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241 Cards in this Set
- Front
- Back
Which embryonic structure becomes the ascending aorta and pulomary trunk?
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Truncus arteriosus
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Which embryonic structure becomes the right ventricle and smooth parts of left and right ventricle?
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Bulbus Cordis
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Which embryonic structure becomes a portion of the left ventricle?
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Primitive Ventricle
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Which embryonic structure becomes the coronary sinus?
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The left horn of the sinus venosus.
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Which embryonic structure becomes the SVC?
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Right common cardinal vein and right anterior cardinal vein.
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Causes urine discharge from the umbilicus:
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Patent Urachus
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Causes meconium discharge from the umbilicus or meckels diverticulum:
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Vitelline Fistula
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This tissue gives rise to the brain, the retina and the spinal cord:
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Neuroectoderm
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This tissue gives rise to the ANS, the dorsal root ganglia, cranial nerves, melanocytes, bones of the skull, schwann cells, etc.
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Neural Crest
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This tissue gives rise to gut tube epithelium and derivatives.
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Endoderm
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This tissue gives rise to the adenohypophysis, lens of the eye, epithelium of the oral cavity, sensory organs of the ear and olfactory epithelium.
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Surface ectoderm
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A craniopharyngioma is derived from:
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Surface Ectoderm
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Caused by excessive resorption of the septum primum or secundum:
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Patent foramen Ovale
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Drug that would help to close a PDA:
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Indomethacin
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Would help to maintain a PDA in a newborn:
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Prostaglandins
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Cerebellar tonsillar herniation through the foramen magnum with aqueductal stenosis and hydrocephaly. Often presents with syringomyelia and thoracolumbar myelomeningocele.
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Chiari II
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Large posterior fossa of the brian, absent cerebellar vermis with cystic enlargement of the 4th ventricle. Can lead to hydrocephalus and spina bifida.
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Dandy Walker
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Enlargement of the central canal of the spinal cord that leads to cape like bilateral loss of pain and temperature in the upper extremities with preservation of touch. Which fibers are typically damaged first?
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Syringomyelia- crossing fibers of the spinothalamic tract. Associated with Chiari II.
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This leads to a branchial cleft cyst in the lateral neck:
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Persistent cervical sinus
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Mullerian Inhibitory factor from _______ suppresses development of paramesonephric ducts.
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Sertoli Cells
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Increased androgens from _________ stimulates the development of mesonephric ducts
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Leydig cells
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Grown on Chocolate agar with factors V (NAD) and X (hematin).
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H. Influenzae
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Form on Thayer Martin or VPN media:
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N. Gonorrhoeae
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Grown on Tellurite plate or Loffler's media:
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C. diptheriae
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Grown on Eaton's agar:
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M. pneumoniae
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Grows on EMB agar as blue/black colonies with a metallic sheen:
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E. Coli
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Grows on Sabouraud's Agar
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Fungi
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This aerobe is seen in burn wounds, nosocomial pneumonia, and pneumonia in CF patients:
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Pseudomonas auruginosa
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Name three obligate anaerobes
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Clostridium, Bacteroides, and Actinomyces
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Name two intracellular bugs- must be in another cell because they can't make their own ATP:
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Chlamydia and Rickettsia
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This bacteria has a blue green pigment and smells like grapes:
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Psuedomonas Aeruginosa
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This bacteria have yellow sulfur granules that are composed of a mass of filaments and formed in pus
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Actinomyces Israelii
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This is the virulence factor of staph aureus- it binds to the Fc region of Ig and prevents opsonization and phagocytosis
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Protein A
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Is the virulence factor of S. pneumo, HiB, and Neisseria.
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IgA protease- helps to colonize respiratory mucosa
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This is the virulence factor of Group A strep: helps prevent phagocytosis
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M protein
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What mechanism causes the voluminous watery diarrhea of cholera?
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ADP ribosylation of G protein that stimulates adenylyl cyclse - increases NaCl in the gut
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Which bacteria produce toxins that stiumlate adenylate or guanylate cyclase?
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E. Coli
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This bacteria increases cAMP by inhibiting G-alpha
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B. pertussis
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This bacteria blocks the release of inhibitory neurotransmitters GABA and glycine
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C. tetani
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Bacteria that produces a toxin the cleaves host cell rRNA (inactivates 60s) and enhances cytokine release, causing HUS
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Shigella or EHEC
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Toxin that permanantly diables Gi
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Pertussis Toxin
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This toxin permanently activates Gs increasing cAMP.
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Vibrio cholerae
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This lancet shaped gram positive bacteria causes meningitis, otitis media, pneumonia, and sinusitis
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S. Pneumoniae
|
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This normal flora of the oral cavity causes dental carries and is resistant to optochin:
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S. viridans
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This bacteria is associated with rusty sputum, causes sepsis in sickle cell and ppl with splenectomy:
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S. pneumoniae
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Bacteria that can cause bacteremia and subacute endocarditis in colon cancer pts:
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Strep bovis
|
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The only bacteria with a polypeptide capsule:
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Bacillus anthracis
|
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Is a facultative intracellular bacteria with characteristic tumbling motility
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listeria
|
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Gram positive rod, anaerobe, causes oral/facial abcesses that drain through sinus tracts in skin.
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Actinomyces
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Gram postive and weakly acid fast aerobe that forms long, branching filaments and causes pulmonary infection in immunocompromised
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Nocardia asteroides
|
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How do you treat actinomyces?
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Penicillin
|
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How do you treat nocardia?
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Sulfa
|
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What is prophylaxis for exposure to TB?
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Azithromycin
|
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How do you treat leprosy?
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Long term oral dapsone
|
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This type of Neisseria ferments both maltose and glucose and has a capsule
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N. Meningococci- rifampin is prophylaxis in close contacts
|
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This gram negative bacteria causes epiglottitis, meningitis, otitis media, and pneumonia. How should you treat the meningitis?
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H. Influenza
Treat meningitis with ceftriaxone |
|
How do you treat legionella?
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Erythromycin
|
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This bacteria have flagella and disseminate hematogenously. They produce H2S
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Salmonella
|
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How do shigella move?
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actin polymerization
|
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This comma shaped or S shaped bacteria causes bloody diarrhea and is associated with Guillain Barre
|
Campylobacter jejuni
|
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This causes diarrhea that can mimic appendicitis. Transmission occurs through pets, contaminated milk or pork
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Yersinia enterocolitica
|
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Question mark shaped bacteria (spirochete) found in water contaminated with animal urine.
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Leptospira
|
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How do you treat Lyme dz?
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Doxycycline and ceftriaxone
|
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Is the only rickettsiae that is transmitted by aerosol and causes pneumonia:
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Coxiella (Q fever) - no rash, no vecor and a negative Weil Felix
|
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In the Weil-felix reaciton, Rickettsia cross reacts with ________ and agglutinates.
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Proteus O antigens
|
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Threeinfections that cause rash on the palms and soles:
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Coxsackie A, Syphilis and RMS
|
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How do you treat chlymidia:
|
Azithromycin or Doxy
|
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Is found in bird or bat droppings, endemic to the Mississippi and Ohio river valleys, and enters macrophages
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Histoplasmosis
|
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Found in states east of the Mississippi, causes inflammatory lung disease that can disseminate to skin and bone. Forms granulomatous nodules.
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Blastomycosis
|
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Found in the SW US, causes penumonia and meningitis, is associated with dust and has sperules filled with endospores
|
Coccidiomycoses
|
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Heavily encapsulated yeast found in pigeon droppings and soil. Is cultured on Sabourauds agar and confirmed by latex agglutination test.
|
Crytococcus Neoformans
|
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A mold with irregular non-septate hyphae found in diabetics with DKA or leukemia patients. They grow in the blood vessel and penetrate the cribiform plate- causes frontal lobe abcesses.
|
Mucor and Rhizopus
|
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Causes classic triad of chorioretinitis, hydrocephalus, and intracranal calcifications.
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Toxoplasma
|
|
Leishmaniasis causes spikning fevers, hepatomegaly and pancytopenia. How do you treat it?
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Sodium Stibogluconate
|
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Which are the live viruses?
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Smallpox, yellow fever, chickenpox (VZV), Sabin's polio, and MMR
|
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Which are the killed viruses?
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Rabies, Influenza, Salk Polio, and HAV
(RIP Always) |
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Which are the two recombinant virus vaccines?
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HBV and HPV
|
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The only DNA virus that is not double stranded:
|
Parvovirus
|
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Two RNA viruses that aren't single stranded
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Reo and Rotavirus
|
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Which DNA virus doesn't replicate in the nucleus?
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Pox
|
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Which two RNA viruses don't replicate in the cytoplasm?
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Influenza and Retro
|
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Which virus gets its envelope from the nuclear membrane?
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Herpes
|
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What are the seven DNA viruses?
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Herpes, Hepadna (HBV), Adeno, Parvo, Papilloma, Polyoma, and Pox
|
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High fevers for several days that can causes seizures followed by a diffuse macular rash
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Roseola- caused by HHV-6
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The number one causes of fatal diarrhea in children
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Rotavirus
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What type of virus is rubella?
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Toga virus
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Polio, Echo, Rhino, Cosackie and hepatitis A are all which kind of virus
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Picornavirus - all are fecal oral except rhino
|
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Influenza is which kind of virus?
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Orthomyxo- killed viral vaccine si major mode of protection
|
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Characterized by fever, postauricular tenderness, lymphadenopathy, arthralgias, and a fine trucal rash.
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Rubella- a toga virus
|
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Parainfluenza (croup), Mumps, measels and RSV are all which kind of virus?
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Paramyxovirus - has surface F protein that causes epithelial cells to join and become mutinucleated cells
|
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Illness characterized by cough, coryza, and conjunctivitis. Can cause SSPE years later, encephalitis, and giant cell pneumonia. Rash presents last and spreads form head to toe
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Rubeola (measels)- a paramyxovirus
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Causes parotitis, orchitis, and meningits- can cause sterility
|
Mumps- a paramyxovirus
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What are the three leading causes of UTI?
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E. Coli, S. Saptophyticus, Klebsiella
|
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Bacteria that causes swarming on Agar, produces protease, and is associated with struvite stones
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Proteus
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Congenital infection that causes cataracts and deafness with blueberry muffin rash:
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Rubella
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Congenital infection causing hearing loss and seizures with a petichial rash
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CMV
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This virus can causes hydrops fetalis if contracted in the 2nd or 3rd trimester- it is a ssDNA:
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Parvovirus B19
|
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Causes a vesicular rash on palms and soles with ulcers in the oral mucosa
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Hand Foot and Mouth Disease- Caused by Cosackie A
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Causes a positive PAS stain
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Tropheryma Whippeli
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Results from Dog or Cat bite
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Pasteurella Multocida
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Mutations of ________ are gain of function mutations leading to cancer. Need damage to only one allele:
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Oncogenes
|
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This gene codes for a tyrosine kinase and is mutated in CML:
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abl
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This gene codes for transcription factor and is mutated in Burkitt's lymphoma:
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c-myc
|
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This gene codes for an Anti-apoptotic molecule and is mutated in follicular and undifferentiated lymphomas
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bcl-2
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This gene codes for tyrosine kinase and is mutated in breast, ovarian, and gastric carcinomas:
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erb-2
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This gene codes for GTPase and is mutated in colon cancer:
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ras
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This gene codes for transcription factor and is mutated in lung cancer:
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L-myc
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This gene codes for transcription factor and is mutated in neuroblastomas
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N-myc
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This gene codes for tyrosine kinase and is mutated in MEN types II and III:
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ret
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This gene codes for cytokine receptor and is mutated in gastrointestinal stromal tumors (GIST)
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c-kit
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Mutation of these types of genes caues loss of function leading to cancer. Both alleles must be lost for expression of disease:
|
Tumor supressor genes
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This gene product blocks the G1-S phase of the cell cycle and mutation leads to retinoblastoma and osteosarcoma:
|
Rb (13q)
|
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This gene product blocks G1-S phase of the cell cycle and mutation is found in most cancers; Li-Fraumeni syndrome
|
p53 (17p)
|
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This gene codes for DNA repair protein and is indicated in breast and ovarian cancer:
|
BRACA1 (17q)
|
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This gene codes for a DNA repair protein and is mutated in breast cancer:
|
BRACA2 (13q)
|
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Which gene is mutated in melanoma?
|
p16
|
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Which gene is mutated in colorectal cancer associated with FAP?
|
APC
|
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Which tumor supressor gene is mutated in Wilm's tumor?
|
WT1
|
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Which tumor supressor gene is deleted in pancreatic cancer?
|
DPC
|
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Which tumor supressor gene is mutated in colon cancer?
|
DCC
|
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Used to screen for prostate cancer but can be elevated in BPH and prostatitis:
|
PSA
|
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Which marker is produced by most colorectal and pancreatic cancers and also produced by gastic, breast and thyroid medullary cancers?
|
CEA
|
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This tumor marker is elevated in hepatocellular carcinoma and yolk sac tumors in the testes?
|
Alpha fetoprotein
|
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This tumor marker is elevated in hydatidform moles, choriocarcinomas and gestational trophoblastic tumors:
|
beta HCG
|
|
This tumor marker is elevated in ovarian and malignant epithelial tumors:
|
CA-125
|
|
Tumor marker elevated in melanoma, neural tumors, and astrocytomas
|
S-100
|
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Is elevated in metastases to bone, obstructive biliary disease, and Paget's disease of the bone
|
Alk Phos
|
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Tumor marker for neuroblastoma, lung cancer and gastric cancer
|
Bombesin
|
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Tumor marker for hairy cell leukemia
|
TRAP
|
|
Tumor marker for pancreatic adenocarcinoma
|
CA 19-9
|
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Naphthlalene or aniline dyes cause which kind of cancer:
|
Bladder transitional cell carcinoma
|
|
Arsenic causes which kinds of cancer
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Squamous cell in skin and angiosarcoma in the liver
|
|
Which four cancers have psammoma bodies?
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Papillary thyroid, Serous ovary, meningioma, and mesothelioma
|
|
Top three cancers that mets to brain
|
Lung, Skin and Kidney
|
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Top three cancers that mets to the kidney
|
colon, stomach and pancreas
|
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Top three cancers that mets to bone:
|
Prostate, thyroid, and testes
|
|
Nicotinic ACh receptors are which kind of channels?
|
ligand gated Na+/K+
|
|
Muscarinic ACh receptors are which kind of channels?
|
G-protein coupled
|
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Which G protein pathway decreases adenylyl cyclase, decreasing cAMP, which decreases protein kinase A?
|
Gi = inhibitory pathway
|
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Which receptors use the G inhibitory pathway?
|
M2, A2, and D2
|
|
Which G protein pathway increases adenylyl cyclase, increasing cAMP and increasing protein kinase A?
|
Gs = stimulatory
|
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Which receptors use the Gs pathway?
|
B1, B2, D1, H2, V2
|
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Which G protein pathway acts through phospholipase C, increasing the conversion of lipids to PIP, producing IP3 and DAG, which cause an increase in intracellular calcium and protein kinase C?
|
Gq
|
|
Which receptors act through the Gq pathway?
|
H1, A1, V1, M1, M3
HAVe 1 M&M |
|
Drug used in the challenge test for asthma:
|
Methacholine - stimulates muscarinic receptors causing bronchoconstriction
|
|
Which anticholinesterase is used in the case of an atropine OD?
|
Physostigmine- crosses the blood brain barrier
Also used for glaucoma |
|
Used in cholinergic crisis involving glaucoma:
|
echothiophate
|
|
This muscarinic antagonist is used for asthma and COPD
|
Ipratropium
|
|
This drug is an equal B1 and B2 agonist
|
Isoproterenol
|
|
This drug is used as an alpha blocker before removing pheochromocytoma
|
Phenoxybenzamine
|
|
Three alpha 1 blockers used for HTN and urinary retention in BPH. Can cause orthostatic hypotension.
|
Prazosin, terazosin, and doxazosin (alpha1 blockers have zosin endings)
|
|
How do you treat a theophylline OD?
|
beta blocker
|
|
How do you treat poisoning with copper, arsenic or gold?
|
penicillamine
|
|
How do you treat an OD with tPA or streptokinase?
|
Aminocaproic Acid
|
|
Toxic doses of which two drugs are treated with NaHCO3 (alkylinization of the urine)?
|
Salicylates and TCAs
|
|
How do you treat beta blocker toxicity?
|
Glucagon
|
|
Name four non-selective beta blockers
|
propranolol, timolol, nadolol, and pindolol
|
|
Name the 5 B1 selective blockers
|
Acebutolol, Betaxolol, Esmolol, Atenolol and Metropolol
(A BEAM) |
|
Name two non-selective alpha and beta agonists:
|
Carvedilol and Labetalol
|
|
What do furosemide, probenecid, thiazides, and acetazolamide have in common?
|
They are sulfa drugs that can cause sulfa allergies in Pts.
|
|
This drug can cause a direct coombs positive hemolytic anemia:
|
Methyldopa
|
|
Which three drugs can cause pulmonary fibrosis?
|
Bleomycin, amidodarone, and Busulfan
|
|
Which durgs causes torsades de pointes?
|
Class III (sotalol) and class IA (quinidine) antiarrythmics
|
|
Name 4 P-450 inducers (cause decreased levels of other drugs):
|
Barbituates, SJW, Phenytoin and Rifampin
|
|
Name 4 P-450 inhibitors (increases the concentration of other drugs)
|
Erythromycin, Isoniazid, Ketoconazole, and Cimetidine
|
|
Adrenal insufficiency causing decreased sex hormones and cortisol but increased mineralocorticoids. Males have no internal sex organs and females never get mature sex characteristics. Causes hypertension and hypokalemia.
|
17-a hydroxylase
|
|
This adrenal insufficiency causes masculinization and hypertension. Increased levels of sexhormones but decreased aldosterone and cortisol.
|
11-B hydroxylase deficiency
|
|
Which adrenal insufficiency has decreased cortisol, decreased mineralocorticoids, and increased sex hormones. Leads to masculinization and hypotension.
|
21-hydroxylase deficiency
|
|
Characterized by parathyroid tumors, pituitary tumors (prolactin or GH) and pancreatic endocrine tumors (Zollinger Ellison, VIPomas). Commonly presents with kidney stones and stomach ulcers.
|
MEN 1
|
|
Characterized by medullary thyroid cancer (calcitonin), pheochromocytoma, and parathyroid tumors.
|
MEN II
|
|
Characterized by medullary thyroid cancer, pheochromocytoma and marfanoid habitus
|
MEN IIb or MEN III
|
|
Associated with antibodies to tissue transglutaminase, blunting of villi, and lymphocytes in the lamina propria. Associated with dermatitis herpetiformis
|
Celiac Sprue
|
|
Gastric hypertrophy with protein loss, parietal cell atrophy, and increased mucous cells. Precancerous. Rugae of the stomach become so hypertrophied that they look like brain gyri:
|
Menetrier's Dz
|
|
Autosomal dominant mutation of APC gene on chromosome 5. Has thousands of polyps and 100% progress to cancer:
|
FAP
|
|
Autosomal dominant mutation in DNA mismatch repair gene leading to colon cancer in 80% of cases:
|
HNPCC
|
|
Condition with FAP and malignant CNS tumor:
|
Turcot's syndromr
|
|
Condition with FAP and osseous soft tissue tumors, retinal hyperplasia
|
Gardner's Syndrome
|
|
In the progression to colon cancer, what is the order of gene mutations?
|
Loss of APC
K-RAS Loss of P53 |
|
Condition with mildly decreased UDP-glucuronyl transferase or decreased bilirubin uptake. Elevated unconjugated bilirubin without hemolysis. Caused by stress and has no clinical consequences.
|
Gilbert's Syndrome
|
|
Condition with absent UDP glucuronyl transferase. Patients have jaundice and kernicterus due to increased bilirubin. Pts die within a few years.
|
Crigler-Najjar
|
|
Conjugated hyperbilirubinemia due to defective liver excretion. Grossly black liver, benign.
|
Dubin Johnson
|
|
How do you treat wilson's dz?
|
Penacillamine
|
|
Cancer that has increased CEA and CA 19-9 tumor markers. Associated with smoking but not alcohol. Presents with abd pain radiating to the back, migratory thrombophlebitis, and obstructive jaundice.
|
Pancreatic adenocarcinoma
|
|
Drug that is a PGE1 analog and increases production/secretion of mucous, decreases acid.
|
Misoprostol
|
|
This somatostatin analog is used to treat VIPomas, carcinoid tumors, and acute variceal bleeds.
|
Octreotide
|
|
Monoclonal antibody to TNF- immune suppressant because TNF is a proinflammatory cytokine
|
Infliximab
|
|
Serotonin antagonist and powerful central acting anti-emetic
|
Ondansetron
|
|
This D2 receptor antagonist increases the resting tone of the stomach and increases motility. Used to treat gastroparesis:
|
Metoclopramide
|
|
Causes destruction of white matter of cervical region, random and assymetric lesions due to demyelination
|
Multiple Sclerosis
|
|
Combined upper and lower motor neuron deficits with no sensory deficit.
|
ALS
|
|
Complete occlusion of this artery in the spine spares the dorsal columns.
|
Anterior Spinal
|
|
Causes degeneration of dorsal roots and dorsal columns leading to impaired proprioception and locomotor ataxia
|
Tabes Dorsalis (syphilis)
|
|
Damages anterior white commissure of the spinothalamic tract resulting in bilateral loss of pain and temperature.
|
Syringomyelia
|
|
Which three conditions cause demyelination of dorsal columns, lateral corticospinal tracts, and spinocerebellar tracts leading to ataxic gait, hyperreflexia, impaired position and vibration
|
Vitamin B12 deficiency, Vitamin E deficiency, and Friedrich's ataxia
|
|
Autosomal recessive dz associtated with degeneration of anterior horns of the spinal cord with LMN involvement only. Presents as a floppy baby with tongue fasiculations. Die at 7 Months.
|
Werdnig Hoffman Disease- Spinal Muscular Atrophy
|
|
Autosomal recessive trinucleotide repeat disorder that leads to impaired mitochondrial functioning. Staggering gait, falls, nystagmus, dysarthria and hypertrophic cardiomyopathy. Presents in childhood with kyphoscoliosis.
|
Friedreich's Ataxia
|
|
Ipsilateral UMP signs and loss of vibration and proprioception. Contralateral loss of pain and temp below lesion.
|
Brown Sequard Syndrome
|
|
Paralysis of conjugate vertical gaze due to a lesion in the superior colliculi-
|
Parinaud Syndrome
|
|
Congenital disorder with port wine stains, ipsilateral leptomeningeal angiomas, pheochromocytomas. Can cause glaucoma, seizures, hemiparesis and mental retardation.
|
Sturge-Weber Syndrome
|
|
Hamartomas in the skin, CNS, organs; cardiac rhabdomyoma, renal angiomyolipoma, astrocytoma, mental retardation, seizures, hypopigmented spots, shagreen patch.
|
Tuberous Sclerosis - autosomal dominant
|
|
Cade au lait spots, lisch nodules (pigment in iris), optic gliomas, pheochromocytoma, Mutation in chromosome 17, autosomal dominant.
|
Neurofibromatosis Type I
|
|
Cavernous hemangiomas in skin, mucosa, organs; bilateral renal cell carcinoma, hemangioblastomas in the retina, brain stem, cerebellum, and Pheochomocytoma. AD mutation on chromosome 3.
|
Von Hippel Lindau
|
|
Vascular neoplasm of the brain with areas of necrosis and hemorrhage. Can cross the midline to the opposide hemisphere, pallisading necrosis.
|
Glioblastoma Multiforme
|
|
Most common brain tumor in adults, crosses the midline, stains for GFAP- Pleomorphic tumor cells
|
Glioblastoma Multiforme
|
|
Brain tumor that occurs in the convexities of hemispheres, has spindle cells with whorled pattern, and psammoma bodies (calcifications).
|
Meningioma
|
|
Brain cell tumor that is S-100 positive and usually found at the CP angle.
|
Schwannoma
|
|
Rare, slow growing tumor in the frontal lobes. Has chicken wire capillary pattern and round nuclei with clear cytoplasm.
|
Oligodendroglioma
|
|
Tumor in children most commonly found posterior fossa, GFAP positive, has eosinophillic corkscrew fibers, is cystic and solid. Has a good prognosis.
|
Pilocytic astrocytoma
|
|
Highly malignant cerebellar tumor in kids, has rosettes or perivascular psuedorosette. Solid small blue cells. Can compress the 4th ventricel causing hydrocephalus.
|
Medulloblastoma
|
|
Brain tumor in kids with characteristic perivascular pseudorosettes. Rod-shaped basal ciliary body found near the nucleus.
|
Ependymoma
|
|
Brain tumor in kids with famu cells and high vascularity. Most often cerebellar, associated with von hippel lundau, can produce EPO.
|
Hemangioblastoma
|
|
Benign childhood tumor with calcifications, can cause bitemporal hemianopia.
|
Craniopharyngioma- derived from rathke's pouch
|
|
Heterogeneously enhancing primary brain tumor in adults
|
GBM
|
|
Ovarian tumor with sheets of uniform cells. Secretes hCG and LDH.
|
Dysgerminoma
|
|
Ovarian tumor with large, hyperchromatic, syncytiotrophoblastic cells. Rare but malignant and can develop during pregnancy. Has increased hCG.
|
Choriocarcinoma
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Agressive ovarian cancer- yellow, friable, solid mass. Has Schiller-duval bodies that look like glomeruli. Has increased AFP.
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Yolk Sac
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Ovarian tumor, frequently bilateral, lined with fallopian tube epithelium and is benign.
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Serous cystadenoma
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Most common ovarian tumor, malignant and frequently bilateral. Has multiple cystic spaces.
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Serous cystadenocarcinoma
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This is a general ovarian cancer marker
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CA-125
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Malignant ovarian tumor, causes intraperitoneal accumulation of mucinous material from ovarian or appendiceal tumor- can be massive
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Mucinous Cystadenocarcinoma
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Ovarian tumor that secretes estrogen and can lead to precocious puberty. Has small follicles filled with eosinophilic secretions. Causes abnormal uterine bleeding.
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Granulosa cell tumor
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Triad of ovarian fibroma, ascites, and hydrothorax. Pulling sensation in the groin.
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Meig's syndrome
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Malignant, painless, testicular tumor. Most common kind, affects men 15-35. Large cells in lobules with watery cytoplasm and a fried egg appearance.
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Seminoma
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Malignant, painful, testicular tumor that is often glandular or papillary. May have increased AFP or hCG.
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Embryonal carcinoma
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Yellow, mucinous testicular tumor. Schiller Duval bodies look like glomeruli. Has increased AFP.
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Yolk Sac
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Malignant testicular tumor with increased hCG. Disordered syncytiotrophoblastic and cytotrophoblastic elements. Hematogenous mets.
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Choriocarcinoma
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Usually benign testicular tumor containing Reinke crystals, usually andrgen producing- gynecomastia in men and precocious puberty in boys. Golden brown color.
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Leydig cell.
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Most common testicular cancer in older men:
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Lymphoma
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Nephrotic syndrome with highly selective loss of albumin, lipids in tubular cells, and diffuse effacement of podocytes. Seen in young children with a URI or recent immunization.
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Minimal Change disease
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MCC of nephrotic syndrome, caused by damage of the podocytes with sclerosis and hyalinosis. IgM and C3 present but no immune complexes. Poor prognosis and high rate of recurrence in transplants.
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Focal Segmental Glomerulosclerosis
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Nephrotic syndrome with damage to the epithelial and mesangial cells by immune complex activating complement. Has a spike and dome pattern with silver stain and granular deposits of IgG and C3.
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Membranous glomerulonephritis
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Nephrotic syndrome with mixed nephritic and nephrotic features. The glomeruli are large and hypercellular. Duplication and splitting of the GBM forms tram-tracks. Slow progression with asymptomatic proteinuria and hemtaturia.
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Membranoproliferative Glomerulosclerosis
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Which four things can cause membranoproliferative glomerulonephritis?
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Autoimmune disease, infection, schistosomiasis, and malignancy,
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Nephritic syndrome developing after a skin or respiratory infection. Increased ASO and anti DNAse B. Subepithelial immune complex deposition (lumpy bumpy). Hypercellular glomeruli with IgG, IgM and C3.
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Post Streptococcal (acute proliferative)
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Nephritic syndrome with hypercellular glomeruli with granular deposits of IgG, IgM and C3. Kidneys are enlarged and swollen with multiple surface punctuate hemorrhages.
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Post-streptococcal
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Nephritic syndrome caused by ruptures in the GBM with infiltration of leukocytes, fibrinogen and parietal epithelial cells. Has three types:
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Rapidly Progressive (cresentic)
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This type of rapidly progressive glomerulosclerosis has antibodies to GBM, with smooth, linear staining of IgG and C3.
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Type I RPGS
-if it has lung involvement, its Goodpastures |
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This type of rapidly progressive GS has immune complex deposition and granular staining of IgG and C3
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Type II
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This type of rapidly progressive GS is ANCA positive and may be caused by vasculitis like Wegeners and Churg Strauss
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Type III
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Characterized by nephritis, hearing loss and ocular abnormalities. Is an X-linked recessive defect in type IV collagen. Has irregular thickening and thinning of the GBM with splitting.
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Alport Syndrome
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MCC of nephritic syndrome worldwide. Causes painless, recurrent hematuria in kids, 1-2 days post infection of mucosal tissue. Is associated with HSP, celiac sprue, and dermatitis herpetiformis
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IgA nephritis
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