat Non-Hodgkin lymphoma, breast and ovarian carcinoma.
|
Cyclophosphamide, ifosfamide
|
|
Alkylating agent capable of crossing blood brain barrier
|
Nitrosureas (carmustine, lomustine)
|
|
Similar to alkylating agent, notable toxicities include nephrotoxicity and acoustic nerve damage
|
Cisplatin, carboplatin
|
|
Alkylating agent used to treat CML
|
Busulfan
|
|
Free radical generator and also intercalates DNA to form strand breaks ("A" in ABVD treatment for Hodgkins)
|
Doxorubicin (Adriamycin), daunorubicin
|
|
Used to treat childhood tumors (Wilm's tumor, rhabdomyosarcoma, and Ewing's sarcoma)
|
Dactinomycin (Actinomycin D; Children ACT out)
|
|
Free radical generator which can cause life threatening pulmonary fibrosis
|
Bleomycin
|
|
Topoisomerase II inhibitor
|
Etoposide
|
|
Steroid that triggers apoptosis
|
Prednisone
|
|
Estrogen receptor antagonist
|
Tamoxifen
|
|
Monoclonal antibody against HER-2
|
Trastuzumab
|
|
Philadelphia chromosome bcr-abl tyrosine kinase inhibitor
|
Imatinib (Gleevec)
|
|
Binds tubulin blocking polymerization of microtubules and mitotic spindle formation
|
Vincristine, vinblastine
|
|
Binds tubulin hyperstabalizing microtubules and blocking mitotic spindle formation
|
Paclitaxel
|
|
Used for "metastatic" breast cancer
|
Trastuzumab
|
|
Increased risk of endometrial carcinoma
|
Tamoxifen
|
|
Do not use with allopurinol
|
6-mercaptopurine (activated by xanthine oxidase; allopurinol is a xanthine oxidase inhibitor used to treat gout)
|
|
CNS toxicity
|
Nitrosureas (carmustine, lomustine)
|
|
Neurotoxic (areflexia, peripheral neuritis) paralytic ileus
|
Vincristine (Vinblastine is notable for bone marrow suppression)
|
|
Antineoplastic used for therapeutic abortion
|
Methotrexate
|
|
Androgen receptor antagonist
|
Flutamide
|
|
Recombinantly produced cytokine used to treat hairy cell leukemia
|
Interferon alpha
|
|
GnRH agonist used for the treatment of metastatic prostate carcinoma
|
Leuprolide, Goserelin, Nafarelin
|
|
Monoclonal antibody against the protein CD20 used for treatment of low grade non-Hodgkin lymphoma
|
Rituximab
|
|
Aromatase inhibitor used to treat breast cancer
|
Anastrozole
|
|
In patients with impaired renal or hepatic function, how does loading does and maintenance dose change?
|
Loading dose remains unchanged Maintenance dose decreases
|
|
Phase I metabolism ;products, what happens and how eliminated
|
(reduction, oxidation, hydrolysis) yields slightly polar, water-soluble metabolites (often still active) not yet eliminated
|
|
Phase II metabolism ;products, what happens and how eliminated
|
acetylation, glucoronidation, sulfation) yields Very polar, inactive metanolites (renally excreted)
|
|
Geriatric patients lose which phase of metabolism first?
|
Phase I
|
|
pre and postsynaptic nervous system neurotransmitters;;Somatic
|
only one ;ACh (nicotinic)
|
|
pre and postsynaptic nervous system neurotransmitters;;Sympathetic
|
pre=ACh(nicotinic);Ach(muscarinic)-sweat glands; NEα,β-Cardiac and smooth muscle, gland cells, nerve terminals;D1-Renal vascular smooth muscle
|
|
nicotinic receptor mech
|
ACh ligand gated Na+/K+ channels
|
|
Release of NE from a sympathetic nerve ending is modulated by;;with mech
|
by NE itself, acting on presynaptic alpha-2 autoreceptors, and by ACh, ;;angiotensin II, and other substances.
|
|
Which Cholinergic Activates Bowel and Bladder smooth muscle;
|
Bethanechol
|
|
Which Cholinergic Contracts ciliary muscle of eye (open angle), pupillary sphincter (narrow angle)
|
Carbachol
|
|
Which Cholinergic Stimulates muscarinic receptors in airway when inhaled.
|
Methacholine
|
|
Which Cholinergic resistant to AChE
|
Bethanechol and Pilocarpine
|
|
Which Cholinergic ↑ endogenous ACh No CNS penetration
|
Neostigmine
|
|
Which Cholinergic ↑ endogenous ACh; ↑ strength
|
Pyridostigmine
|
|
Which Cholinergic is used for Postoperative and neurogenic ileus and urinary ;retention
|
Bethanechol ;and;Neostigmine
|
|
Which Cholinergic is used for Glaucoma, pupillary contraction, and release of intraocular pressure
|
Carbachol, Echothiophate and Physostigmine
|
|
Which Cholinergic is used for Potent stimulator of sweat, tears, saliva
|
Pilocarpine
|
|
Which Cholinergic is used for Challenge test for diagnosis of asthma
|
Methacholine
|
|
Which Cholinergic is used for reversal of ;neuromuscular junction blockade (postoperative)
|
Neostigmine
|
|
Which Cholinergic is used for Myasthenia gravis
|
Neostigmine ;;Pyridostigmine does penetrate CNS
|
|
Which Cholinergic is used for Diagnosis of myasthenia gravis
|
Edrophonium
|
|
Clinical applications of;;Bethanechol
|
Postoperative and neurogenic ileus and urinary ;retention
|
|
Clinical applications of;;Carbachol
|
Glaucoma, pupillary contraction, and release of ;intraocular pressure
|
|
Clinical applications of;;Pilocarpine
|
Potent stimulator of sweat, tears, saliva
|
|
Clinical applications of;;Methacholine
|
Challenge test for diagnosis of asthma
|
|
Clinical applications of;;Neostigmine
|
Postoperative and neurogenic ileus and urinary ;retention, myasthenia gravis, reversal of ;neuromuscular junction blockade (postoperative)
|
|
Clinical applications of;;Pyridostigmine
|
Myasthenia gravis; does penetrate CNS
|
|
Clinical applications of;;Edrophonium
|
Diagnosis of myasthenia gravis (extremely short ;acting)
|
|
Clinical applications of;;Physostigmine
|
Glaucoma (crosses blood-brain barrier ? CNS) ;and atropine overdose
|
|
Clinical applications of;;Echothiophate
|
Glaucoma
|
|
Cholinesterase inhibitor poisoning;;symptoms
|
Diarrhea, Urination, Miosis, Bronchospasm, Bradycardia, Excitation of skeletal muscle and CNS, Lacrimation, Abdominal cramping, Sweating
|
|
pralidoxime;;uses and mech
|
Cholinesterase inhibitor poisoning;;chemical antagonist used to regenerate active cholinesterase
|
|
Parathion
|
organophosphate
|
|
Ipratropium ;;mech
|
Muscarinic antagonist
|
|
Methscopolamine, ;oxybutin, ;glycopyrrolate ;;mech
|
Muscarinic antagonist
|
|
Atropine;;clinical use
|
Produce mydriasis and cycloplegia
|
|
Benztropine ;;clinical use
|
Parkinson's disease
|
|
Ipratropium ;;clinical use
|
Asthma, COPD
|
|
Methscopolamine, ;oxybutin, ;glycopyrrolate ;;clinical use
|
Reduce urgency in mild cystitis and reduce bladder spasms
|
|
Glaucoma drugs mech and side effects;;Epinephrine
|
↑ outflow of aqueous humor ;;Mydriasis, stinging; do not use;in closed-angle glaucoma
|
|
Glaucoma drugs mech and side effects;;Brimonidine
|
↓ aqueous humor synthesis ;;No pupillary or vision changes
|
|
Glaucoma drugs mech and side effects;;beta-blockers
|
↓ aqueous humor secretion ;;No pupillary or vision changes
|
|
Glaucoma drugs mech and side effects;;Acetazolamide
|
↓ aqueous humor secretion due to ;↓ HCO3- (via inhibition of carbonic anhydrase);;No pupillary or vision changes
|
|
Glaucoma drugs mech and side effects;;Cholinomimetics
|
↑ outflow of aqueous humor; contract ciliary muscle and open trabecular meshwork;;;Miosis, cyclospasm
|
|
Glaucoma drugs mech and side effects;;Latanoprost (PGF2α)
|
↑ outflow of aqueous humor;;Darkens color of iris (browning)
|
|
Atropine effects
|
dilates pupils and Blocks SLUD: ;↓Salivation;↓Lacrimation;↓Urination;↓Defecation
|
|
Can cause acute angle-closure glaucoma in elderly, urinary retention in men with prostatic hypertrophy.
|
Atropine
|
|
Hexamethonium;;Clinical use
|
Ganglionic blocker. Used in experimental models to prevent vagal reflex responses to ;changes in blood pressure
|
|
Mechanism for Sympathomimetics;;Ephedrine
|
Indirect general agonist, releases stored ;catecholamines
|
|
Mechanism for Sympathomimetics;;Cocaine
|
Indirect general agonist, uptake inhibitor
|
|
Mechanism for Sympathomimetics;;Clonidine, α-methyldopa
|
Centrally acting α-agonist, ↓ central ;adrenergic outflow
|
|
What drugs cause Cardiovascular Atropine-like side effects
|
Tricyclics
|
|
What drugs cause Cardiac toxicity
|
Doxorubicin (Adriamycin), daunorubicin
|
|
What drugs cause Coronary vasospasm
|
Cocaine
|
|
What drugs cause Cutaneous rushing
|
Niacin, Ca2+ channel blockers, adenosine, vancomycin
|
|
What drugs cause Torsades des pointes
|
Class III (sotalol), class IA (quinidine), cisapride
|
|
What drugs cause Agranulocytosis
|
Clozapine, carbamazepine, colchicine
|
|
What drugs cause Aplastic anemia
|
Chloramphenicol, benzene, NSAIDs
|
|
What drugs cause Acute cholestatic ;hepatitis
|
Macrolides
|
|
What drugs cause Focal to massive ;hepatic necrosis
|
Halothane, valproic acid, acetaminophen, Amanita phalloides
|
|
What drugs cause Hepatitis
|
INH
|
|
What drugs cause Hot rashes
|
Tamoxifen
|
|
What drugs cause Gingival hyperplasia
|
Phenytoin
|
|
What drugs cause Osteoporosis
|
Corticosteroids, heparin
|
|
What drugs cause Photosensitivity
|
(SAT for a photo) Sulfonamides, Amiodarone, Tetracycline
|
|
What drugs cause Fanconi's syndrome
|
Expired tetracycline
|
|
What drugs cause Interstitial nephritis
|
Methicillin
|
|
What drugs cause Hemorrhagic cystitis
|
Cyclophosphamide, ifosfamide
|
|
What drugs cause Cinchonism
|
Quinidine, quinine
|
|
What drugs cause Diabetes insipidus
|
Lithium, demeclocycline
|
|
What drugs cause Disulfram-like reaction
|
Metronidazole, certain cephalosporins, procarbazine, sulfonylureas
|
|
What drugs cause Nephrotoxicity & neurotoxicity
|
Polymyxins
|
|
What drugs cause Nephrotoxicity & ototoxicity
|
Aminoglycosides, loop diuretics, cisplatin
|
|
P-450 Inducer
|
Quinidine (can inhibit too), Barbiturates, Phenytoin, Rifampin, Griseofulvin, Carbamazepine, St. John?s wort
|
|
P-450 Inhibitors
|
Isoniazid; Sulfonamides; Cimetidine; Ketoconazole; Erythromycin; Grapefruit juice
|
|
Iron Poisioning Symps
|
acute gastric bleeding chronic metabolic acidosis, scarring (leading to GI obstruction)
|
|
Ethylene glycol toxicity
|
Acidosis, nephrotoxicity
|
|
Methanol toxicity
|
Severe acidosis, retinal damage
|
|
Too much Ethylene glycol can cause what compound to build up?
|
Build up of Oxalic acid
|
|
Too much Methanol can cause what compound to build up?
|
Build up of Formaldehyde;and formic acid
|
|
Drugs that cause problems in patients with sulfa allergies
|
Celecoxib, furosemide, thiazides, TMPSMX, sulfonyureas, sufasalazine
|
|
Herbal agents Clinical uses and Toxicities Echinacea
|
Common cold; no major toxicities
|
|
Herbal agents Clinical uses and Toxicities Ephedra
|
Same as ephedrine; CNS and cardiovascular stimulation; arrhythmias, stroke, and seizures at high doses
|
|
Herbal agents Clinical uses and Toxicities Feverfew
|
Used for migraine. Adv: mouth ulcers, antiplatelet actions
|
|
Herbal agents Clinical uses and Toxicities Ginkgo
|
Used for Intermittent claudication. Adv: anxiety, insomnia, antiplatelet actions
|
|
Herbal agents Clinical uses and Toxicities Kava
|
Used for Chronic anxiety. Adv: sedation, ataxia, hepatotoxicity, phototoxicity, dermatotoxicity
|
|
Herbal agents Clinical uses and Toxicities Milk thistle
|
Used for Viral hepatitis. Adv: Loose stools
|
|
Herbal agents Clinical uses and Toxicities Saw palmetto
|
Used for Benign prostatic hyperplasia. Adv: ↓ libido, hypertension
|
|
Herbal agents Clinical uses and Toxicities St. John's wort
|
Used for Mild to moderate depression. Adv: phototoxicity; serotonin syndrome;with SSRIs; induces P450 system
|
|
Herbal agents Clinical uses and Toxicities Dehydroepiandrosterone
|
Used for Symptomatic improvement in females with SLE or AIDS Androgenization (premenopausal), estrogenic effects (postmenopausal), feminization
|
|
Herbal agents Clinical uses and Toxicities Melatonin
|
Used for Jet lag and insomnia. Adv: Sedation, suppresses midcycle LH, hypoprolactinemia
|
|
Drug name Ending / Category -afil
|
Erectile dysfunction
|
|
Drug name Ending / Category -phylline
|
Methylxanthine
|
|
selectivity for Sympathomimetics - Albuterol
|
β2 >β1
|
|
Mechanism/selectivity for Sympathomimetics - terbutaline
|
β2 >β1
|
|
Applications of Sympathomimetics - Amphetamine
|
Narcolepsy, obesity, ADHD
|
|
Applications of Sympathomimetics - Ephedrine
|
Nasal decongestion, urinary incontinence, hypotension
|
|
Applications of Sympathomimetics - Phenylephrine
|
Pupil dilator, vasoconstriction, nasal decongestion
|
|
Applications of Sympathomimetics - Albuterol, terbutaline
|
Asthma
|
|
Applications of Sympathomimetics - Clonidine, α-methyldopa
|
Hypertension, especially with;renal disease (no ↓ in blood ;flow to kidney)
|
|
name the α2 selective α-blockers
|
Mirtazapine
|
|
Nonselective α-blockers - Application and Toxicity
|
Pheochromocytoma - Orthostatic hypotension, reflex tachycardia
|
|
α1 selective α-blockers - Application and Toxicity
|
Hypertension, urinary retention in BPH - -1st-dose orthostatic hypotension, dizziness, headache
|
|
α2 selective α-blockers - Application and Toxicity
|
Depression - Sedation, ↑ serum cholesterol, ↑ appetite
|
|
Nonselective α-blockers - names and differences
|
Phenoxybenzamine (irreversible) - phentolamine (reversible)
|
|
β-blockers - non selective ones
|
propranolol, timolol, nadolol, pindolol (partial agonist), and - labetalol (partial agonist, and exception to rules)
|
|
β-blockers - selective ones
|
Betaxolol, Esmolol (short acting), Atenolol, Metoprolol - Acebutolol (partial agonist hes and Ass),
|
|
which β-blockers - Tx for Glaucoma
|
timolol
|
|
which β-blockers - Tx for SVT
|
propranolol, esmolol
|
|
β-blockers - Toxicity (non cardiac)
|
1. Impotence, 2. exacerbation of asthma, 3. CNS adverse effects (sedation, sleep alterations), 4. diabetics can't feel low sugar
|
|
block Na+ channel; inhibit glutamate release
|
phenytoin
|
|
increase DURATION of Cl- channel opening --> increase GABA(A) action
|
barbiturates
|
|
increase FREQUENCY of Cl- channel opening --> increase GABA(A) action
|
BZD
|
|
for detox, especially EtOH withdrawal (DT), night terrors, sleepwalking
|
BZD
|
|
additive CNS depression effects with EtOH
|
barbiturates, BZD
|
|
SE: nystagmus, diplopia, SLE-syndrome, increases P450
|
phenytoin
|
|
anti-seizure drugs also used for bipolar treatment
|
carbamazepine, lamotrigine, valproic acid
|
|
1st line for tonic-clonic seizures
|
phenytoin, carbamazpine, valproic acid
|
|
1st line for status epilepticus prophylaxis
|
phenytoin
|
|
anti-seizure drugs also used for peripheral neuropathy
|
gabapentin
|
|
1st line for epilepsy in pregnancy and children
|
phenobarbital
|
|
also used for myoclonic seizures
|
valproic acid
|
|
also used for eclampsia seizures
|
BZD
|
|
1st line to prevent eclampsia seizures
|
MgSO4
|
|
increase Na+ channel inactivation
|
phenytoin, carbamazepine, valproic acid
|
|
blocks voltage gated Na+ channels
|
lamotrigine
|
|
increase GABA release
|
gabapentin
|
|
increase GABA(A) action
|
phenobarbital, BZD
|
|
increase [GABA]
|
valproic acid
|
|
drugs a/w Steven Johnson syndrome
|
ethosuxamide, lamotrigine, phenytoin, phenobarbital
|
|
most common drugs for endoscopy
|
midazolam (BZD)
|
|
stimulates heart, increases cerebral blood flow, for kids < 13 y/o
|
ketamine
|
|
non-depolarzing neuromuscular blocking drug --> competes with ACh
|
tubocurarine, atracurium, mivacurium, pancuronum, vecuronium, rocuronium
|
|
inhibit MAO-B ---> prevents DA breakdown in brain
|
selegiline
|
|
5HT(1D) agonist --> causes vasoconstriction
|
sumatriptan
|
|
used for acute migraines, cluster headaches
|
sumatriptan
|
|
atypical anti psychotics
|
clozapine, olanzapine, risperidone, apripazole, quetiapine
|
|
SSRIs
|
fluoxetine, sertraline, paroxetine, citalopram
|
|
TCAs
|
impramine, amytriptyline
|
|
MAOIs
|
phenelzine, selegiline, tranylcyprome
|
|
EtOH withdrawal treatment
|
BZD
|
|
anorexia/bulimia treatment
|
SSRI
|
|
atypical depression
|
MAOI
|
|
bipolar treatment
|
mood stabilizers: lithium, valproic acid, carbamazepine
|
|
depression treatment
|
SSRI, TCA
|
|
depression with insomnia treatment
|
trazadone (increases REM), mirtazapine (causes sedation)
|
|
OCD treatment
|
SSRI, clomipramine (TCA)
|
|
panic disorder treatment
|
TCA, busprione
|
|
Tourette's treatment
|
haloperidol, olanzapine (atypical antipyschotic)
|
|
blocks D2 receptors
|
antipsychotics (neuroleptics); D2 normally regulates NT release
|
|
block DA and 5HT(2) receptors
|
atypical antipsyhotics
|
|
inhibit phosphoninositol cascade
|
lithium
|
|
stimulates 5HT(1A) receptor
|
busprione
|
|
blocks NE and 5HT reuptake
|
TCA
|
|
block DA, NE, 5HT reuptake
|
venlafaxine
|
|
alpha-2 antag --> increase NE and 5HT release; 5HT(2) and 5HT(3) receptor antag
|
mirtazapine
|
|
blocks NE uptake
|
maprotiline
|
|
inhibit 5HT reuptake
|
trazadone
|
|
EPS side effects
|
4 hours dystonia, 4 days akinesia (parkinsonism), 4 weeks akathesia (restlessness), 4 months tardive dyskinesia
|
|
neuroleptic malignant syndrome
|
rigidity, myoglobinuria, autonomic instability, hyperpyrexia
|
|
OCD, anxiety, depression, mania, Tourette's treatment
|
olanzapine
|
|
SE: tremor, nephrogenic DI, hypoTN, pregnancy problems
|
lithium
|
|
anxiolysis for generalized anxiety disorder; no sedation or addiction, no interaction with EtOH
|
busprione
|
|
serotonin syndrome
|
hyperthermia, muscle rigidity, CV collapse
|
|
SE: convulsions, coma, cardiotoxicity
|
TCAs
|
|
used in smoking cessation
|
bupropion
|
|
antidepressant that does NOT cause sexual SE
|
bupropion
|
|
SE: increase REM, priapism
|
trazadone
|
|
treatment for depressed elderly patient who is losing weight
|
mirtazapine (SE: increased appetite)
|
|
contraindicated in treatement of depressed bulimic patient
|
bupropion --> decreases seizure threshold
|
|
contraindicated with tyramine ingestion and B-agonists --> hyperthermia
|
MAOI
|
|
contraindicated with SSRI and meperidine --> serotonin syndrome
|
MAOI
|
|
What type of graft is from an identical twin sibling?
|
Syngeneic graft
|
|
What type of graft is from the same species?
|
Allogenic or homograft
|
|
What type of graft is taken from a different species?
|
heterograft (also called xenogenic graft)
|
|
Mitochondrial poisons
|
damages membrane and drains off protons; alcohol, salicylates
|
|
Complication of mitochondrial poisons/uncoupling agents
|
hyperthermia
|
|
Decreased ATP
|
impaired Na+/K+ ATPase pump (cellular swelling); reversible
|
|
Irreversible injury hypoxia
|
membrane/mitochondrial damage
|
|
Mitochondrial damage
|
release cytochrome c activates apoptosis
|
|
Irreversible injury hypoxia
|
increase cytosolic Ca2+ activates phospholipase, proteases, endonuclease
|
|
SER hyperplasia
|
alcohol, barbiturates, phenytoin
|
|
Complications SER hyperplasia
|
increases drug metabolism (e.g., oral contraceptives); low vitamin D
|
|
Chediak-Higashi
|
membrane protein defect in transferring lysosomal enzymes to phagocytic vacuoles; AR; giant lysosomes
|
|
Rigor mortis
|
stiff muscles after death due to ATP depletion
|
|
Hemosiderin
|
insoluble ferritin degradation product visible with Prussian blue stain
|
|
Labile cells
|
stem cells (skin, marrow, GI tract)
|
|
Stable cells
|
in G0 phase (smooth muscle, hepatocytes); can enter cell cycle (growth factors, hormones)
|
|
Prostate hyperplasia
|
increased dihydrotestosterone (DHEA)
|
|
Squamous metaplasia bladder
|
Schistosoma hematobium infection
|
|
Dysplasia
|
atypical hyperplasia and metaplasia are precursors for cancer
|
|
Granulomas
|
activated macrophages (epithelioid cells); multinucleated giant cells; CD4 TH1 cells, type IV hypersensitivity
|
|
Epithelioid cells
|
γ-interferon released by CD4 T cells activates macrophages
|
|
Multinucleated giant cells
|
fusion of epithelioid cells
|
|
Enzymatic fat necrosis
|
associated with pancreatitis; soap formation (Ca2+ + fatty acids)
|
|
Fibrinoid necrosis
|
necrosis of immune reactions (immune vasculitis/endocarditis)
|
|
Postmortem necrosis
|
autolysis; no inflammatory reaction
|
|
Dystrophic calcification
|
calcification of damaged tissue; normal serum calcium; pancreatitis; atherosclerotic plaque
|
|
Nephrocalcinosis
|
metastatic calcification of collecting tubule basement membranes; polyuria due to nephrogenic diabetes insipidus; renal failure
|
|
Caspases
|
responsible for enzymatic cell death in apoptosis; proteases and endonucleases
|
|
Markers of apoptosis
|
eosinophilic cytoplasm, pyknotic (ink dot) nucleus
|
|
Histamine
|
key chemical in acute inflammation; mast cell; arteriole vasodilation; increase venular permeability
|
|
Rubor acute inflammation
|
redness; arteriole vasodilation (histamine)
|
|
Calor acute inflammation
|
heat; arteriole vasodilation (histamine)
|
|
Tumor acute inflammation
|
swelling; increase vessel permeability (histamine)
|
|
Dolor acute inflammation
|
pain; bradykinin, PGE
|
|
Acute inflammation
|
neutrophil dominant; increase IgM
|
|
Chronic inflammation
|
monocyte/macrophage; increase IgG; repair by fibrosis
|
|
Positive PPD
|
Langerhan's cells process PPD and interact with TH1 class cells
|
|
Suppurative inflammation
|
abscess; Staphylococcus aureus (coagulase)
|
|
Cellulitis
|
subcutaneous inflammation; Streptococcus pyogenes (hyaluronidase)
|
|
Pseudomembranous inflammation
|
toxins from Corynebacterium diphtheriae, Clostridium difficile
|
|
BAX gene
|
stimulates apoptosis; activated by TP53 suppressor gene if too much DNA damage
|
|
Extracellular matrix
|
basement membrane, interstitial matrix
|
|
Complete restoration
|
cell must be capable of duplication, no damage to basement membrane
|
|
Liver injury
|
regenerative nodules; abnormal cytoarchitecture
|
|
CNS injury
|
astrocyte and microglial cell repair cells; gliosis
|
|
WBC alterations in acute inflammation
|
neutrophilic leukocytosis, left shift, toxic granulation
|
|
Erythrocyte sedimentation rate
|
increased fibrinogen enhances rouleaux
|
|
C-reactive protein
|
indicator of acute inflammation and inflammatory atheromatous plaque
|
|
Total body water
|
ECF (plasma, interstitial fluid) + ICF (cytosol)
|
|
Lymphedema
|
radical mastectomy; filariasis; inflammatory carcinoma (lymphatics plugged by tumor)
|
|
Lipofuscin
|
indigestible lipid of lipid peroxidation; brown pigment increased in atrophy and FR damage
|
|
O2-dependent MPO system
|
most potent microbicidal system; neutrophils, monocytes
|
|
Production of superoxide from O2
|
NADPH oxidase with NADPH cofactor; produces respiratory burst
|
|
Nitro blue tetrazolium (NBT)
|
test for respiratory burst
|
|
Superoxide dismutase
|
converts superoxide to peroxide
|
|
Myeloperoxidase
|
lysosomal enzyme that combines peroxide + Cl to form bleach (HOCl)
|
|
Microbicidal defects
|
chronic granulomatous disease childhood (XR), myeloperoxidase deficiency (AR)
|
|
Inspiration
|
increases right sided abnormal heart sounds and murmurs
|
|
Expiration
|
increases left sided abnormal heart sounds and murmurs
|
|
Familial hypercholesterolemia (type II)
|
AD; deficiency of LDL receptors; increase LDL
|
|
Type III hyperlipoproteinemia
|
deficiency apo E; increase remnants (chylomicron, intermediate density)
|
|
Type IV hyperlipoproteinemia
|
increase VLDL; alcoholics
|
|
Apo B deficiency
|
deficiency apo B48 (chylomicrons) and B100 (VLDL); decrease CH and TG
|
|
Clinical findings in apo B deficiency
|
malabsorption; hemolytic anemia
|
|
Cardiovascular Risk factors
|
smoking, increase LDL, increase homocysteine, Chlamydia pneumoniae infection
|
|
Cells involved in atherosclerosis
|
platelets, macrophages, smooth muscle cells, T cells with cytokine release
|
|
Increased plasma homocysteine
|
increase vessel thrombosis; folate (MC)/vitamin B12 deficiency
|
|
Hyaline arteriolosclerosis
|
small vessel disease of DM and hypertension; excess protein in vessel wall
|
|
Mechanisms hyaline arteriolosclerosis in DM
|
non-enzymatic glycosylation
|
|
Non-enzymatic glycosylation
|
glucose attaches to amino acids in BM; causes increase permeability to protein
|
|
Mechanisms hyaline arteriolosclerosis in hypertension
|
pressure pushes proteins into vessel wall
|
|
Cystic medial degeneration
|
elastic tissue degeneration creates spaces filled with mucopolysaccharides
|
|
Intimal tear in aorta
|
due to wall stress from hypertension and structural weakness
|
|
Types of dissection
|
proximal (MC); distal or combination of both
|
|
S/S proximal aortic dissection
|
chest pain radiating to back, lack of pulse; cardiac tamponade MC COD
|
|
Phlebothrombosis
|
stasis of blood flow; deep veins below knee MC site
|
|
Superficial migratory thrombophlebitis
|
sign of carcinoma of head of pancreas
|
|
Thoracic outlet syndrome
|
absent radial pulse with positional change
|
|
Bacillary angiomatosis
|
Bartonella henselae; vascular infection in AIDS
|
|
Muscular artery vasculitis
|
vessel thrombosis with infarction; e.g., classical polyarteritis nodosa
|
|
Elastic artery vasculitis
|
absent pulse, stroke
|
|
Giant cell arteritis
|
temporal artery granulomatous vasculitis; ipsilateral blindness (ophthalmic artery)
|
|
Classical polyarteritis nodosa
|
muscular artery vasculitis with vessel thrombosis infarction
|
|
Path findings for Classical polyarteritis nodosa
|
vessel inflammation at different stages; aneurysms from vessel weakness
|
|
S/S Classical polyarteritis nodosa
|
infarctions in kidneys, skin, GI tract, heart; HBsAg in 30%
|
|
Kawasaki‘s disease
|
coronary artery vasculitis/thrombosis/aneurysms in children
|
|
S/S Kawasaki's disease
|
chest pain; desquamating rash; swelling hands/feet; cervical lymphadenopathy
|
|
Rx for Kawasaki's disease
|
IV y-globulin
|
|
Cryoglobulinemia
|
protein gels in cold temperature; Raynaud's syndrome; HCV association
|
|
S/S Cryoglobulinemia
|
acral cyanosis relieved by coming indoors
|
|
Microscopic polyangiitis
|
palpable purpura; crescentic GN; association with p-ANCA
|
|
Henoch-Schönlein purpura
|
IgA-anti-IgA ICs; palpable purpura buttocks/legs; arthritis; IgA GN
|
|
Serum sickness vasculitis
|
e.g., horse antivenin in Rx of rattlesnake envenomation
|
|
Meningococcemia
|
sepsis causes petechia/ecchymoses; potential for Waterhouse Friderichsen syndrome
|
|
Renovascular HTN
|
atherosclerosis renal artery in men; fibromuscular hyperplasia renal artery women
|
|
Endocrine HTN
|
1° HPTH, Graves/hypothyroidism, Cushing's, 1° aldosteronism, phaeochromocytoma
|
|
AMI ruptures
|
3rd-7th day
|
|
Posteromedial papillary muscle rupture
|
RCA thrombosis; mitral regurgitation with LHF
|
|
S/S Pericarditis
|
friction rub; leaning forward relieves pain
|
|
Right ventricular infarction
|
RCA thrombosis; hypotension, RHF, preserved left ventricular function
|
|
Reinfarction
|
reappearance CK-MB after 3 days
|
|
Complications cyanotic heart disease
|
2° polycythemia; infective endocarditis; metastatic abscesses
|
|
S/S Post-ductal coarctation
|
upper extremity HTN; claudication; rib-notching; activation RAA also causes HTN
|
|
Acute rheumatic fever
|
type II hypersensitivity; group A streptococcus pharyngeal infection; sterile vegetations mitral valve (regurgitation); myocarditis with Aschoff nodule
|
|
S/S MVP
|
mid-systolic click followed by a murmur; palpitations, chest pain, rupture of chordae
|
|
MVP click/murmur close to S1
|
decrease preload (stand, Valsalva, anxiety)
|
|
MVP click/murmur close to S2
|
increase preload (supine, squat, clench fist)
|
|
Causes of Mitral regurgitation
|
LHF, infective endocarditis, acute rheumatic fever
|
|
Austin Flint murmur
|
diastolic murmur; regurgitant flow on anterior leaflet mitral valve
|
|
Significance Austin Flint murmur
|
sign for Aortic V replacement
|
|
Causes of Tricuspid regurgitation
|
endocarditis IV drug abuse; RHF; carcinoid heart disease
|
|
Carcinoid heart disease
|
tricuspid regurgitation, pulmonic stenosis
|
|
Infective endocarditis (IE)
|
Streptococcus viridans MCC; Staphylococcus aureus MCC IVDA
|
|
Infective endocarditis in ulcerative bowel disease
|
Streptococcus bovis
|
|
Parasitic cause myocarditis
|
leishmania in Chagas disease
|
|
S/S Pericardial effusion
|
muffled heart sounds, pulsus paradoxus, inspiratory neck vein distention
|
|
Causes Congestive cardiomyopathy
|
postpartum, cardiotoxic drugs, hypothyroidism, alcohol
|
|
Causes of Restrictive cardiomyopathy
|
iron, amyloid, glycogen; sarcoidosis; tropical endocardial fibrosis
|
|
Cardiac rhabdomyoma
|
childhood tumor; association with tuberous sclerosis
|
|
U wave
|
hypokalemia; MCC diuretic therapy (e.g., thiazides; loop diuretics)
|
|
Peaked T wave
|
hyperkalemia; MCC renal failure
|
|
Causes fatty change in liver
|
increase synthesis TG/FAs, beta-oxidation of FAs, synthesis apoproteins/release VLDL
|
|
Fatty change in kwashiorkor
|
decrease synthesis of apoproteins
|
|
Hairy leukoplakia
|
EBV glossitis; pre-AIDS defining lesion; not precursor to cancer
|
|
Mumps
|
bilateral parotitis; unilateral orchitis; increase amylase
|
|
Exudative tonsillitis
|
majority are viral; 20% group A streptococcus
|
|
Oral thrush
|
common in newborn; pre-AIDS defining lesion; yeasts and pseudohyphae
|
|
Peutz-Jegher's syndrome
|
mucosal pigmentation; hamartomatous polyps
|
|
Leukoplakia/erythroleukoplakia
|
biopsy to rule out squamous dysplasia or cancer
|
|
Squamous cell carcinoma
|
smoking and alcohol association; lower lip MC site
|
|
Smokeless tobacco
|
verrucoid squamous cell carcinoma
|
|
Gum hyperplasia
|
phenytoin, pregnancy, scurvy
|
|
Pleomorphic adenoma
|
MC benign tumor of salivary glands; parotid MC site
|
|
Mucoepidermoid carcinoma
|
MC malignant tumor major and minor salivary glands
|
|
AIDS esophagitis
|
Candida MC, CMV, HSV
|
|
Hamman's mediastinal crunch
|
pneumomediastinum (air in subcutaneous tissue)
|
|
LES ganglion cells
|
contain VIP - relaxes LES
|
|
Achalasia
|
failure of LES relaxation (no VIP); absent ganglion cells in the myenteric plexus
|
|
Acquired achalasia
|
Chagas' disease; leishmania destroy ganglion cells
|
|
Congenital pyloric stenosis
|
hypertrophy pyloric muscle; vomiting non-bile stained fluid in 2-4 weeks
|
|
Acute hemorrhagic (erosive) gastritis
|
NSAIDs MCC
|
|
Type A chronic gastritis
|
due to PA; achlorhydria with increase serum gastrin
|
|
Type B chronic gastritis
|
due to H. pylori; involves pylorus and antrum
|
|
Gastric ulcer
|
lesser curvature pylorus and antrum; poor defense against acid; food aggravates pain
|
|
Perforated peptic ulcer
|
air under diaphragm causes pain in left shoulder
|
|
Menetrier's disease
|
giant rugal hyperplasia; protein loss from increased mucus
|
|
Hypergastrinemia
|
ZE, achlorhydria, gastric distention, H2 or proton blockers; renal failure
|
|
Malabsorption
|
steatorrhea; chronic pancreatitis, bile salt deficiency, small bowel disease
|
|
Causes bile salt deficiency
|
liver disease, bile salt resins, cholestasis, bacterial overgrowth, Crohn's
|
|
D-xylose screen
|
failure to reabsorb xylose indicates small bowel disease
|
|
Calcification of pancreas
|
chronic pancreatitis cause of malabsorption
|
|
Invasive diarrhea
|
Campylobacter jejuni MCC; positive fecal smear for leukocytes
|
|
Rotavirus
|
MCC diarrhea in children
|
|
Norwalk virus
|
MCC diarrhea in adults
|
|
Cytomegalovirus
|
common cause diarrhea in AIDS; MCC cholecystitis and pancreatitis in AIDS
|
|
Shigella sonnei
|
produces dysentery (bloody diarrhea); associated with HUS
|
|
Salmonella enteritidis
|
gastroenteritis; animal reservoirs - poultry, turtles
|
|
Salmonella paratyphi
|
sepsis; osteomyelitis in HbSS
|
|
Salmonella typhi
|
typhoid fever; human transmission; bradycardia, neutropenia, splenomegaly
|
|
Carrier state site of salmonella
|
gallbladder
|
|
M. tuberculosis
|
MCC intestinal TB in United States (swallow TB); Peyer's patch site of infection
|
|
Enterotoxigenic E. coli
|
secretory diarrhea (traveler's diarrhea); toxin stimulates guanylate cyclase
|
|
Yersinia enterocolitica
|
mesenteric lymphadenitis; sepsis in iron overload states
|
|
Entamoeba histolytica
|
dysentery; trophozoites phagocytose RBCs; liver abscess; Rx metronidazole
|
|
Cryptosporidium parvum
|
MCC diarrhea in AIDS; acid-fast oocysts
|
|
Trichuris trichiura
|
rectal prolapse in children
|
|
Enterobius vermicularis
|
anal pruritus; urethritis in girls; no eosinophilia
|
|
Necator americanus
|
hookworm; iron deficiency anemia
|
|
Strongyloides stercoralis
|
rhabditiform larvae in stool not eggs
|
|
Diphyllobothrium latum
|
fish tapeworm; vitamin B12 deficiency
|
|
Signs of small bowel obstruction
|
colicky pain; constipation and obstipation
|
|
Radiograph in small bowel obstruction
|
air-fluid levels on x-ray
|
|
MCC small bowel obstruction
|
adhesions from previous surgery
|
|
Duodenal atresia
|
vomiting bile-stained fluid at birth; double bubble sign; Down syndrome
|
|
Hirschsprung association
|
Down syndrome; Chagas disease
|
|
Meconium ileus
|
complication of cystic fibrosis
|
|
Indirect inguinal hernia
|
second MCC of small bowel obstruction; common in weight lifting
|
|
Gallstone ileus
|
obstruction of small bowel with gallstone + air in biliary tree
|
|
Volvulus
|
MC due to sigmoid colon twisting around mesentery
|
|
Direct inguinal hernia
|
protrudes through center of triangle of Hesselbach; no obstruction
|
|
Umbilical hernia
|
common in black children; may entrap bowel in adults
|
|
Small bowel infarction
|
diffuse abdominal pain with bloody diarrhea
|
|
Causes small bowel infarction
|
embolism (atrial fibrillation), thrombosis SMA or SMV
|
|
Ischemic colitis
|
splenic flexure pain with bloody diarrhea
|
|
Mesenteric angina
|
pain in splenic flexure 30 minutes after eating
|
|
Angiodysplasia
|
submucosal dilation of venules in cecum; cause of hematochezia
|
|
Hematochezia
|
massive loss of blood per rectum; diverticulosis MCC
|
|
Meckel's diverticulum
|
persistence omphalomesenteric duct; mimics acute appendicitis; cannot differentiate without radionuclide scan
|
|
S/S Meckel's diverticulum
|
bleeding MC (iron deficiency in children), diverticulitis
|
|
Sigmoid diverticulum
|
diverticulitis MC complication; MCC hematochezia and fistula formation
|
|
Diverticulitis
|
left-sided acute appendicitis
|
|
Ulcerative colitis associations
|
primary sclerosing cholangitis, seronegative HLA B27 + spondyloarthropathy
|
|
Carcinoid tumor
|
appendix MC site; terminal ileum MC site for carcinoid syndrome
|
|
Carcinoid syndrome
|
liver metastasis; flushing/diarrhea due to serotonin; increased urine 5-HIAA
|
|
Tubular adenomas
|
precursor lesion colon cancer; size and number determine risk of malignancy
|
|
Villous adenoma
|
greatest risk for colon cancer (30%); secrete mucus rich in protein and potassium
|
|
Turcot's syndrome
|
AD, polyposis plus brain tumors
|
|
Acute appendicitis
|
due to lymphoid hyperplasia in children and obstruction by fecalith in adults
|
|
External hemorrhoids
|
thrombose
|
|
Internal hemorrhoids
|
bleed; prolapse out of rectum
|
|
Alcoholic liver disease
|
serum AST>ALT; increase serum GGT
|
|
Cholestasis markers
|
serum AP and GGT
|
|
% Conjugated bilirubin <20%
|
Gilberts, spherocytosis, physiologic jaundice newborn, ABO/Rh HDN
|
|
Gilbert's disease
|
AD; decrease uptake and conjugation; bilirubin increases with fasting
|
|
% Conjugated bilirubin 20-50%
|
viral/alcoholic hepatitis
|
|
% Conjugated bilirubin >50%
|
bile duct obstruction (intra or extrahepatic); carcinoma head of pancreas
|
|
Negative urine bilirubin + trace urobilinogen
|
normal urine
|
|
Positive urine bilirubin, absent urobilinogen
|
obstructive jaundice
|
|
Positive urine bilirubin + increased urobilinogen
|
hepatitis
|
|
Negative urine bilirubin + increased urobilinogen
|
extravascular hemolytic anemia
|
|
Markers of severity of liver disease
|
albumin, PT
|
|
Anti-HBs + anti-HBc-IgG
|
recovered from HBV
|
|
HBsAg + HBeAg + HBVDNA + anti-HBc-IgM
|
acute HBV/chronic HBV infective carrier if >6 months
|
|
Anti HBc-IgM alone
|
serologic gap; not infective
|
|
HBsAg + anti-HBc-IgM
|
chronic HBV healthy carrier
|
|
Fulminant hepatic failure
|
viral hepatitis and acetaminophen MCCs
|
|
Spontaneous peritonitis
|
E. coli in adults; S. pneumoniae in children; complication of ascites
|
|
Granulomatous hepatitis
|
TB MC bacteria
|
|
Schistosomiasis
|
Schistosoma mansoni; adult worms in portal vein; "pipe stem cirrhosis"
|
|
Hypertriglyceridemia in alcoholics
|
increase synthesis of glycerol 3P (substrate for TG synthesis)
|
|
Ketoacidosis in alcoholics
|
increase lactate, increase β-HOB (acetyl CoA converted to AcAc and then β-HOB)
|
|
Primary sclerosing cholangitis
|
association with ulcerative colitis; MCC of cholangiocarcinoma
|
|
Extrahepatic biliary atresia
|
neonatal cholestasis
|
|
Drugs causing hepatitis
|
acetaminophen, isoniazid, halothane
|
|
Anabolic steroids
|
intrahepatic cholestasis
|
|
Estrogen/oral contraceptives
|
intrahepatic cholestasis; hepatic adenoma (intraperitoneal hemorrhage)
|
|
Methotrexate
|
liver fibrosis, fatty change
|
|
Liver angiosarcoma
|
vinyl chloride
|
|
S/S Hemochromatosis
|
cirrhosis; "bronze diabetes" - skin pigmentation + destruction of islet cells; malabsorption
|
|
Lab Hemochromatosis
|
increase serum ferritin, iron, % saturation; decrease TIBC
|
|
Alpha-1 antitrypsin deficiency in child
|
AR, cannot secrete AAT from liver cell; cirrhosis; hepatocellular carcinoma
|
|
Causes cirrhosis
|
alcohol (MC), HBV/HCV, hemochromatosis, Wilson's, AAT deficiency, 1° biliary
|
|
Cause of ascites
|
portal hypertension; hypoalbuminemia; secondary aldosteronism
|
|
Rx ascites
|
use aldosterone blocker (acidosis increases loss ammonium in stool)
|
|
Lab findings cirrhosis
|
decrease BUN, glucose, sodium, potassium, calcium (decrease vitamin D); increase PT
|
|
Liver cell adenoma
|
estrogen related (steroids, oral contraceptives); intraperitoneal hemorrhage
|
|
Liver cancer
|
metastasis MC cancer; lung cancer MC primary site
|
|
Cholangiocarcinoma
|
primary sclerosing cholangitis MCC, C.C sinensis
|
|
Pathogenesis of cholesterol stones
|
bile with too much cholesterol and too little bile salts
|
|
Gallbladder cancer risk factors
|
cholelithiasis and porcelain gallbladder
|
|
Sentinel loop
|
localized ileus of duodenum due to acute pancreatitis
|
|
Pancreatic pseudocyst
|
abdominal mass; persistence of increase serum amylase >1 week
|
|
First sign tubule cell dysfunction
|
inability to concentrate urine
|
|
Positive urine nitrite + positive urine leukocyte esterase
|
urinary tract infection
|
|
Bladder smooth muscle hypertrophy
|
prostate hyperplasia constricts urethra
|
|
Priapism
|
persistent/painful erection; HbSS
|
|
Squamous cell carcinoma penis
|
HPV and lack of circumcision most important risk factors
|
|
Epididymitis
|
<35 - N. gonorrhoeae, C. trachomatis; >35 - E. coli, P. aeruginosa
|
|
S/S Epididymitis
|
scrotal pain relieved by elevation of scrotum (Prehn's sign)
|
|
Torsion of testicle
|
testicle high in canal; absent cremasteric reflex
|
|
Risk factors Testicular cancer
|
cryptorchid testis, Klinefelter's, testicular feminization
|
|
Seminoma
|
MC cancer; radiosensitive; large cells with lymphoid infiltrate; small percentage have increased hCG
|
|
Spermatocytic variant
|
>65 yrs of age
|
|
Embryonal carcinoma in testis
|
hemorrhage/necrosis; hematogenous spread before lymphatic; increased AFP, hCG
|
|
Yolk sac tumor
|
MC testicular cancer in boys; increased AFP
|
|
Choriocarcinoma in testis
|
most aggressive testicle cancer; increased hCG
|
|
Teratoma in testis
|
more often benign in children than adult
|
|
Teratocarcinoma in testis
|
teratoma + embryonal carcinoma
|
|
Malignant lymphoma in testis
|
MC type in elderly; metastasis not primary cancer
|
|
Prostatitis
|
perineal pain, fever; WBCs at end of voiding
|
|
PSA
|
sensitive but not specific for prostate cancer; increase in hyperplasia
|
|
Kallmann's syndrome
|
absent GnRH, anosmia, absence of taste
|
|
Erection
|
parasympathetic response
|
|
Ejaculation
|
sympathetic response
|
|
Seminiferous tubule failure
|
increase FSH (decrease inhibin); decrease sperm count; normal LH and testosterone
|
|
Venous thrombus
|
fibrin clot with entrapped RBCs, WBCs, platelets; deep veins below knee (stasis)
|
|
Arterial thrombus
|
endothelial injury; platelets held together by fibrin
|
|
Fat embolus
|
long bone fractures; delayed symptoms (48 hrs); thrombocytopenia, hypoxemia
|
|
Amniotic fluid embolism
|
DIC; lanugo hair in maternal pulmonary arteries
|
|
Diving
|
1 atmosphere pressure increase with 33 foot descent into water; N2 gas dissolved in tissue
|
|
Kidneys
|
most susceptible organ in shock; straight portion proximal tubule most susceptible
|
|
Shock complications
|
ischemic ATN, multiorgan failure, increase AG metabolic acidosis
|
|
Transitional cell carcinoma
|
renal pelvis, ureter, bladder
|
|
Liposarcoma
|
MC sarcoma in adults
|
|
Embryonal rhabdomyosarcoma
|
MC sarcoma in children
|
|
Teratoma
|
ectoderm, endoderm, mesoderm derivatives; bone/teeth visible on x-ray
|
|
Hamartoma
|
normal tissue, normal site; bronchial hamartoma, Peutz Jeghers polyp
|
|
Choristoma
|
normal tissue aberrant tissue location; pancreatic tissue stomach wall
|
|
Mixed tumor
|
different morphologic patterns, same germ cell layer; pleomorphic adenoma parotid
|
|
Upregulate telomerase
|
increases telomere length; found in all neoplastic cells
|
|
E-Cadherin
|
intercellular adhesion; lose adhesion in malignant cells
|
|
Malignant cells
|
receptors for laminin (basement membrane), fibronectin (ECM)
|
|
Invasion enzyme
|
type IV collagenase (basement membrane)
|
|
Angiogenesis
|
basic fibroblast growth factor, vascular endothelium growth factor
|
|
Vessel invading carcinomas
|
renal cell carcinoma (renal vein, vena cava), hepatocellular carcinoma
|
|
Seeding
|
ovarian cancer, periphery lung, CNS via spinal fluid
|
|
Sites where metastasis more common primary cancer
|
lung, bone, brain, liver, adrenal
|
|
Sites where primary cancer more common than metastasis
|
GI tract, kidney, urogenital
|
|
Bone sites metastasis
|
vertebra MC (Batson venous plexus)
|
|
Osteoblastic metastasis
|
prostate cancer; increased serum AP, hypercalcemia
|
|
EM neurosecretory granules
|
carcinoid tumors, small cell carcinoma, neuroblastoma
|
|
EM thin and thick myofilaments
|
rhabdomyosarcoma
|
|
Cancers in children
|
leukemia (MC), CNS tumors, Burkitt's, Ewing's, neuroblastoma
|
|
Gynecologic cancers
|
endometrium > ovary > cervix
|
|
Malignant melanoma
|
fastest increasing in world
|
|
Southeast Asia (cancer)
|
hepatocellular carcinoma (HBV + aflatoxin)
|
|
Africa (cancer)
|
Burkitt's lymphoma, Kaposi sarcoma (HHV-8)
|
|
Parasitic causes of cancer
|
S. hematobium (SCC bladder), C. sinensis (cholangiocarcinoma)
|
|
Regulatory genes
|
proto-oncogenes, suppressor genes, anti-apoptosis genes
|
|
Overexpression
|
enhances activity of BCL-2
|
|
ERB-B2 POC
|
function growth factor receptor; activation bad prognostic sign for breast carcinoma
|
|
RAS POC
|
function-GTP signal transduction; point mutation; 30% of all human cancer
|
|
APC suppressor gene function
|
prevents nuclear transcription by catenin
|
|
Chromosome instability syndromes
|
AR; susceptibility to DNA damage; leukemias, lymphomas
|
|
Examples chromosome instability
|
Bloom syndrome, ataxia telangiectasia, Wiskott-Aldrich syndrome
|
|
Carcinogens
|
chemicals (MC), viruses, radiation, H. pylori, physical (squamous cancer in bum scar)
|
|
Polycyclic hydrocarbons
|
key chemical carcinogen (cigarette smoke)
|
|
Thorium dioxide
|
hepatocellular carcinoma, cholangiocarcinoma
|
|
Benzene
|
leukemia
|
|
EBV
|
Burkitt's; CNS lymphoma (AIDS); Hodgkin's mixed cellularity; nasopharyngeal carcinoma
|
|
UVB cancers
|
basal cell carcinoma, squamous cell carcinoma, malignant melanoma
|
|
Cachexia
|
due to tumor necrosis factor-α
|
|
Clubbing
|
possible marker for lung cancer
|
|
Non-bacterial thrombotic endocarditis mitral valve (cancer?)
|
possible marker for pancreatic cancer
|
|
AFP
|
hepatocellular carcinoma, yolk sac tumors
|
|
CEA
|
recurrence colorectal cancer
|
|
Renal cell carcinoma
|
EPO (polycythemia), PTH-related peptide (hypercalcemia)
|
|
Hepatocellular carcinoma
|
EPO (polycythemia), insulin-like factor (hypoglycemia)
|
|
Medullary carcinoma of thyroid
|
calcitonin (hypocalcemia), ACTH (ectopic Cushing's)
|
|
MCHC
|
average Hb concentration in RBCs; decrease in microcytic anemias; increase in spherocytosis
|
|
Thalassemias (MCV, RBC?)
|
decrease MCV, increase RBC count
|
|
RDW
|
RBC size variation; increase iron deficiency; normal in other microcytic anemias
|
|
Total iron binding capacity
|
increase iron deficiency; decrease anemia chronic disease, sideroblastic anemia
|
|
Fe % Saturation
|
decrease iron deficiency, anemia chronic disease; increase sideroblastic anemia
|
|
Serum ferritin
|
decrease iron deficiency; increase anemia chronic disease, sideroblastic anemia; normal thalassemia
|
|
Microcytic anemias
|
iron deficiency MC, anemic chronic disease, thalassemia, sideroblastic anemia
|
|
Iron deficiency child
|
MCC Meckel's diverticulum
|
|
Stages iron deficiency
|
decrease ferritin; decrease Fe and % saturation, increase TIBC; normocytic then microcytic anemia
|
|
Anemia chronic disease
|
MC anemia in malignancy and alcoholics
|
|
α-Thalassemia trait
|
AR; two α-globin gene deletions; normal Hb electrophoresis
|
|
HbH disease
|
three α-globin gene deletions; hemolytic anemia; four β-globin chains
|
|
Hb Bart's disease
|
four α-globin gene deletions; four γ-globin chains
|
|
β-Thalassemia minor
|
AR; DNA splicing defect; increase HbA2 and F; decrease HbA
|
|
β-Thalassemia major
|
nonsense mutation with stop codon; hemolytic anemia; increase HbF, increase HbA2
|
|
Sideroblastic anemia
|
defect in mitochondrial heme synthesis producing ringed sideroblasts
|
|
Causes sideroblastic anemia
|
alcohol, pyridoxine deficiency (isoniazid Rx of TB), Pb poisoning
|
|
Pb poisoning
|
inhibition ferrochelatase, d-aminolevulinic acid dehydrase, ribonuclease
|
|
S/S Pb poisoning adult
|
peripheral neuropathy; proximal renal tubule damage (Fanconi's syndrome)
|
|
Lab Pb poisoning
|
coarse basophilic stippling RBCs; decrease MCV; increase blood Pb; increase d-aminolevulinic acid
|
|
R factor
|
binds with B12 in mouth, removed by pancreatic enzymes in small intestine
|
|
Causes B12 deficiency
|
vegan, pernicious anemia MC, fish tapeworm, pancreatitis, bacterial overgrowth, Crohn's disease
|
|
Causes folate deficiency
|
alcohol MCC, poor diet, drugs, malabsorption, pregnancy, goat milk
|
|
Drugs and folate deficiency
|
alcohol, OC, phenytoin, methotrexate, trimethoprim, 5-fluorouracil
|
|
Intestinal conjugase in folate metabolism
|
inhibited by phenytoin
|
|
Jejunal uptake of monoglutamate form of folate
|
inhibited by alcohol and OC
|
|
Dihydrofolate reductase inhibited by
|
inhibited by methotrexate, trimethoprim
|
|
Thymidylate synthetase inhibited by
|
inhibited by 5-fluorouracil
|
|
Folate deficiency
|
MCC of increased serum homocysteine
|
|
Lab findings unique to B12 deficiency
|
increase gastrin (pernicious anemia), increase methylmalonic acid
|
|
Aplastic anemia
|
drugs (e.g., phenylbutazone); infection (e.g., parvovirus); benzene
|
|
Intravascular hemolysis
|
decrease serum haptoglobin; hemoglobinuria; hemosiderinuria
|
|
Congenital spherocytosis
|
AD; defect in spectrin; extravascular hemolysis; splenomegaly
|
|
Blood findings in spherocytosis
|
normocytic anemia; dense RBCs, increase MCHC, increase osmotic fragility
|
|
PNH
|
missing decay accelerating factor; complement destruction RBCs, neutrophils, platelets
|
|
S/S PNH
|
pancytopenia; hemoglobinuria; positive sugar water test and acidified serum test
|
|
Causes of sickling
|
increase deoxyhemoglobin (hypoxemia, acidosis); HbS > 60%
|
|
HbF
|
inhibits sickling; hydroxyurea increase HbF
|
|
HbSS children
|
dactylitis (6-9 months); Streptococcus pneumoniae sepsis (dysfunctional spleen)
|
|
HbSS complications
|
aplastic crisis (parvovirus B-19), acute chest syndrome, autosplenectomy, calcium bilirubinate gallstones, priapism, aseptic necrosis
|
|
HbAS
|
microhematuria from sickling in renal medulla; renal papillary necrosis
|
|
Hb electrophoresis
|
HbAS-HbA 55-60%, HbS 40-45%; HbSS-HbS 90-95%, HbF 5-10%
|
|
Blood findings in HbSS
|
sickle cells; target cells; Howell-Jolly bodies (nuclear remnants)
|
|
Warm type AIHA
|
IgG; extravascular hemolysis; e.g., SLE, drugs
|
|
Cold type AIHA
|
IgM intravascular hemolysis; e.g., CLL, Mycoplasma
|
|
Penicillin induced hemolysis
|
IgG antibody against penicillin attached to RBC (type II hypersensitivity)
|
|
Methyldopa induced hemolysis
|
drug alters Rh antigens; IgG antibody against Rh antigens (type II hypersensitivity)
|
|
Quinidine induced hemolysis
|
drug-IgM IC; intravascular hemolysis; type III hypersensitivity
|
|
Lab findings AIHA
|
positive direct Coombs'; spherocytes
|
|
Peripheral blood findings micro/macro hemolysis
|
schistocytes; iron deficiency from hemoglobinuria
|
|
Malaria
|
intravascular hemolysis correlates with fever; falciparum-ring forms and gametocytes
|
|
Leukoerythroblastic reaction
|
marrow infiltrative disease peripheralizes myeloblasts/nucleated RBCs
|
|
Causes of leukoerythroblastic reaction
|
bone metastasis MCC, myelofibrosis
|
|
Helminthes not producing eosinophilia
|
pinworms, adult worms in ascariasis
|
|
Atypical lymphocytes
|
mononucleosis; CMV; toxoplasmosis; viral hepatitis; phenytoin
|
|
Lab findings mono
|
atypical lymphocytosis; IgM heterophile antibodies against horse RBCs
|
|
Lymphopenia
|
T cell deficiencies (HIV); combined B/T deficiency (adenine deaminase deficiency)
|
|
Lymphocytosis
|
viral infections, whooping cough
|
|
Corticosteroids
|
lymphopenia, eosinopenia, neutrophilia
|
|
Chronic MPD
|
neoplastic stem cell disorder; splenomegaly; marrow fibrosis; risk for leukemia
|
|
Examples of MPD
|
polycythemia vera, myelofibrosis and myeloid metaplasia
|
|
Absolute polycythemia
|
increase RBC count and RBC mass
|
|
Appropriate polycythemia
|
hypoxic stimulus for EPO to generate RBCs
|
|
Appropriate absolute polycythemia
|
normal plasma volume; increase RBC mass; decrease SaO2; increase EPO
|
|
Polycythemia vera
|
increase plasma volume and RBC mass; normal SaO2; decrease EPO
|
|
Ectopic EPO (renal cell carcinoma)
|
normal plasma volume; increase RBC mass; normal SaO2; increase EPO
|
|
Myelofibrosis myeloid metaplasia
|
marrow fibrosis; extramedullary hematopoiesis; splenomegaly
|
|
Lab findings in myelofibrosis
|
tear drop RBCs; dry bone marrow aspirate (marrow fibrosis)
|
|
Essential thrombocythemia
|
MPO with increase in abnormal appearing platelets
|
|
Myelodysplastic syndrome
|
severe anemia in elderly; 30% develop leukemia; ringed sideroblasts
|
|
Acute vs. chronic leukemia
|
acute, blasts >30% in bone marrow; chronic, blasts <10% in bone marrow
|
|
Acute monocytic leukemia
|
gum infiltration
|
|
CML
|
t(9;22) of ABL POC; Philadelphia chromosome 22; decrease alkaline phosphatase score
|
|
ALL
|
early pre-B (80%); CALLA (CD10) and TdT positive; CNS and testicle involvement ; t(12;21) offers good prognosis
|
|
CLL
|
B cell neoplasm; decrease γ-globulins; MCC generalized lymphadenopathy patients> 60-yrs-old
|
|
Adult T cell leukemia
|
HTLV-1; CD4 T cells; skin infiltration; lytic bone lesions with hypercalcemia
|
|
Hairy cell leukemia
|
positive TRAP stain; splenomegaly; Rx with purine nucleosides
|
|
Nodal sites
|
germinal follicles, B cells; paracortex, T cells; sinuses, histiocytes
|
|
Phenytoin
|
atypical lymphocytosis
|
|
Cat scratch disease
|
Bartonella henselae; granulomatous microabscesses
|
|
Extra nodal lymphomas
|
risk factors H. pylori (stomach); Sjogren's syndrome
|
|
Mycosis fungoides
|
CD4 T cell neoplasm; skin lesions with Pautrier's microabscesses
|
|
Sezary syndrome
|
leukemic phase of mycosis fungoides
|
|
MGUS
|
MC monoclonal gammopathy; may progress to myeloma
|
|
Waldenstrom's macroglobulinemia
|
lymphoplasmacytic lymphoma; IgM M spike; hyperviscosity
|
|
Lymphocyte predominant Hodgkin's
|
infrequent classic RS cells
|
|
Nodular sclerosing Hodgkin's
|
female dominant; supraclavicular nodes + anterior mediastinal nodes
|
|
Mixed cellularity Hodgkin's
|
male dominant; numerous RS cells; EBV association
|
|
Alkylating agents in Rx of Hodgkins
|
increase risk for second malignancies (leukemia; NHL)
|
|
Langerhan's histiocytes
|
CD1 positive; Birbeck granules
|
|
Letterer-Siwe disease
|
malignant histiocytosis <2 yrs old; diffuse eczematous rash; organ involvement
|
|
Hand-Christian-Christian disease
|
malignant; lytic skull lesions, diabetes insipidus, exophthalmos
|
|
Eosinophilic granuloma
|
benign histiocytosis; lytic bone lesions with pathologic fractures
|
|
Urticaria pigmentosum
|
localized mastocytosis; skin lesions swell and itch with scratching
|
|
Amyloid
|
twisted β-sheet; apple green birefringence with Congo red
|
|
Primary amyloidosis
|
AL amyloid derived from light chains; plasma cell disorders
|
|
Secondary amyloidosis
|
AA amyloid derived from serum-associated amyloid; chronic infections
|
|
Alzheimer's disease
|
amyloid precursor protein gene product chromosome 21; amyloid-β
|
|
Heparin
|
enhances ATIII activity (neutralizes all factors except V, VIII, fibrinogen)
|
|
Procoagulants
|
coagulation factors, thromboxane A2 (platelet aggregation, vasoconstrictor)
|
|
Protein C and S
|
inactivate factors V and VIII; enhance fibrinolysis
|
|
Extrinsic system factor
|
VII
|
|
Intrinsic system factors
|
XII, XI, IX, VIII
|
|
Final common pathway factors
|
X, V, prothrombin (II), fibrinogen (I)
|
|
Factor XIII
|
cross-links insoluble fibrin; strengthens fibrin clots
|
|
Factors consumed in a clot
|
fibrinogen, prothrombin, V, VIII; fluid is called serum
|
|
Plasmin
|
cleaves fibrinogen and insoluble fibrin into degradation products
|
|
Tests for vWF
|
ristocetin cofactor assay; vWF antigen assay; agar electrophoresis
|
|
PT
|
evaluates extrinsic pathway to fibrin clot
|
|
PTT
|
evaluates intrinsic pathway to stable fibrin clot
|
|
Fibrinolysis tests
|
fibrin(ogen) degradation products; D-dimers (cross-linked insoluble fibrin)
|
|
Idiopathic thrombocytopenic purpura (ITP)
|
children; antibodies against GpIIb:IIIa; no splenomegaly
|
|
Chronic autoimmune thrombocytopenic purpura
|
SLE; antibodies against GpIIb:IIIa receptors
|
|
Heparin induced thrombocytopenia
|
thrombocytopenia due to IgG antibody against heparin attached to PF4 on platelets
|
|
PF4
|
heparin neutralizing factor
|
|
HIV
|
thrombocytopenia MC hematologic abnormality; similar to ITP
|
|
S/S TTP
|
fever, thrombocytopenia, renal failure, hemolytic anemia with schistocytes, CNS deficits
|
|
Lab findings TTP
|
thrombocytopenia, prolonged bleeding time, normal PT and PTT
|
|
HUS
|
similar to TTP; endothelial injury from Shiga-like toxin of 0157:H7 E. coli in undercooked beef
|
|
Desmopressin acetate
|
Rx of choice for mild von Willebrand's disease and hemophilia A
|
|
Antiphospholipid antibodies
|
lupus anticoagulant and anticardiolipin antibodies; vessel thrombosis
|
|
Factor V Leiden
|
MC hereditary thrombosis; resistant to degradation by protein C/S
|
|
Blood group O
|
some patients have anti-AB-IgG antibodies; increased incidence duodenal ulcers
|
|
Rh antigens
|
inherited in autosomal codominant fashion; Rh antigens include D, C, c, E, e
|
|
Atypical antibodies
|
antibodies against Rh or non-Rh blood group antigens (e.g., anti-D)
|
|
Duffy antigen
|
receptor for Plasmodium vivax; blacks often lack Duffy antigen
|
|
Antibody screen
|
indirect Coomb's test; detects atypical antibodies in serum
|
|
Cytomegalovirus
|
MC infection transmitted by blood transfusion; MC antibody
|
|
Hepatitis C
|
MCC of post-transfusion hepatitis
|
|
Major crossmatch
|
patient serum reacted against donor RBCs; does not guarantee RBC survival
|
|
Packed RBC transfusion
|
raises Hb by 1 gm/dL and Hct by 3%
|
|
Cryoprecipitate
|
fibrinogen and factor VIII
|
|
Allergic transfusion reaction
|
type I IgE-mediated hypersensitivity reaction
|
|
Febrile transfusion reaction
|
recipient anti-HLA antibodies react against donor leukocytes
|
|
Extravascular HTR
|
antibody attaches to donor RBCs; macrophage phagocytosis and hemolysis
|
|
Positive direct Coomb's test
|
present in both types of hemolytic transfusion reactions
|
|
ABO HDN
|
mother O and baby A or B; transplacental passage of maternal anti-AB-IgG; positive direct Coomb's test; spherocytes; MCC unconjugated hyperbilirubinemia first 24 hrs
|
|
Rh immune globulin
|
anti-D; coats D antigen site on fetal RBCs in maternal circulation
|
|
Rh HDN lab
|
positive direct Coomb's; severe anemia and hyperbilirubinemia
|
|
ABO HDN
|
protects mother from Rh sensitization (development of anti-D antibodies)
|
|
O Rh negative mother with A Rh positive baby
|
A+ cells destroyed by mothers anti A-lgM
|
|
Which is likely to present with systemic symptoms+large joint involvement,JRA or adult onset rheumatoid arthritis?
|
Juvenile rheumatoid arthritis
|
|
What is the surface antigen found on pluripotent stem cells?
|
CD34
|
|
What is the surface antigen found on APC's and what receptor does it bind on T lymphocytes?
|
B7 binds CD28 on helper T lymphocytes
|
|
What are the three vasculitides associated with antineutrophil cytoplasmic antibodies (ANCA)?
|
Microscopic polyangiitis, Wegener's granulomatosis and Churg-Strauss syndrome
|
|
Initial vessel events
|
transient vasoconstriction → arteriolar vasodilation → increase venular permeability
|
|
Neutrophil rolling acute inflammation
|
due to selectins
|
|
Integrins
|
neutrophil adhesion molecules; C5a and leukotriene B, activate; neutrophil margination
|
|
CD11/CD18
|
markers for integrins
|
|
Endothelial cell adhesion molecules
|
activated by IL-1 and TNF
|
|
Activation neutrophil adhesion molecules
|
neutrophilic leukocytosis; corticosteroids; neutropenia; endotoxins
|
|
Opsonizing agents
|
IgG, C3b; enhance phagocytosis
|
|
Neutrophils, monocytes, macrophages
|
receptors for IgG, C3b
|
|
Opsonization defect
|
Bruton's agammaglobulinemia (XR, decreased IgG)
|
|
Phagocytosis defect
|
Chediak-Higashi (see cell injury); also has defect in microtubule polymerization
|
|
PGE2
|
vasodilation, fever
|
|
Nitric oxide
|
vasodilator; FR gas from conversion arginine to citrulline
|
|
IL-1 and TNF
|
fever, synthesis acute phase reactants in liver, leukocytosis
|
|
IL-6
|
stimulated by IL-1; stimulates synthesis of acute phase reactants
|
|
Acute phase reactants
|
fibrinogen, ferritin, C-reactive protein
|
|
Bradykinin
|
kinin produced in conversion of factor XII to factor XI; pain, vasodilator, vessel permeability; cough/angioedema, ACE inhibitors
|
|
Anaphylatoxins
|
C3a and C5a; directly stimulate mast cell release of histamine
|
|
Zileuton
|
inhibits lipoxygenase
|
|
Zafirlukast, montelukast
|
block lipoxygenase receptor
|
|
TXA2
|
synthesized by platelets; platelet aggregation, vasoconstriction, bronchoconstriction
|
|
Dipyridamole
|
inhibits thromboxane synthase
|
|
Corticosteroids
|
inhibits phospholipase A2, activation neutrophil adhesion molecules; neutrophilic leukocytosis, lymphopenia, eosinopenia
|
|
This gram positive cocci is a common cause of nosocomial urinary tract infections and subacute endocarditis.
|
Enterococcus, treated with ampicillin
|
|
What is the treatment for chlamydia urethritis?
|
Azithromycin or doxycycline
|
|
Patient presents with recurrent pyogenic infections, pruritic papulovesicular dermititis, and thrombocytopenia.
|
Wiskott-Aldrich syndrome
|
|
What is the treatment for toxoplasmosis?
|
Sulfadiazine and pyrimethamine
|
|
8 yro boy presents with fever, sore throat, tonsillar exudates, tender anterior cervical lymph nodes. Etiologic agent?
|
Classic strep throat; Streptococcus pyogenes
|
|
Clinical methemoglobinemia
|
cyanosis not corrected by O2; chocolate colored blood
|
|
Increased A-a gradient
|
primary lung disease; left to right shunts in heart
|
|
Choanal atresia
|
cyanotic when breast feeding; turns pink when crying
|
|
Nasal polyps
|
allergic (MC; adults only), aspirin, cystic fibrosis
|
|
Nasal polyp in a child
|
requires sweat test to exclude cystic fibrosis
|
|
Triad asthma
|
patient on aspirin (pain syndrome) with nasal polyps, asthma
|
|
Sinusitis
|
maxillary sinusitis MC in adults; ethmoiditis MC in children; S. pneumoniae MC
|
|
Resorption atelectasis
|
MCC of fever 24-36 hours after surgery
|
|
Causes RDS
|
prematurity, maternal diabetes, C-section
|
|
Complications RDS
|
O2 FR injury (blindness, bronchopulmonary dysplasia); necrotizing enterocolitis
|
|
Rhinovirus
|
MCC common cold; hand to mouth transmission
|
|
Respiratory syncytial virus
|
MCC pneumonia and bronchiolitis in child
|
|
Parainfluenza virus
|
MCC croup in child; trachea area of obstruction
|
|
Cytomegalovirus
|
basophilic intranuclear inclusion surrounded by halo
|
|
Influenza
|
superimposed pneumonia with S. aureus increases mortality
|
|
Rubeola
|
Warthin-Finkeldey multinucleated giant cells
|
|
Chlamydia pneumoniae
|
atypical pneumonia; association with coronary artery disease
|
|
Chlamydia trachomatis
|
pneumonia in newborns; staccato cough; wheezing
|
|
Coxiella burnetii
|
only rickettsia without a vector
|
|
Staphylococcus aureus pneumonia
|
tension pneumatocysts in children with cystic fibrosis
|
|
Inspiratory stridor child
|
croup, epiglottitis
|
|
Pseudomonas aeruginosa
|
MCC of pneumonia and death in cystic fibrosis; green sputum
|
|
S/S Coccidioides immitis
|
erythema nodosum (painful nodules lower legs)
|
|
H. capsulatum
|
simulates TB; yeasts phagocytosed by macrophages
|
|
Mycobacterium avium intracellulare (MAI)
|
atypical TB; MC TB in AIDS
|
|
Aspiration sitting
|
posterobasal segment right lower lobe
|
|
Aspiration supine
|
superior segment right lower lobe
|
|
Aspiration right side
|
right middle lobe, posterior segment right upper lobe
|
|
ARDS
|
RLD; non-cardiogenic pulmonary edema due to alveolar injury; neutrophil destruction of type I and II pneumocytes; hyaline membranes
|
|
Causes of ARDS
|
septic shock (MC), aspiration gastric contents, severe trauma
|
|
Pneumoconiosis
|
inhalation mineral dust causing interstitial fibrosis; particles <0.5 μm to reach alveoli
|
|
Caplan syndrome
|
pneumoconiosis + rheumatoid nodules in lungs
|
|
Coal worker's
|
"black lung" disease; progressive massive fibrosis; no increased incidence cancer or TB
|
|
Silicosis
|
quartz; nodular opacities; foundry workers; increase incidence cancer and TB
|
|
Ferruginous bodies
|
asbestos fiber coated by iron
|
|
Kveim test
|
intradermal injection sarcoid antigens causes skin reaction
|
|
Farmer's lung
|
RLD; lung reaction against thermophilic bacteria in moldy hay
|
|
Silo filler's disease
|
RLD; reaction against nitrogen dioxide in fermenting corn
|
|
Byssinosis
|
RLD; reaction against cotton, linen, hemp products in textile industry
|
|
Collagen vascular RLD
|
SLE, rheumatoid arthritis, systemic sclerosis
|
|
Drugs RLD
|
amiodarone, bleomycin, busulfan, cyclophosphamide, methotrexate, nitrofurantoin
|
|
Obstructive lung disease
|
increase compliance, decrease elasticity; increase RV, TLC; decrease TV, VC; decrease FEV1sec and FVC; decrease FEV1sec/FVC ratio
|
|
Examples of Obstructive lung disease
|
asthma, emphysema, chronic bronchitis, bronchiectasis
|
|
Charcot-Leyden crystals
|
derive from crystalline material in eosinophil granules
|
|
Respiratory unit
|
respiratory bronchiole, alveolar duct, alveoli
|
|
Paraseptal emphysema
|
upper lobe destruction/distention alveolar ducts, alveoli; pneumothorax
|
|
Lab findings Emphysema
|
normal to decreased PCO2 (respiratory alkalosis)
|
|
Site of obstruction Chronic bronchitis
|
terminal bronchioles (proximal to respiratory unit)
|
|
Lab findings Chronic bronchitis
|
respiratory acidosis/hypoxemia
|
|
Causes Bronchiectasis
|
CF MCC, TB, immotile cilia syndrome
|
|
Squamous lung cancer
|
cavitate; secrete PTH-related protein
|
|
Bronchioloalveolar carcinoma
|
no smoking relationship; lung consolidation resembling pneumonia
|
|
Scar carcinoma of lung
|
usually adenocarcinoma developing in old TB scar
|
|
Bronchial carcinoid
|
low grade malignant; hemoptysis; rare cause carcinoid syndrome
|
|
Metastatic lung cancer
|
more common than primary cancer; breast cancer MCC
|
|
Solitary coin lesion
|
granuloma MCC
|
|
Anterior mediastinal masses
|
thymoma; nodular sclerosing Hodgkin's; teratomas
|
|
Posterior mediastinal masses
|
usually neurogenic tumors of ganglia
|
|
Myasthenia gravis
|
B cell hyperplasia of thymus MC abnormality; association with thymoma
|
|
Thymoma
|
association with hypogammaglobulinemia, autoimmune disease, pure RBC aplasia
|
|
Sterile pyuria
|
positive urine leukocyte esterase but negative standard culture; TB, C. trachomatis
|
|
Serum BUN:creatinine ratio
|
<15:1 (renal failure); >15:1 (prerenal or postrenal azotemia)
|
|
WBC casts
|
acute pyelonephritis, acute tubulointerstitial nephritis
|
|
Fatty casts with Maltese crosses
|
nephrotic syndrome
|
|
Cystinuria
|
hexagonal crystals
|
|
Renal dysplasia
|
MC childhood cystic disease; abnormal development; flank mass
|
|
Visceral epithelial cells
|
synthesize basement membrane
|
|
Glomerular BM
|
negative charge due to heparan sulfate
|
|
Focal segmental glomerulosclerosis
|
nephrotic syndrome; AIDS and IV heroin abuse
|
|
Causes membranous GN
|
HBV, ACE inhibitors, cancer
|
|
Type I MPGN
|
nephrotic; subepithelial deposits; HCV association; tram tracks
|
|
Type II MPGN
|
nephrotic; C3 nephritic factor; intramembranous ICs (dense deposit disease)
|
|
DM nodular glomerulosclerosis
|
microalbuminuria first sign
|
|
DM glomerulosclerosis
|
nodules with collagen in mesangium; hyaline arteriolosclerosis of arterioles
|
|
Ischemic ATN
|
prerenal azotemia MCC; renal tubular cell casts; BUN:creatinine ratio <15:1; disruption of BM in proximal tubule and thick ascending limb
|
|
Nephrotoxic ATN
|
aminoglycosides, IVP dye, Pb/mercury poisoning; proximal tubule dysfunction; intact BM
|
|
Chronic pyelonephritis
|
U-shaped scars overlying blunt calyces
|
|
S/S Drug-induced tubulointerstitial nephritis
|
type I/IV reaction; e.g., penicillin; ARF, fever, rash, eosinophilia, eosinophiluria, WBC casts
|
|
Analgesic nephropathy
|
aspirin plus acetaminophen; renal papillary necrosis; IVP with ring defect
|
|
Myeloma kidney
|
BJ protein produces foreign body reaction in tubules
|
|
S/S CRF
|
pericarditis, prolonged bleeding time, normocytic anemia, pathologic fractures
|
|
Benign nephrosclerosis
|
kidney of hypertension; shrunken kidneys due to hyaline arteriolosclerosis
|
|
Renal infarction
|
pale infarcts; hematuria; common in polyarteritis nodosa
|
|
Staghorn calculus
|
due to urease producing organisms (Proteus); alkaline urine pH; ammonia smell
|
|
Angiomyolipoma
|
hamartoma; associated with tuberous sclerosis
|
|
Renal cell carcinoma
|
smoking MCC; invasion renal vein/vena cava; lung, bone mets; yellow colored
|
|
S/S Renal cell carcinoma
|
flank mass, hematuria; ectopic hormones (EPO, PTH related peptide), left-sided varicocele
|
|
Wilm's tumor
|
hypertension, unilateral abdominal mass in child; aniridia/hemihypertrophy in AD types
|
|
Urine draining from umbilicus
|
persistent urachus
|
|
Retroperitoneal fibrosis
|
produces hydronephrosis
|
|
Bladder extrophy
|
abdominal wall defect + epispadias
|
|
Bladder diverticula
|
most commonly due to prostatic hyperplasia with urethral obstruction
|
|
Acute cystitis
|
E. coli; females > males; no fever, flank pain, or WBC casts
|
|
S/S Bladder transitional cell carcinoma
|
hematuria; hydronephrosis
|
|
Bladder adenocarcinoma
|
risk factors persistent urachus, extrophy
|
|
Type II collagen
|
early wound repair
|
|
Laminin
|
key basement membrane glycoprotein
|
|
Fibronectin
|
key interstitial matrix glycoprotein
|
|
Angiogenesis in repair
|
basic fibroblast growth factor, vascular endothelial growth factor
|
|
Key event in wound repair
|
granulation tissue formation; fibronectin responsible
|
|
Collagenases
|
zinc cofactor (metalloprotease); type III collagen replaced by type I collagen
|
|
Tensile strength of healed wound
|
80% original strength
|
|
Inhibition wound healing
|
infection (MCC S. aureus), zinc deficiency, DM
|
|
Keloid
|
excessive type III collagen; common in blacks
|
|
Pyogenic granuloma
|
exuberant granulation tissue; bleeds when touched
|
|
Antimuscarinic used in the treatment of diabetic urinary incontinence
|
Oxybutynin
|
|
Patient presents with swollen and painful toes, history of conjunctivitis, urethritis, and diarrhea. Diagnosis?
|
Reiter syndrome; diarrhea caused by c. jejuni
|
|
An infant develops septic shock with abdominal distention and tenderness. What is most likely seen at surgery?
|
Gangrene of the terminal ileum and ascending colon; Necrotizing enterocolitis
|
|
Microdeletion of 15q11.2 can result in this syndrome.
|
Prader-Willi syndrome or Angelmann syndrome
|
|
Esophagitis with punched-out ulcers on endoscopy are likely due to what condition?
|
Herpes simplex virus
|
|
What is the method of increased virulence of strep pyogenes to scarlet fever?
|
Lysogenic conversion, where a temperate phage DNA is inserted into bacterial chromosome to become a prophage.
|
|
bilateral degeneration of what nerve results in wasting of the anterior compartment of the lower limb, gait disturbances?
|
Deep peroneal nerve; Charcot-Marie-Tooth disease
|
|
What dictates the maximum velocity of muscle shortening?
|
ATPase activity of the muscle
|
|
Pregant infection with Toxoplasma gondii results in this abnormality
|
First trimester: necrotizing encephalitis; Second and third trimester: retinochoroiditis
|
|
Hydrops fetalis is associated with what fetal infection?
|
B19 Parvovirus
|
|
UTI that is leukocyte esterase positive with no reactivity for nitrite. What organism is to blame.
|
Enterococcus faecalis or staph saprophyticus;
|
|
Aneurysm of the superior cerebellar artery would have effect what cranial nerve?
|
CN III, arises from interpeduncular fossa of the midbrain and then passes between SCA and PCA lateral to basilar artery
|
|
What percentage of hydatidiform moles progress to choriocarcinoma?
|
2%; luckily there choriocarcinomas of placental orgin are highly responsive to chemotherapy
|
|
This antibacterial is used in the treatment of acne vulgaris and gonococcal infections.
|
Tetracycline
|
|
This cytokine produced by TH1 cells acts on macrophages to enhance microbicidal activities.
|
IFN-gamma
|
|
This cytokine is produced by leukocytes to inhibit viral replication.
|
IFN-alpha
|
|
This cytokine is produced by fibroblasts to inhibit viral replication.
|
IFN-beta
|
|
This cytokine is produced by macrophages and NK cells, cytotoxic to tumor cells, induces cytokine production.
|
TNF-alpha
|
|
What stain is used to visualize cryptococcus neoformans and histoplasma?
|
Silver stain for histo, india ink for crypto
|
|
Patient presents with hyperpyrexia, muscle rigidity, altered mental status. What is the syndrome and what drugs?
|
Neuroleptic malignant syndrome (NMS); commonly associated with antipsychotic medications, as well as the antidepressant fluphenazine
|
|
Patient presents with history of staph aureus, aspergillus, and salmonella infection. Diagnosis?
|
Chronic granulomatous disease; NADPH oxidase defeciency (Patients are also susceptible to Nocordia and Candida infections)
|
|
Patients are more susceptible to severe staphylococci and streptococci infections, and rarely make it to adulthood.
|
Chediak-Higashi syndrome; mutated LYST gene resulting in impaired degranulation of lysosomes; associated with albinism
|
|
What is Marcus Gunn pupil and what is it associated with?
|
paradoxical dilation on swinging light test (from normal to Marcus Gunn pupil) caused by absence of adequate light entering pupil
|
|
What pupillary abnormalities would be expected with increased intracranial pressure?
|
Fixed and dilated, accompanied by ptosis, caused by compression of CN III parasympathetic fibers
|
|
Fat, carbohydrate, and protein in the duodenum all stimulate the release of this hormone?
|
GIP; CCK is released in response to fat and protein, but not carbohydrates
|
|
G5P0 woman suffers from recurrent miscarriages in the first trimester, what is the most likely cause?
|
t(14,21) Robertsonian translocation; bicornuate uterus can also result in recurrent miscarriages but first trimester is indicative of Robertsonian translocation
|
|
What innervates the opponens policis? What innervates the adductor policis?
|
Opponens policis: Median nerve; Adductor policis: Ulnar nerve
|
|
This portion of the brain is concerned primarily with planning and fine-tuning of movements and balance.
|
The cerebellum; cerebellar vermis; Damage will result in truncal ataxia with a wide-based "drunken-sailor" gait.
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Absence of deep tendon reflexes, extensor plantar response are commonly found with damage to this area of the brain.
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Medulla
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In what type of patients would you expect to see an elevated gamma-glutamyl transpeptidase?
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Alcoholics
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What type of hepatitis is associated with polyarteritis nodosa?
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Hepatitis B (and C but not as much as B)
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This drug decreases TG's, increases HDL, decreases C-reactive protein, and decreases blood glucose.
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Thiazolidinediones; Used to treat metabolic syndrome.
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Trousseau's syndrome is associated with this underlying condition?
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Pancreatic carcinoma; Trousseau's syndrome is migratory thrombophlebitis
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In a deficiency caused by deficient purine salvage enzyme HPRT, what is the substance that accumulates?
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Lesch-Nyhan syndrome; monosodium urate
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This type of seizure is characterized by loss of postural muscle tone that only lasts a few seconds.
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Atonic seizure
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What are the tumor suppressor genes associated with the following chromosomes: 3p, 5q, 17p, 17q, 18q?
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3p: VHL; 5q: APC (colon); 17p: p53 (Li-Fraumeni syndrome); 17q: BRCA-1; 18q: pancreatic cancer
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This test, is preferred over India ink when testing for cryptococcus neoformans infection.
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Latex particle agglutination
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This deficiency is the most common urea cycle disorder and results in elevated glutamine and urine orotic acid.
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Ornithine transcarbamoylase (OTC) deficiency
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This cytokine instructs macrophages to become epitheliod and form multinucleated giant cells
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Interferon gamma; which makes them more apt to engulf and eliminate foreign antigens.
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What would be the treatment for a patient with acute pyelonephritis with bacteremia?
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Ampicillin and gentamicin; drugs like erythromycin and tetracycline are bacteriostatic antibiotics and are not recommended in a patient w/ severe infection
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This neurotransmitter is of primary importance for induction of REM sleep.
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Acetylcholine
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Atrophy of the anterior horn produces muscle weakness, hypotonia, loss of deep tendon reflexes, absent babinski
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Werdnig-Hoffman disease
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What metabolite is frequently found in the urine of patients with carcinoid syndrome?
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5-HIAA; Carcinoid tumors may secrete variety of GI peptides (gastrin, insulin, VIP, glucagon) as well as ACTH and calcitonin
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This MOA-I blocks serotonin and norepinephrine reuptake to reduce appetite and increase energy expenditure.
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Sibutramine
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In hereditary nonpolyposis colon cancer and hereditary endometrial cancer, what is the result of the mutation?
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Deficient mismatch repair; typically resulting in microsatellite instability
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What are the 3 locations of elastic fibers?
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Large arteries, vocal cords, and ligamenta flava (which connects the vertebrae)
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Locked-in syndrome is due to inhibition of descending corticospinal and corticobulbar fibers. Damage to what?
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Pons, blocks Basilar artery
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In down syndrome, what is the defective embryologic event that produces the endocardial cushion defect?
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Inadequate migration of neural crest cells
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Babesia is transmitted via ixodes tick as is this organism?
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Borrelia Burgderfori; Dermacentor tick transmits rickettsia
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This drug at toxic levels can cause supraventricular tachycardia.
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Digoxin; Adenosine is the treatment
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Serum sickness is a condition commonly caused by hypersensitivity to drugs. What is the treatment?
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Oral prednisone (for arthralgias and skin rash) and diphenhydramine (to alleviate urticaria)
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Black necrotic lymph nodes transmitted by arthropod.
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Buboes; seen in Yersinia pestis (plague) spread by fleabite
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What count # must the platelet count be reduced to before generalized bleeding disorder becomes apparent?
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15,000-20,000; normal is 150K to 450K
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O antigen of salmonella, erythrogenic exotoxins of S pyogenes, diptheria toxin and botulinum toxin are all what location?
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Lysogenic phage genome
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The only location of striated muscle not under voluntary control.
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Esophagus
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This drug is a non-selective competitive alpha-blocker that has largely supplanted more selective alpha-1 blockers.
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Phentolamine
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This term is used to define multiple, often seemingly unrelated, physical effects caused by a single genotype.
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Pleiotropy; example is multiple bone fractures and blue sclerae seen in osteogenesis imperfecta
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Monoclonal antibody directed against the IL-2 receptor.
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Daclizumab
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This virulence factor converts hydrogen peroxide to water and oxygen, allowing it to survive in phagolysosomes.
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Catalase
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What part of the colon is retroperitoneal?
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Ascending and descending colon; also most of the pancrease and the distal 2/3rds of the duodenum
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A diet high in these is what is believed to be responsible for the increased incidence in gastric adenocarcinoma
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Food preservatives
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What effect do restrictive lung disease have on pulmonary compliance?
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They will increase elastance and thus decrease compliance
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This apolipoprotein activates lipoprotein lipase.
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CII
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A patient deficient in the complement factors C6, C7, and C8 are at risk for recurrent meningitis from this organism.
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Neisseria
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What virus is associated with cutaneous and mucous-membrane plaque-like violaceous lesions?
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Kaposi sarcoma, associated with HHV 8
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This drug prevents the binding of aminoacyl-tRNA to ribosomes.
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Tetracycline
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This type of amyloid is seen in primary amyloidosis and most frequently deposits in the heart.
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Transthyretin
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This type of amyloid is associated with secondary amyloidosis and deposition occurs in kidney, spleen and liver.
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Serum Amyloid-associated protein (SAA)
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This type of amyloid is seen in primary amyloidosis with systemic deposition.
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Amyloid light chain (AL)
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This type of amyloid is seen with long-term hemodialysis with musculoskeletal deposition.
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Beta-2 microglobulin
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What type of hypersensitivity is an Arthus reaction?
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Immune complex (type III) involving antibody, antigen, and complement activation
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60 yro man presents with bacterial meningitis, what are the most likely agents?
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S pneumoniae, Listeria, N meningitidis
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What test is used to distinguish between heritable and sporadic retinoblastoma?
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PCR; in heritable cases, any cell in the body will show altered chromosome (deletion or translocation), in sporadic caases only the tumor will show mutation
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Patient has CN dysfunction with the exception of the ability to look up. Diagnosis?
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Pinealoma; compresses vertical gaze center in the tectum of the midbrain
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Where are the estrogen, progesterone, and HER2 EGF receptors located?
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Estrogen and progesterone are located in the nucleus, HER-2, a growth factor, likely has it's receptor on the cell membrane
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Bilateral bruits of the renal arteries with a beaded pattern on angiography. If surresected, what would be apparent?
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Fibromuscular dysplasia
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The median nerve is subject to entrapment neuropathy when it passes between the two heads of what muscle?
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Pronator teres
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What is angiostatin?
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anti-angiogenic factor expressed by tumors that tends to inhibit angiogenesis
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These cells in the semineferous tubule have very pale nucleus and darkly staining nucleoli.
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Sertoli cells, establish blood-testis barrier via tight junctions (note they do not protect the spermatogonia which lie directly on BM)
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A patient with truncus arteriosus will also have what cardiac abnormality?
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VSD
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Chronic poisoning with this substance causes CNS atrophy, gingivitis, gastritis, and renal tubular changes.
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Chronic mercury poisoning
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Patients with Lamber-Eaton syndrome have autoantibodies directed against what cellular components?
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voltage-gated calcium channels
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Proliferative synovitis with many lymphocytes, macrophages, and plasma cells. Diagnosis?
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Rheumatoid arthritis
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What nerves are responsible for adduction and extension of the thumb?
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Ulnar nerve (adductor pollicis); Radial nerve (extensor pollicis longus and brevis)
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Malignant mesenchymal tumor that develops in the pelvis, shoulders, or ribs which appears slightly basophilic on H&E.
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Chondrosarcoma
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Benign bone-forming tumor composed of well-differentiated bone trabeculae arranged haphazardly.
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Osteoid osteoma or osteoblastoma (larger and found in vertebrae)
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How does one distinguish postmortem clots from premortem clots?
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Premortem clots usually have lines of Zahn, red, cell-rich layers in a thrombus that appear dark, grossly, alternating with these lines are light layers
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What is the rate limiting step in catecholamine synthesis?
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tyrosine to L-dopa by tyrosine hydroxylase
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This enzyme converts norepinephrine to epinephrine.
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Phenylethanolamine N-methyltransferase (PNMT)
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Dwarfism is caused by impaired: cell signaling, fibrillin synthesis, or type I collagen
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Impaired cell signaling (Fibroblast growth factor receptor); impaired fibrillin is Marfan syndrome, and type I collagen mutation causes osteogenesis imperfecta
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62 yro woman with solid, yellow ovarian mass and endometrial carcinoma. What type of tumor is in the ovary?
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Granulosa cell tumor; estrogen producing (risk factor for endometrial carcinoma)
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What is the test for the most common cause of neonatal meningitis?
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CAMP test (Group B strep or Strep agalactiae); test produces and additional zone of beta hemolysis that appears in an arrowhead formation on blood agar
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Volume distribution of a drug is 40L and the clearance is 2 L/hour, what is the halflife?
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t1/2=(0.7*Vd)/Cl; 14 hours
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Pertussis, in addition to inhibition of G protein complex, has this effect producing hypoglycemia
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Activates pancreatic islets of langerhans
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4 yro retarded child presents with a marfenoid-like appearance, what substance would be elevated?
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Homocysteineuria; Homocysteine or methionine (remethylated homocysteine via salvage pathway); like marfan but add mental retardation
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A patient with HIV presents with prolonged diarrhea, what is the likely causative agent?
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Mycobacterium avium or cryptosporidium parvum; crypto is more common but word association "prlonged diarrhea" matches for myco
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Syndrome is acute postviral injury damaging multiple systems but most notable for fatty liver with encephalopathy.
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Reye syndrome; most commonly caused by VZV and influenza A and B
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Thrombocytopenia, eczema, and recurrent sinopulmonary infections?
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Wiskott-Aldrich syndrome; Serum IgM low, but IgG, IgA, and IgE are all increased
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|
What is prosopagnosia?
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Damage of the visual association cortex resulting in the inability to recognize faces.
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|
What is Alexia?
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Inability to read caused by deficits in central language processing
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What is Anosognosia?
|
Deficit in cognition about one's illness, or lack of awareness that one is suffering from a certain condition
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|
Which is associated with production of prostaglandins important in renal blood flow, clotting, and GI protection?
|
COX-1; COX-2 is involved with prostaglandins for pain and inflammation, Celecoxib is a COX-2 inhibitor, Naproxen is a nonspecific COX inhibitor
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|
Translocation for mantle cell, multiple myeloma, and small cell?
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t(11,14)
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|
Lateral expansion of a pituitary tumor will effect what cranial nerve?
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Abducens nerve; leads to lateral rectus palsy, if it expands upward than optic nerve will be effected
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Trisomy fetus is spontaneously aborted, what is the most likely karyotype: 8, 13, 16, 18, or 21?
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16 is completely incompatible with life; 8 is also a common cause, but rare mosaics do survive, 13 is Pautau, 18 is Edwards, and 21 is Down syndrome
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|
What drug other than misoprostol can be used to keep the ductus arteriosus open.
|
Alprostadil a prostaglandin E1
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|
Mentally retarded child with seizures demonstrates leptomeningeal angiomatosis, nevus flammeus, and glaucoma.
|
Sturge-Weber syndrome (arteriovenous malformation); Nevus flammeus is port wine stain often of the face
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|
What cardiac abnormality is associated with fragile X syndrome?
|
Mitral valve prolapse and aortic root dilatation
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|
These drugs cause tachycardia and dry mouth (xerostomia).
|
Anticholinergic medications, such as amitriptyline (tricyclic antidepressant) used to treat clinical depression
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|
What is Naproxen?
|
and NSAID for mild to moderate pain
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|
Basophilic rhomboid crystals in a painful, swollen, and red joint. Diagnosis?
|
Pseudogout; calcium pyrophosphate crystals (If you can't remember gout or pseudogout, remember pseudogout hits the larger joints!)
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|
What drugs are associated with hypersensitivity myocarditis?
|
Antihypertensive agents, antibiotics, and diuretics
|
|
What percent of ingested salt is secreted by the kidneys?
|
95% the other 5% by the sweat glands
|
|
Gram negative diplococcus that is oxidase positive.
|
N gonorrhoeae
|
|
Patients with rheumatoid arthritis and sulfa allergies should avoid what drug?
|
Celecoxib, a NSAID that is a selective COX-2 inhibitor with a sulfa component
|
|
What test would be appropriate when candida albicans infection is suspected?
|
Germ tube test with pseudohypha formation in animal serum
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|
What is the Weil-Felix reaction?
|
anti-rickettsial antibody positive for typhus, rocky mountain spotted fever and crossreactive with proteus antigen
|
|
Patient with malaria with recalcitrant psoriasis. What is the treatment?
|
Atovaquone/proguanil; chloroquine, the drug of choice can worsen psoriasis (plaques on the skin and arthritic joints)
|
|
What layer is more superficial, camper fascia or scarpa fascia?
|
Camper fascia which is fatty is more superficial than the fibrous scarpa fascia
|
|
CD16 is the surface marker for what lymphocyte?
|
NK cells
|
|
What is absent in bare lymphocyte syndrome?
|
MHC class II necessary for APC presentation of peptides to T-helper cells; failure of CD4 helper cells education
|
|
These WBC's predominate in allergic responses.
|
Basophils and Eosinophils
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|
These structures cover most microvilli and apparently help protect these fragile structures from trauma.
|
Glycocalyx
|
|
Microtubule-dependent ATPase that helps drive transport along microtubules.
|
Kinesin
|
|
What diseases use ticks as a vector?
|
Borrellia Burgderfori, Babesia, Ricktsiae (Rocky mountain spotted fever), and Francisella tularensis
|
|
What nerve exits the greater sciatic foramen above the piriformis and what muscles does it innervate?
|
Superior gluteal nerve; innervates gluteus medius, gluteus minimus, and tensor fasciae latae
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|
The obturator nerve exits through the obturator canal and supplies these muscles.
|
Medial compartment; adductor longus, adductor brevis, part of adductor magnus and the gracilis
|
|
What nerve exits the greater sciatic foramen then passes through the elesser sciatic foramen?
|
Pudendal nerve
|