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594 Cards in this Set

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Nephritic syndrome following upper respiratory syndrome
IgA Nephropathy
Most common cause of nephrotic syndrome in children?
Minimal change disease
Oliguria, azotemia, elevated BUN and Cr, RBC casts, HTN, hematuria, often post URI.
nephritic syndrome
Nephritic syndrome with RBC casts, edema and HTN
Glomerulonephritis
Muddy brown casts and renal failure
Acute Tubular necrosis
papillary necrosis, polyurea with sterile pyuria, patient taking NSAID
analgesic nephropathy. Also can be caused by hemophilia, DM, cirrhosis or CHF.
cystic liver on u/s, patient is on dialysis, palpable kidneys.
polycystic kidney disease
infant with hypocalcemic seizures, congenital heart disease, anomalies of great vessels, MR, esophagela atresia, low set ears
DiGeorge's Disease. Due to defect in pharyngeal pouches.
X linked disease presents after 6 months of age with incapsulated invections ie H flu and S. pneumoniae, low Ig levels and few B cells on smear.
Bruton's Agammaglobulinemia. Similar presentation to CVID but CVID not sex linked, presents in teenage years and normal B cell number.
Predisposing factors of Acute/Subacute Bacterial Endocarditis?
-MVP
-Deg Vasc disease
-IV Drug Use
-Prosthetic Valves
-Congenital abnormalities
How long does etoh withdrawal take?
presents 12-24 hours after last dirnk with DTs 2-4 days out. Autonomic instability, tachycardia, fever, sweating, tremor and hyper reflexia.
What is a Charcot's Joint?
Neurogenic arthropathy ... joint destruction due to loss of pain, temp and proprioception. Due to diabetes, spinal cord injiury, peripheral nerve disease or tabes dorsalis.
Strokes
1. happening during exercise with focal neuro signs, HTN
2. previous TIA, hyperlipidemia, DM
3. severe headache
1. hemorrhagic
2. ischemic
3. SAH
Acid fast filamentous branching rod causing pulmonary or cranial cavitary lesions.
Norcardia. Not TB. TB is a GNR acid fast bacilli no branching.
Treatment of hypercalcemic crisis?
IV lasix and fluids.
NTD are seen with what drug?
Valproic acid predisposes to neural tube defects and cardiac anomalies, midface hypoplacia and cleft lip.
Cough with hemoptysis and infiltrates + proteinuria and ARF and dysmorphic RBCs. What test do you do to confirm?
Goodpastures. Do renal biopsy showing IgG on Glom BM
Prophylaxis for pertussis?
erythromycin for 2 weeks for everyone! Even if immunized. 75% of people get symptoms.
Mid diastolic rumbling murmur loudest at the apex of the heart
Mitral Stenosis most commonly from rheumatic heart disease.
Direct vs Indirect Coombs Test
Direct- for hemolytic anemia, put washed RBCs in coombs reagent, if they agglutinate there was bound Ig = +
Indirect- Looking for free Ig against RBC ie Rh status in pregnancy.
How do you test for paroxysmal nocturnal hemoglobinuria?
Sugar water test
5 types of lactate dehydrogenase?
1 heart and RBC (hemolytic anemia)
2. reticuloendothelial
3 lungs
4 placenta,kidneys, pancreas.
5 liver and muscle
Most common presentation of heterozygous sickle cell trait?
painless hematuria
HbS usually 40%
Treatment of fibromyalgia
TCA at night low dose amytriptyline.
Treatment of cat bite? Concerning organism and possible complication?
Bacillary angiomatosis ... skin lesion with growth of blood vessels due to Bartonella a gram negative rod from cat bites that needs treatment with erythromycin.
major side effect of olanzapine (atypical antipsychotic)
weight gain... diabetes
major side effect of clozapine (atypical antipsychotic)
agranulocytosis.
Headache following OM ... next step in management.
Concerning for intercranial abscess get head CT for ring enhancing lesions.
palsy following a seizure... treatment?
Todd's palsy will resolve no tx
+ Romberg's sign indicates what?
peripheral nerve damage causing sensory ataxia. Can also indicate cerebellar disorder will falls toward the affected side.
You note hypersegmented neutrophils and a megaloblastic anemia. How do you differentiate between folate vs coalbamin B12 deficency?
Coalbamin is needed to conver methylmalonyl co A to succinal Co A so if B12 is low there will be increased methylmalonic acid levels as well as elevated homocysteine levels (B12 and folate are both needed for conversion of homocysteine to methionine)
Treatment of stable angina?
1 BB
2 CCB
What disease process causes paratracheal adenopathy and noncaseating pulmonary granulomas as well as anterior uveitis, polyarteritis and erythema nodosum (vasculitis)? What is tx?
Sarcoid.
Treatment is with glucocorticoids.
Pulmonary lesions in person traveling to Ohio/Missippi River Valley to go Spelunking?
Histoplasmosis. Treatment wiht Itraconazole.
Infliximab
TNF alpha blocker, treats IBS, Ankylosing spondylitis and RA
You note an elevated alk phos, bone pain and mosaic pattern of lamellar bone in an elderly gentleman. What are you concerned about?
Pagets disease of bone. Increased bone turnover due to osteoclast hyperactivity.
Interpret high vs low alk phos values.
High alk phos- either liver injury ie stones or bone ie Paget's
Low alk phos- incidicates CML or paroxysmal nocturnal hemoglobinurea
Brick red maculopapular rash, moving from face down, conjunctivits, fever, coryza. What is it and what vit do you give?
Measles. Give Vit A.
LAD especially posterior cervical and posterior occipital, low fever, red maculopapular rash starting on face moving down.
Rubella. More L's = lower fever more lymphadenopathy.
Strawberry tongue and red red eyes in a child.
Kawasaki's Disease medium vessel vasculitis.
Loss of pain and temperature in cape like distribution. Seen in many pt after spinal cord injury ie MVA with wiplash.
Syringomyelia due to cust of CSF fluid.
What tract?
vibration and position
pain and temp
motor
vibraiton and position = dorsal column
pain and temperature = spinothalamic
muscle/motor strength = lateral corticospinal tract, decending
Loss of pain/temp contralaterally below lesion, loss of motor, proprioception and vibration ipsilaterally.
Brown Sequard hemisection of cord.
paraplegia, incontinence, saddle anesthesia
cauda equina syndrome
2 Drugs of choice treating HTN in pregnancy.
What if pre eclampsia?
Treat BP with hydralazine (direct vasodilator) and labetalol. Avoid diuretics.
If pre eclampic also use M but this is to decrease risk of future seizures not to treat BP, important distinction.!
Treatment of uncomplicated UTI in nonpregnant patient?
Bactrim
Goal tidal volume for ventilator?
6 ml/kg
crecendo decrescendo systolic ejection murmur at 2nd intercostal space on the right radiating to the carotids.
Aortic stenosis- also radiates to the carotids, weak S2, often LVH and S4 and displaced PMI due to LVH.
wavy lines acorss the vision with loss of central vision.
wet macular degeneration due to new blood vessels
patient experiences tunnel vision. fundoscopic exam shows cupping of the optic disc
open angle glaucoma... high IOP with tunnel vision and cupping of optic disc.
Sudden loss of vision "shade like" darkness
emergency! retinal detachment, usually with myopic patients and after trauma.
Location of lesion for patient presenting with expressive aphasia ie Brocas
left frontal lobe consider left MCA infarct
pathophysiology of Zenker's diverticulum?
esophageal herniation due to dysmotility and incoordination between esophagus and pharynx. older individual presenting with neck mass when dirinking fluids.
definition of fetal deceleration
decrease in fetal HR of at least 15 beats for 15 seconds
infant with colickly abdominal pain, vomiting, red jelly stools, feel saussage shaped mass in abdomen. Treatment?
Give air contrast enema for intrasusseption.
Organism most likley causal for osteomyelitis? What if sickle cell?
1. S. aureus (less likely GBS, E coli , S pyogenes)
2. Salmonella in sicle cell
Drug cause of priapism?
prazosin causes priapism.
(alpha blocker)
Second most likely cause is Trazadone then trauma, neurogenic, sickle cell or leukemia.
Soft S1 3 days after MI, murmur loudest at apex with radiation to axilla, pansystolic.
Suspect mitral regurgitation to to papillary muscle rupture. Biggest risk 3-7 days after MI for free wall rupture and papillary rupture.
This acid fast filamentous branching rod causes pulmonary cavitary lesions and infections in the immunocompromised. Treatment is with Bactrim. Not TB!
Norcardia =acid fast branching rod
TB = acid fast bacilli
Baby is born with neural tube defects, cardiac anomalies, dysmorphic facies, cleft lip and midface hypoplasia. What drug was he exposed to inutero?
Valproid acid exposure leads to NTD.
Side effect of clozapine?
agranulocytosis
Main side effect of olanzapine?
seight gain.
How does CML present?
CML presents with leukocytosis, anemia, increased neutrophils and bands on peripheral smear. Usually older individual with night sweats, malaise, feer, weight loss, anorexia and bone pain. Often low alk phos.
This disease is due to oxidative damage to th elens with aging resulting in thickening and clouding of the lens.
cataracts.
What is Boorhave syndrome?
spontaneous rupture of esophagus usually seen in slcoholics after severe vomiting with patient having severe retro sternal pain.
Name 3 tests that look at liver function
liver function, PT, bilirubin, albumen, cholesterol synthesis.
Name tests that look at structural integrity of the liver.
GGT, LFTs and alk phos. Marked increase indicates ongoing tissue destruction. Progressive decrease indicates few functional hepatocytes. Look for 2:1 ratio of AST to ALT in ETOH.
variable deceleraitons are due to what?
fetal cord compression = variable decels
early deceleraitons (same time as the uterine contraction, uniform in shape) indicate what?
fetal head compression during the ocntraction = early decel
What does early fixed splitting of the heart sounds indicate?
ASD- blood is flowing from the LA to the RA so the pulmonic valve takes longer to close due to the increased pressure gradient.
Pulses parvus et tardus (slow late carotid pulse) indicates what?
aortic stenosis
What is Kussmal's sign
increase in JVP with inhalation indicating pericarditis or right ventricle infarction, backing up of blood into venous system.
Why are SGA infants at higher risk for polycythemia?
increased hypoxemia results in more erythopoietin and more RBCs.
Reglan (metocloperamide), typical antipsychotics, prochlorperazine can all cause what side effect?
Torticollis.
Your patient is in shock but has an elevated PCWP > 10 with hypotension. What do you give?
The patient is in cardiogenic shock. Give lV fuids and then ionotropes to increase CO. Elevated LA pressure is due to backup pressure from heart failure.
Causes for elevated PCWP? Normal PCWP 8-10.
cardiogenic shock or obstrution. Anything preventing the forward flow of blood.
What does a low mixed venous oxygen concentration mean (MVo2)?
increased oxygen extraction by hypoperfused tissues as in neurogenic or hypovolemic shock. In septic shock MVo2 can be normal as their is a distribution inequality along the tissues.
Most comon cancer from aspestos exposure? (pulmonary fiborsis, weight loss, wheezing, dypsnea, pleural plaques).
Bronchogenic carcinoma. Arsenic exposure occurs with mining, ship building, insulation, pipe work.
Sturge Weber Syndrome?
Port wine stain along trigeminal nerve, seizures and retardation. Often intercranial calcificaitons resembling a tramline . Defect is proliferation of arteries in teh brain resulting in ulilateal hemaniopsia and hemiparesis.
Cut off for neutropenia?
ANC < 1500. If below 1500 always give abx even with simple fever and no s/s of infection.
pale velvity pink or white patches, scale when you scrape them and don't tan.
Tinea versicolor. Treat with ketoconazole or selenium sulfide.
what aretery is teh first division of the internal carotid?
opthmologic artery. If retinal artery occlusion at terminal branch amarosis fugax can occur. Treat with 100% O2 and massage.
Diastolic decrescendo murmur along the LL sternal border.
aortic regurgitation.
How does the respiratory quotient depend on the fuel being consumed for energy?
RQ = CO2/O2 use.
If RQ is close to 1 = carbs
Proteins = 0.8
Lipids 0.7
If excessive feeding of venitilated patients with carbs they are more difficult to wean due to additional CO2 production.
Fever, cough, coryza, conjunctivitis and Koplik (blue /white spots on red background) spots = ?
Measles = koplik blue spots
Slapped cheeks rash?
5th's disease due to parvovirus B 19. Sicle cell crisis can be caused.
This X linked disorder (seen in males) is characterized by eczema, thrombocytopenia and hypogammaglobulinemia.
Wiskott Aldrich Syndrome
treatment of Tourette's?
typical antipsychotics such as haloperdol and pimozide treat Tourette's.
Triad of congenital toxoplasmosis ?
chorioretinitis, hydrocephalitis, intercranial calcificaitons (contrast with Rubella which has cardiac defects and deafness)
Triad of congenital Rubella?
deafness, cardiac defects, cataracts. (contrast with toxo which has intercranial calcifications)
If you push on a child's medial canthus and expell pus what is the infection?
Dacryocystitis- infection of the lacramal sac
Absess on the upper eyelid by s. aureus?
Hordeolum.
Chronic granulomatous infection of the meibomian gland- hard painless uppe reyelid nodule?
Chalazion.
Older woman with dysuria, painful sexual interourse and deficaiton, white polygonal macules and patches. Vulva is thin, whte and dry. What do you suspect and why must you get a biopsy?
Concern is for SCC of teh vulva. Most likely Lichen sclerosis but still need to biopsy. Then streat with steorids.
What does it mean if the relative risk crosses 1?
No association between the risk factor and the disesae.
What does it mean if the conficence interval contains the value 1.0?
The value 1.0 is null such that there is no significance if CI contains 1.0
When do you give Tetanus toxoid vs. Ig
Ha s the patient had 3 or more vaccinations withing the last 10 years. If yes then you only need to give TT if the wound is dirty. If last vaccination >5 years ago then give TT even if wound clean. If the wound is dirty and the patient has had < 3 vaccinations give TT and tetanus Ig.
What causes paresthesias after a patient gets multiple RBC transfusions?
Citrate chelates the calciumin teh blood causing transietn hypocalcemia after transfuions.
An infant has conjunctivitis. Based on time of presentation how do you determine what it is (gonococcal, allergic or chlamydial)
allergic - first 24 hours
Gonococcal 2-5th day (ceftriaxone)
Chlamydial- day 5-14, purluent discharge and RN (oral erythromycin due to risk of PNA)
Treatment of resting tremor, bradykineska and rigidity of parkinson's disease
Anticholinergics such ans benzotropie increase ACh which helps improve PD tremor.
How Teat for autoimmune hemolytic anemia?
Coombs test. Anemia is uaully preceeded by URI in children 2-12 yo.
Your patient has dilated pupils, ileus, seizures and long QRS. What do you give them and what did htey OD on?
PD on TCA ie amytriptalyine.
Give bicarbonate to improve BP and to narrow th QRS to reduce risk of arrhythmia.
Treatment for patients with Torsades due to a long QR interval?
Mg Sulvate treats long QT interva..
How do you treat the SLUDGE of organophosphate poisioning?
Atropine and pralidoxine.
Pralidoxine binds to Acetylcholinesterase so that available ACh is not degraded.
Atropine increases BP and HR.
Also Benzos to reduce risk of seizure.
Common findings in anorexic patients
Anorexia associated illness
osteoporosis
elevated cholesterol and carotene
long QT
euthyroid sick syndrome
anovulation and amenorrhea
hyponatremia- due to increased H20 intake.
What causes stress fractures?
repeated exhertion ie on heel from running
Age >40, triad of systemic vaculitis, upper and lower airway granulomas and GN.
(epitaxis, nonhealing granulomatous lesions, pyoderma, RBC casts proteinuria, ANCA positive)
Wegner's granulomatosis
treat with cyclophosphamide
puncture wound through rubber shoe = infection with?
Tx?
pseudomonas. Treatment with FR such as levofloxacin.
What is a counterindication to giving a SERM such as Raloxifene?
Prior DVTs are counterindicated with raloxifene. Serms are a mixed agonist in the bone and an estorgen antagonist in the breast and vaginal tissue.
Do SERMS increase the risk for breast or endometrial cancer?
Tamoxifen increases the risk of endometrial cancer. Raloxifene and Tamoxifen reduce the risk of breast cancer and improve bone density.
Differential for T wave inversion:
MI, myocarditis, old pericarditis, myocardial contusion, digoxin toxicity
10 yo boy comes in with multiple skin infections from s. aureus in his history. What immune defect do you suspect?
Suspect defect of phagocytic cell to make oxidative burst with NADPH- test with nitro blue tetrazolium.
Young boy with eczema, thrombocytopenia and bacterial infection with H. flu or other encapsulated organism. He bruises easily and antibody levels are variably decreased.
Wiscott Aldrich syndrome
x linked immunodeficency
eczema, thrombocytopenia and recurrent encapsulated bacterial infections.
Girl with absent thymic shadow, lymphopenia, recurrent fungal and bacterial infections in first year of life.
SCID- severe combined immune deficency
patient has multiple pulmonary infections and diarrheas as well as a recent reaction to blood products.
IgA deficiency. Deficient mucosal border protection as well as anaphylaxis to blood products.
Kartanger's syndrome
ciliary dysfunction resulting in recurrent otitis, sinusitis, URIs and infertility
Addison's disease
hyponatremia, hyperkalemia, anemia, esoinophilia, weakness, increased pigmentation, anorexia. Test with cosyntropin test (ACTH analogue) see if there is primary or secondary adrenal insufficency.
tall stature, crowded teeth, long limbs, arachnodactly, mutation of fibrillin...
Marfan's (AD with variable penetrance)
Ehler's danlos is a mutation in what?
Mutation in collagen resulting in poor healing, hyperflexible joints, easybruising and hyper elastic skin.
Baby with rocker bottom feet, small head and low ears.
Edwards trisomy 18
first line treatment of generalized anxiety?
Buspirone (Buspar) partial serotonin agonist. then consider venlafaxine (serotonin andNE reuptake inhibitor) or Lexapro (SSRI)
What kind of bias is caused by losing patients to follow up?
Selection bias- possibility those individual lost to follow up differin their development of the outcome measure - perhaps more compliant patients to treatment are less likely lost to follow up.
Why do patients with renal failure have platelet dysfunciton?
How do you treat it?
uremic toxins cause platelet dysfunciton prolonging bleeding time (Pt,PTT, INR are normal). Treat with desmopressin which releases BIII and Von Willebrand factor from storage.
Name 4 causes of a macropapular rash.
Macropapular rash seen in scarlet fever, measles, parvovirus andheat rash.
vibration and proprioception?
motor ?
pain and temp?
vibration and proprioception are posterior dorsal columns cross in medulla
Lateral corticospinal tract is muscle strength which crosses in medulla and is descending.
Spinothalamic tract is pain and temperature and crosses within two spinal segments.
Definition of pre eclampsia
HTN >160/110, proteinuria <5g/24 hrs, pulmonary edema, thrombocytopenia and elevated liver enzymes
Describe assist control ventilator setting.
In AC a tidal volumeis delivered to the patient whenever the patient initiates a breath or at a baseline rate if the patient fails to trigger the vent.
Murmur? Crescendo decrescendo systoli cejection murmur at the 2nd intercostal space on the right, radiating to teh carotids. dyspnea, syncope, angina on exhertion.
Aortic Stenosis.
How does retinal detachment present
like a shade falling in front of the eye, sudden loss of vision.
Disorder of cilia, results in otitis, sinusitis and repeated URIs
Kartagener's syndrome- dysfunctional cilia.
Patient has hyponatremia, hyperkalemia, weakness, pigmentatino, anorexia. ??
Addison's. Diagnose by cosyntropin test. If cortisol rises you can rule out primary adrenocortical insufficency.
In addition to aspirin what drug decreases mortality after an episode of unstable angina or NSTEMI?
Patient should be on both clopidogrel and aspirin for 12 months.
What is anoscopy?
Visualizes teh rectum to look fo hemorrhoids.
Symptoms of a pinealoma?
The pineal gland makes melatonin so tumor can cause insomnia, also precocious puberty and paralysis of CN III.
Patient presents with diarrhea, leg cramps 2/2 hypokalemia and low stomach acid. Termed teh pancreatic cholera.
VIP oma causes diarreha and hypokalemia.
liver cysts + blood diarrhea + foreign travel.
Amebiasis Histoliticus-. Due to trophozoites. Test stool. Treat with metronidazole.
Treatment of chlamydia
single dose azithromycin or 14 days of doxycycline
Treatment of Gonorrhea
ceftriaxone .
Endocrine disorder (immunologic, testicular atrophy, baldness, hypothyroidism) and proximal and distal muscle weakness (thin face, temporal wasting)
Myotonic muscular dystrophy (is autosomal dominant)
What typical antipsychotic can cause hypothermia by inhibiting the shivering mechanism?
Fluphenazine.
Most common cause of communicating hydrocephalus in premature infants?
Sub arachnoid hemorrhage.
Treatment of cryptoccal meningitis.
IV amphoteracin and flucytosine.
Treatment of cat bites with concern for Pasturella moltocida?
amoxicillin and clavulanate for 5 days.
Why are Floroquinolones not used in children?
risk of tendon reupture.
In a low pH environment is free calcium high or low?
Calcium is released from albumen in low pH environmentt so unbound Ca would be higher.
In a alkaline environment ie altitude claicum is bound to albumen resulting in transient paresthsias
MEN II a syndrome
Due to Ret oncogene.
medullary thyroid cancer, pheochromocytoma, parathyroid hyperplasia.
Men IIB
medullary thyroid cancer, pheo, mucosal neuromas.
Virchack's node, elevated bilirubin, increased alk phos, weight loss, epigastric pain, jaundice.
pancreatic cancer. Get abdominal CT to evaluate.
Signs of Niacin B3 deficency
pellagra- dermatitis, dementia and diarrhea
Glasgow Coma Scale
Eye opening 1(none to spontaneous 4
Verbal none 1 to oriented 5
Motor none to obeying command 6
Treatment of dystonia from haloparadol?
antihistamines or anticholinergics ie diphenhydramine or benzotropine.
Patient with nasal polyps, chronic sinusitis, anosmia, nasal obstruction and shortness of breath.
Suspect NSAID induced bronchospasm ie from Aspirin.
Triad of parkinson's disease
bradykinesia, resting tremor, rigidity
Eczema, thrombocytopenia (bleeding and bruising) and recurrent respiratory infections ... male child.
Wiskott Aldrich Syndrome
Boy with recurrent infections with staph aureus and pseudomonas and other catalase positive organisms. What test do you want.
Nitroblue tetrazolium dye tesst for chronic granulomatous disease. X linked due to NADPH oxidase inactivity.
Most common infection with complement deficencies?
Neisseria.
Recurrent staph infections of the skin, fair hair, eczema, high IgA levels.
Job hyper IgE syndrome
albinism and dysfunctional neutrophils with giant granules?
Chediak Higashi Syndrome due to a defect in microtubule polymerization.
Patient has rigidity, mutism, obtundaiton, agitation, high fever, high creatine phosphokinase, sweating , myoglobinuria and is on an antipsychotic. Waht do you do?
Give dantrolene just like in malignant hyperthermia.
side effect of antipsychotic Thioridazine?
retinal pigment dposits
side effect of antipsychotic clozapine
agranulocytosis
side effect of antipsychotic chlorpromazine
causes jaundice and photosensitivity
personality disoder of bizarre beliefs, likes witchcraft, superstitious.
Schizotypal personality disorder
The classic loner, no friends and no interest in having them
Schizoid personality disorder
No friends but wants to have them, afraid of criticism or rejection, inferiority complex.
Avoidant perosnality disorders.
Tratment for narcolepsy?
Modafinil or amphetamines.
First line tratment for gerneralized anxiety disorder?
Buspirone then SSRI then Benzos.
Treatment for ADHD
stimulants such as modafinil, methylphenidate (ritalin) or dextroamphetamine.Use drug holidays when possible to decrease side effect.
What is the best test for comparing two means?
What about two percentages?
t test compares means
Chi square test compares 2 percentages.
Treatment of chlamydia in pregnant woman?
In non pregnant women?
erythromycin or amoxicillin if pregnant.
Doxycycline if not pregnant.
Single dose treatment for chlamydia?
1 g oral dose of azithromycin.
Malodorous vaginal discharge with fishy smell on KOH, clue cells. Treatment
Treat with metronidazole for Gardnerella vaginialis.
Treatment of Neisseria gonorrhoeae for mucopuruent cervicitis with gram neg diplococci on smear.
Ceftraixone or ciprofloxacin. Always treat for assumed Chlamydial infection with doxycycline as well. If patient has Chlamydia then you don't need to assume gonorrhea!
Painless chancre, spirochete on dark field microscopy, treatment?
Treatment ofr primary syphilis is penicillin.
Condyloma lata, maculopapular rash on palms, treatment?
Treat secondary syphilis with penicillin.
Pale frothy watery discharge with strawberry cervix. Bugs can be seen swiming under microscope. Treatment?
Metronidazole for Trichomonas vaginalis.
What is the most common defect in CAH?
-salt wasting (low Na)
-hyperkalemia
-hypotension
-elevated 17 hydroxyprogesterone
21 Hydroxylase deficency.
PAtient with "bunch of grapes" protrusion from vagina?
sarcoma botryoides a rhabdomyosarcoma malignant tumor
Most common cause of secondary amenorrhea?
prengnacy.
What is Chadwick's sign?
Blue dark discoloraiton of the vulva and vaginal walls inpregnancy.
Congenital Rubella syndrome?
deafness, cataracts, cardiac abnormalitis.
Positive tripple screen in pregnancy with low AFP, low estriol, high hCG means?
Downs syndrome.
What is the fourth value in a quad screen of pregnancy and what value (high/low) indicates Downs?
High inhibin A indicates Down's.
What does a low AFP mean?
High AFP?
NTD is high AFP while Down's is Low AFP
What do you do if a tripple screen is positive at 16-20 weeks?
Do an amniocentesis.
Earliest screen at 9-12 weeks?
chorionic villus sampling, reserved for women with previously affected offspring or known genetic disease.
Most common TORCH infection: small eyes, cerebral calificaitons, deafness
CMV infection.
What is potter's disease?
Fetal bilateral renal ageneiss. cause of oligohydramnios. Often presentatino is with hypoplastic lungs and acute respiratory distress first.
Early sign of Mg toxicity?
hyporeflexia followeed by respiratory depression, coma and death.
What test determines fetal vs maternal blood incases of painless vaginal bleeding during pregnancy?
The apt test. Concern for vasa previa or velamentous insertion of the cord.
Amniotic Fluid Indes < 5 is vs > 25
polyhydramnios vs oligohydramnios. Measures the four biggest vertical pockets of fluid in each quadrent.
Treatment of chorioamnionitis?
Ampicillin.
Treatment of mastitis... most common organism is staph aureus.
cephalexin or dicloxacillin
What is a real number?
A real number is the set of numbers that includes all members of the set of rational numbers and all members of the set of irrational numbers.
Real Numbers = Rational Numbers + Irrational Numbers
vertigo+ tinnitus + hearing loss =
Meniere's disease. Treat with anticholinergics and antihistamines.
How many Hep B vaccinations and Hib before 1.5 years
3 doses by 1.5 yrs for Hep B and 4 doses HiB
DTP how many doses by 6 years?
5 doses by 6 tears
Polio how many doses by 6 years?
4 doses
HWhen do you give Varicella vaccinatoin and when do you avoid it?
Avoid if immunosupressed due ot live vaccine oterhwise give at 1-2 years
What vaccines have eggs ?
Influenza, MMR all have eggs.
+ Babinskis
upward fanning of the toes, indicates UMN disesae
Beck's triad
JVD, mufflec heart sounds, hypotension. Indicates pericarditis
Cushing's reflex
HTN, bradycardia and irregular respirations make you think of hemorrhage or increased ICP
Homan's sign.
calf pain with forced dorsiflexion of foot with DVT
Kehr's signq
left shoulder pain with ruptured spleen (any irritation of the diaphram)
Murphys sign
arrest of inspiration when palpating the RUQ in cholecystitis.
Verner Morrison syndrome
watery diarrhea, achlorydia and hypokalcemia due to pancreatitic tumor secreating VIP (VIPoma)
Bitot's spots
Vit A deficency
Bronze diabetes
hemochromatosis look for cardiac and liver dysfunction
cherry red maculaa
tay sach's or niemann pick (self injury and HSM)
friction rub ?
pericarditis
heliotrope rash
dermatomyositis
increased hemoglobin A2 + anemia (basophilic stipling and target cells
thalassemia
meconium illeus , salty baby, rectal prolapse
CF
freckling around lips and increased risk for colon cancer
peutz jeghers disease.
Does the pneumococcal vaccine require T, B or both cell response?
pneumococcal induces a T cell independent response due to itspolysaccharide capsule whcih independently activates B cels.
What do you need to remove a foreign body from the lung?
A RIGID bronchoscope.
Tick bite + wrists and ankles rash, fever, malaise, HA, leukopenia and thrombocytopenia
Erlichosis aka RM spotted fever
Northeaster US, jaundice, hemmoglobinurea, renal failure and death possible. Worse if older and asplenic. Look for atypical lymphocytes, anemia and abnormal LFTs
Babesiosis due to tick. causes direct RBC hemolysis due to the parasite.
Treatment of UTI in pregnancy?
amoxicillin, nitrofurantoin or cephalosporin.
Treatment of pylonephritis
?
ciprofloxacin.
+ Tzanck smear?
Herpes virus
If your HIV patient with pneumonia is allergic to sulfa what do you give?
Can't give bactrim so give pentamiddine for PCP.
Flu like syndrome with hepatitis and pneumoniae in an animal exposed person ie vet or goat herder, what is it?
Q fever from Coxiella.
You have a young patient suddenly present with CHF. What do you suspect?
Myocarditis usually with Coxsackie B virus.
Desert rheumatism of SW US aka Valley fever seen in Arizona, Texas is due to what?
Coccidiomycosis00 fungal infection causes flue like symptoms, pneumonia and rashes.
Person indifferent to friendships, magical thinking, aloof.
schizoid personality disorder.
Nasty enlarged tender inguinal lymph nodes ?
Lymphogranuloma venereum, aspirate the node, treat with doxycycline, watch for drainage tracts.
Yellow purluent urethritis, what is it and tx?
Gonorrhea. Give single dose azithromycin or ceftriaxone.
What is tenosynovitis and give example.
Tenosynovitis ins inflamamtion of fluid filled sheath of the synovium around the tendon (tendon tethers muscle to bone) example is De Quervain tenosynovitis of thumb or trigger finer.
Most common cause and location of endocarditis in IVDU
tricuspid valve R heart with S. aureus. Normally think mitral valve with S. viridans.
Liver enzymes in ETOH hepatitis
AST/ALT > 2/1
psammoma bodies, ground glass cytoplasm, good prognosis as far as thyrroid cancer is concerned.
Papillary thyroid cancer = psammoma bodies
this thyroid cancer has early hematogenous spread and invades blood vessels.
follicular thyroid cancer. BAD news.
Most common cause of hypothyroidism in US ?
hypoplasia or dysgenesis.
Young fat female on Isotretinoin with headaches.
Think pseudotumor cerebri, VitA predisposes.
Midsystolic click=
mitral valve prolapse
diffuse ST elevation, PR segment elevation in aVR, pericardial friction rub
pericarditis. Pericarditis 2/2 renal failure get dialysis.
Microcytic anemia MCV < 80 with basophilic stipling
Lead posioning
Anemia with elevated MCV and hypersegmented neutrophils, basophilic stippling, poikocytes, low reticulocyte count
B12 deficency or folic acid eficency.
Bullous pemphgoid
tense blisters at flextural areas, elderly patient with uticaria. UV radiation, abx or NSAID use. Pattern of C3 and IgG linear deposits at dermal epidermal junction.
IgG deposits intracellularly causing blistering with flaccid bullae including in the oral mucosa
pemphigus vulgaris.
pituitary dysgenesis with anosmia?
Kallman's syndrome = hypogonadotropic hypogonadism
cafe au lait spots + polyostotic fiberous dysplasia and precocious puberty (possibly other endocrine disorders) often MR
McCune Albright.
afraid but wants friendships, feels inferior, sensitive to criticism
Avoidant personality disorder.Avoids failures.
High levels of androgens and estrogens predisposes women with PCOS to what type of cancer?
Endometrial cncer - think unopposed estrogen. These women have very low progesterone.
Normal <18 PCWP, respiratory difficulty, PaO2/FiO2 <200. bilateral fluffy infiltrates.
ARDS due to inflammatory mediators incresing alveolar permeability.
Hemolysis after primaquine or sulfa drugs in person from Mediterranean origin?
Glucose 6 phosphate dehydrogenase deficency.
Risks of drug treatments for Graves PTU vs Methimazole
PTU can cause dose independent hepatitis and vasculitis whiel Methimazole causes dose dependent cholestatic jaundice.
apraxia vs agnosia
difficulty carying out activities is apraxia while agnosia is difficulty recognizing objects.
weird, wet and wobbly.
normal pressure hydrocephalus.
Neer's sign = impingment sign = pain when raising arm after pretending to pour out beer means?
Subacromial bursitis. Seen in repetative overhead movements ie tennis.
Most common cause of SAH in children?
AVM with rupture.
acid base derangements in seizures?
1. post ictal hypovenitlation causes respiratory acidosis.
2. lactic/metabolic acidosis from prolonged muscle contractions.
Normal AFP, young woman with OCP use and single liver mass.
Hepatic adenomas.
Treatment of SIADH 1 and 2
1. fluid restriction
2. Demeclocycline by causing DI
chelitis (chapped lips), stomatitis( inflammed mouth) glossitis (swollen tongue) + anemia. What vitamin is lacking?
Riboflavin B2 deficency. Rare unless celiac or anorexic.
Night blindness, dry corneas, dry scaly skin, bitot silver spos on conjucntiva = what vit deficency
Vit A
fruity breath is ?
either keytones ie DKA or ammonia and liver failure
Risk of inheriting bipolar disorder
-5-10% if first degree relative
up to 60% if both parents have bipolar
only 1% in general population.
triad of ataxia, skeletal deformities and cardiac deformities.
Friederich ataxia, note scoliosis, hammertoe, HOCM, dysarthria, gait ataxia.
2 causes of non anion gap metabolic acidosis
Diarrhea and renal tubular acidosis
Causes of metabolic acisosis with anion gap?
MUDPILES- methanol, uremia, DKA, paraldehyde, INH, lactic acidosis, salicylates.
Causes of metabolic alkalosis
vomiting and hyperaldosteronism
Diarrhea, most common cause in
1. young child <2 yo
2. adults
3. bloody diarrhea
4. travelers
1. rotavirus
2. campylobacter
3. Shigella
4. E coli
What is coronary steal?
CCB can't dilate diseased sclerotic blood vessels so other regions are better perfused.
First step in primary amenorrhea workup?
Get FSH. If FSH is high get Karyotype since pituitary axis is working... concern for male gonadal agenesis or Turner's.
Splenomegaly, thrombocytopenia, anemia, older patient with lymphadenopathy. SMUDGE CELLS.
CLL = Smudge cells
Marfans + mental retardation + thromboembolic events = ?
homocysteinuria. Treat with high dose vitamin B6. Autosomal recessive disease
phenylalanine hydroxylase deficency, buildup of phenylalanine, mental retardation, fair complexion, ecxama, musty body odor
PKU
cherry red macula, weakness, seizures, mental retardation. Due to hexosaminidase A deficency.
Tay Sach's (sphingolipidosis)
mental retardation, blindenss, deafness, paralysisi, neuropathy, eizures. Absence of myelin sheath due to galactosidase deficency.
Krabbe's Disease
PAtient has acne,erythrocytosis, gynecomastia, azospermia, decreased testicular size, cholestasis, hepatic failure and dyslipidemia. What do you expect levels of FSH, LH and GnRH to be?
Expect low FSH, LH, GNRH and testosterone levels. Endogenous testerone does not show up.
This chromosomal disorder causes decreased axial skeletal growth, gynecomastia, azospermia and primary hypogonadism. Expect high FSH and LH but low testosterone due to testicular fiborsis and seminiferous tubule dysgenesis.
Kleinfelter syndrome XXY
What is the abnormality with Factor V Leiden?
Point mutation in Factor V causing resistance to inactivation by protein C. Most common hypercoagulable disorder often DVT risk is the herald or multiple miscarriages.
If you are concerned about alcoholic verices what medication do you give?
BB
Most common form of CAH?
21 hydroxylase deficency has excess of 17 alha dydroxyprogesterone which regults in virilizism and hyponatremal and hyperkalemia (salt wasting)
Most common cause of nephritic syndrome in children?
minimal change disease is the most common cause of nephritic syndrome in children. Respond dramatically to steorids.
Most common cause of nephritic syndrome in adults, note thickening of basement membrane and subepithelial spikes on EM.
Membranous glomerular nephritis.
3 diseases where you see noncaseating granulomas.
1. Chrons
2. TB
3 Sarcoid
4. Yersinia
IBD with skip leisons, colon involvement, cobblestoneing, creeping fat, fistuals , perianal disease, rectal sparing, noncaseating granulomas.
Chron's Disease
Cause of polyurea... associated hyponatremia, low serum osmolarity and high urine osmolarity.
SIADH
Elevated serum osmolarity, dilure urine with low osmolarity <3000, polyurea cause?
DI - resistance to ADH nephrogenic or no ADH production (central)
Preterm infants with respiratory distress who present with increased gastric residues.
Necrotizing enterocolitis. Present wiht bloody stools.
PFTs, obstructive vs restrictive disease?
obstructive ie asthma or emphysema has a low FEV1/FVC <0.80, while restrictive disease ie fibrosis has ratio >0.8.
In both cases FEV1may be decreased but in obstructie disease it is more reduced.
Causes of restrictive lung disease
RA, AS, smoking, scleroderma, bleomycin, chest wall problems.
How does the FRC differ in emphysema and fiborosis?
In emphysema there is elevated FRC due to air trapping. In fibrosis the scarred down lung tissue results in reduced FRC. You can only meausre this by helium dilution techniques.
IgE mediated hypersensitivity when two IgE molecules are cross linekd and attached to a mast cell resulting in immediate anaphylasix.
Type 1 hypersensitivity reaction.
What type of hypersensitivity reaction is Rh disease of the newborn or hemolytic anemia.
Type 2 hypersensitivity whihch is due to IgG or IgM which is preformed after exposures.
This form of hpersensitivity reaction is due to immune complexes which activate complement and inflammation.
example is Arthus reaction after vaccinations or serum sickness.
Cell mediated immunity which requires multiple exposures such as poison ivy and contact dermatitis is what kind of reaction?
type 4 hypersensitivity which is cell meditaed.
high ANCA, GN, normal serum complement, nosebleeds, hearing loss, conjunctitis, coin lesions in lung, arthritis, rash.
Wegners small vessel vasculitis
<eltzers triad of palpable purpura, myalgias and arthralgias + likely Hep C or Multiple myeloma
cryoglobulinemia
tachycardia, tachypnea, cough and CP
PE
majoeelectrocyte disorder in DKA
hypokalemia
PDA connects the ?
pulm arteries to the aorta
Exudate or transudate?
clear, low protein, no cells, very high albumen compared to blood, glucose/serum glucose level is low <0.8
Transudate. High protein (albumen, low sugar)
Transudate or exudate?
cloudy, cells, high protein due to cells but albumen is low, fluidprotein/serum proetin is high and fluid glucose/serum glucose is high > 0.8
High protein and high glucose in Exudate. Light's criteria.
Patient became mute after witnessing a murder is an example of _____
conversion disorder, the stress of the event was converted into a physical ailment.
Hyperbilirubinemia which is mostly conjugated indicates the stone is where?
Stone is most likely in the cystic duct, if it blocks the liver in the CBD you don't see the conjugated bilirubin and if the alk phos is not elevated it is less likely to be obstructing the pancreas.
An AA male from Greece has his urine stain with hemosiderin blue after getting an antibiotic. Why?
He has glucose 6 phosphatse deficency (oxidative injury to RBC) Culprits are sulfa drugs, antimalarials and nitrofurantoin.
3 conditions where you see pulses paradoxis (drop in SBP with inspiration > 12)
cardiac tamponade, tension pneumothorax and asthma.
What vaccinations are required by kids (4yo) going into kindergarten?
4 doses of pneumococcal, 4 doses polio, 2 doses MMR, 1 dose varicella, 2 doses Hep A, 5 doseses DTaP and 4 doses HiB
2 causes of first degree heart block with prolonged PR interval.
Digitalis and increased vagal tone.
How does NTG releave anginal pain in patients with athrosclerosis hint it's not by increasing coronary blood flow (only shown in healthy hearts).
NTG increaseses teh size of capacitance vessels (aka veins are dilated more then arteries) which reduces pooling of blood in heart vessels.
Treatment of pulseless electrical activity (pt has no pulse but EKG shows rhythm)
start CPR and give ACLS drugs ie epi, atropine and vasopressin
If a patient is in V fib or V tach do you give ACLS drugs or shock them
Shock them. Give ACLS drugs in PEA.
Treatment of lone A fib when patient has no other health problems.
Only an aspirin. If there are any other comorbidities ie DM, HTN, HF, TIA, age >75 start warfarin.
Patient diagnosed with pharyngitis who gets ampicillin or amoxicillin and develops a rash has?
EBV. Not strep.
MOA of Metoclopramide
Antiemetic which enhances gastric emptyig due to its promotility effects as a dopamine antagonist.
Autosomal dominant condition of hemangioblastomas in the cerebellum, spinal cord, kidney and retina. Associated with renal cell carcinoma and pheochromocytoma?
Von Hippel Lindau Syndrome. Mutation of the tumor supressor gene.
5 parts of Tetralogy of Fallot
1. pulmonic stenosis
2. overriding aorta
3 VSD- pansystolic murmur loudest at LLSB
4. Right ventricular hypertrophy
5. ASD- fixed wide S2
Most common bloody diarrhea at institutional settings ie nursing home or daycare
Shigella
Diarrhea from undercooked pork
Yersiniosis
Most common infectious diarrhea from poultry.
Campylobacter
Most common bloody diarrhea due to seafood
Vibrio parahaemolyticus
Do you want CT with or without contrast to look for a brain bleed?
Without contrast CT for bleed
stroke that affects lower extremities more then upper extremities motor and sensory affected what artery?
anterior cerebral artery.
What does a stroke of the middle cerebral artery effect?
upper limb defects in motor and sensation > lower extremity. If left frontal lobe is aphasia, right frontal lobe is neglect.
Stroke causing visual hallucinations, alexia, sensory symptoms (thalamus) 3rd nerve palsy with paralysis of vertical gaze, motor defects.
STroke in posterior cerebral artery.
Disease presents with recurrent lymphadenitis, hepatic abscesses, osteomyelitis with catalase positive organisms. What test and what is defect.
Test with nitroblue erazolium to see the phagocytic cell defect in NADPH oxidative burst in Chronic Granulomatous Disease (catalase positive organisms include Serratia, Klebsiella, Aspergillus)
Where does herpes encephalitis most often hit?
The temporal lobes causing seizures and pesonality changs.
Patient has used cocaine and presents with renal tubular necrosis due to myoglobinurea. What test do you want?
CK. it will be highly elevated >20,000 in Rhabdomyolysis.
Most likely cause of amarosis fugax.
This monocular and transient curtain descending loss of sight is most often caused from emboli from the isilateral carotid artery.
Complete painless loss of vision in one eye with optic disk showing venous dilation and disk swelling , retinal hemorrhages and cotton wool spots.
Central retinal artery cclusion.
A patient with diabetic eye disease presents with sudden loss of vision and onset of floaters due to?
vitreous hemorhage
Elevated ESR > 50 yo, stiffness in shoulders and hips, this disorder is related to what other condition.
Polymyalgia rheumatica (key elevated ESR) also relatedto temporal arteritis (related to gialnt cell diseases)
Your patient has an occipital headache associated with vomiting, gait ataxia, no sensory or motor abnormalities, associated with eye muscle dystonia aka blepherospasm, and conjugate deviation of gaze (due to 6th nerve palsy of LR)
consider cerebellar hemorrhege, neurologic recovery is usually complete after surgcial evacuation of the hematoma... it evolves slowly over a few hours and is more common in patients wiht HTN
Acute onset of vertigo and nystagmus without any other neurological defects.
vestibular neuronitis
vertigo, tinnitus and hearing loss which is progressive and unilateral. Associated with migranes.
Meniere's disease which is due to endolymph fluid excess causing labrinthine dysfunction causes (vertigo, tinnitus, hearing loss)
a hypoechoic mass on ultrasound vs hyperechoic mass (compare in terms of breast masses)
hypoechoic mass more likely cyst or fat while hyperechoic mass is firm lesion.
At what time point should you emergently deliver a fetus whose mother is suffering from HELLP?
at 34 weeks gestaion deliver!
What are the positive and negative features of schizophrenia
+ are auditory hallucinations, delusions, disorganized speech and behavior. - features are flat affect, poverty of speech, apathy, a-sociality- inattention.
Patient just returned from Southwest US ie Arizona or TX and has a cough and dypsnea.
Soil born organism Coccidiomycosis . Will show Miliary pattern on CXR.
This Latan American parasite is associated with cardiac disease and megacolon/megaesophagus
Chagas! Due to Tympanosoma Cruzi = protozoa.
3 ways to protect kidneys from contrast
hydration
isotonic bicarbonate
acetylcysteine.
This type of stroke is more common in people with HTN and diabetes. OFten CT is clean but ht epatient is uffering from either pure motor or pure sensory dysfunction (due to injury to the internal capsule)
Consider Lacunar strokes due to microatheroma and lipohyalinosis of the smal penetrating arteries of the brain.
Taking a MAOI such as phenelzine with foods such as tyramine (cheese or wine) can cause
hypertensive crisis.
weak interosseus muscles, hypothenar eminance, (Klumpke's palsy). Injury due to upward pulling of the arm is to what part of the brachial plexus?
C8-T1 = ulnar nerve.
Best test to look at hyperaldosteronism (HTN and hypokalemia)
Aldosteorne to renin ratio is high.
Treatment of uterine atony? 1-3
1. uterine massage
2. oxytocin to increase contraction of myometrial fibers and retract myometrial blood vessels
3. emergent hysterectomy.
Lich nodules on teh iris, bony lesions, axillary freckels and cafe au lait spots.
NF Type 1 (type 2 associated with acoustic neuromas)
Port wine stain on trigeminal nerve distribution, seizures, hemiparesis, angiomatous malformations of the brain
Sturge Weber Syndrome
Ash leaf hypo pigmented spots, cardiac rhabdomyomas, kidney angioleiomyomas, retardation, seizures
Tuberous Sclerosis.
treatment for hepatic cholestasis of pregnancy with normal GGTP, negative viral serologies although LFTs may be elevated.
give ursodeoxycholic acid to promote bile flow.
What 3 things cause elevated alk phos?
placenta, liver and bone.
this case of jaundice is associated with ulcerative colitis, RUQ pain, more common in males, associated with ANCA and increases risk of cholangiocarcinoma.
Primary Sclerosisng Cholangitis (ANCA positive male ulcerative colitis)
This cause of jaundice presents with pruritis, more common in females, elevated alk phos nad cholesterol, no association with IBD, more common in females and associated with ANA And AMA antibodies.
Primary biliary cirrhosis (biliary = boobs more common in females) AMA, ANA)
Risk factors for avascular necrosis of the hip are (name 3). You may not always see changes on XR, need MRI. Sometimes there is no pain on palpation or movement of the limb.
Risk of avascular necrosis is increased sith sickle cell disesae, chronic steroids, alcoholism and hemoglobinopathies (anything that causes irregular sickling and immunosupression)
Patient presents with multiple misscarriages, prolonged PTT but clotting not bleeding, She has Lupus and the Russell viper venom test is prolonged.
Consider antiphospholipid antibody syndrome. This procoagulable state causes a paradoxical prolongation of PTT by IgM or IgG antibodies but actually results in DVTs or PE as well as miscarriages.
Treatment of absence seizures when you can't use ethosuximide
Valproic acid (also used for bipolar)
Patient presents with GN (RBC casts) 10 days after pharyngitis or 20 days after impetigo. What are the serum complement levels?
Post streptococcal glomerular nephritis presents with LOW serum complement
Glomerular nephritis presenting 5 days after pharyngitis caused by IgA nephrology have what effect on complement?
Serum complement in IgA nephropathy is normal while in post strep GN the time course is 10-20 days after infection and complement is LOW
What is your BP goal for patients with Diabetes?
SBP < 130 is more protective
What is the difference between a cohort study and a case control study?
cohort studies look for certain risk factors and classify patients as exposed or not exposed and then follow them to seeif they get the disese. In a case control study the subjects are classified as either having the disease ie case or not ie control and then their chart is analyzed to look for past exposures.
Causes of microcytic anemia (name 3)
iron deficency (TIBC high, serum ferritin and serum iron level are low)
Anemia of chronic disese (low TIBC, normal or increased ferritin- defective utilization of stores)
Reduced globin production as in thalassemias or lead poisioning.
Uremia, thrombocytopemia and hemolytic anemia due to e coli toxin destroying colonic lining causing bloody diarrhea and red cell hemolysis causing jaundice in young children < 4 yo. Chief complaint usually abdominal pain, diarrhea, jaundice, hemolysis, renal insufficency.
Hemolytic uremic syndrome (triad or uremia, thrombocytopenia, and hemolytic anemia) + abdominal pain and diarrhea in children.
Male child age < 10 presenting with low serum antibodies, low B cell number, pyogenic pus forming infections with bacteria such as S. pneumoniae and H. flu
Bruton's Agammaglobulinemia (S linked). Look for recurrent pyogenic infections with incapsulated bugs and low Ab and low B cell number.
Similar presentation to Bruton's but patients are > 15 yo and present with recurrent bacterial infections.
Common variable immunodeficency.
Recurrent fungal and bacterial infections with absent thymus, abnormal T , B , and NK cells. Lymphopenia and early presentation < 1 yo.
SCID
Lymphadenitis, skin absesses, liver absesses, defect of phagocytic cells.
Chronic Granulomatous Disease. Do Nitro Blue Tetrazolium test.
Patient presents with eczema, thrombocytopenia and recurrent encapsulated bacterial infections (mengingococcemia, H flue and S. pneumo). Present with bleeding , ie bloody stools, and low IgM due to dysfunctional T cells as well as platelets.
Wiscott Aldrich Syndrome (x linked recessive). Triad of eczema, thrombocytopenia and bacterial infections.
Best way to increase FRC in post op patients?
raise the head of the bed, the pat takes deeper breaths and more lung used so FRC increases.
You have an alcoholi cpatient with low K and you replete but it doesn't budge. What are you missing.
Concomitant hypomagnesemia, Mg is a cofactor needed for K uptake.
In addition to MONA what other drugs do you consider in MI
give BB to reduce risk of next MI
Heparin if there is cardiac thrombus, CHF or dyskinetic ventricle
ACE I if there is CHF with low EF < 40%
Contrast angina with MI presentation
NTG stops the pain of angina but doesn't touch the pain of an MI. Pain with angina lasts < 2o minutes but remains with MI. ST segment depression with angina will resolve when pain is under control while with MI it is perminant.
What do you give the patient who transitioned from stable to unstable angina?
LMW Heparin for anticoagulation and consider cath lab.
Patient presents with diffuse ST segment elevation, elevated ESR, recent URI and now low grade fever. pericardial rub. What is the most common cause
Coxsackie virus is most common cause of pericarditis followed bith malignancy, autoimmune diseases TB and uremia.
Treatment of DVT
start on heparin with gradual cross over to warfarin. Maintain on warfarin for 3-6 months min.
Contrast vWF deficency with hemophilias.
vWF is AD and it prolongs bleeding time and PTT both. Hemophilias only prolong PTT and are X linked.
How does liver disease affect coagulation?
Liver disease has elevated PT with +/- PTT. All factors are low.
What do you use to follow heparin vs warfarin vs aspirin?
heparin- follow intrinsic PTT path... reverse wtih FFP.
warfarin- follow extrincic PT pathway.
aspirin affects bleeding time (uremia also deactivates platelets)- reverse with platelet transfusion
A patient has a BNP of 300 + signs of heart failure. Can you rule it in or out?
BNP < 100 rule out HF
BNP > 500 rule it in.
If between you can't say
Name 3 signs of right sided heart failure.
dypsnea, peripheral edema, pulmonary congestion, elevated JVD, heaptomegaly, ascites.
3 causes of cor pulmonale
Cor pulmonale is R ventricular enlargement due to PE, primary pulmonary HTN (young female), or COPD or even sleep apnea.
3 causes of restrictive cardiomyopathy
amyloidosis, sarcoidosis, hemochromatosis, myocardial fibroelastosis. Listen for pericardial rub and surgically remove pericardium.
Treatment of frequent PVCs assuming patient not in HF.
Give lidocaine.
You notice a delta wave on EKG, you want to treat with procainamide or quinidine as antiarrhythmics and want to avoid AV block with what 2 meds.
Avoid CCB ie verapamil and Digoxin
Treatment of HOCM, what meds do you aovid.
Treat HOCM with BB to allow time to fill. Avoid positive ionotrops, diuretics and vasodilators.
At what location is fetal oxygen the highest
Most oxygen at the fetal vein coming in, the two fetal arteries in the cord are deoxygenated blood.
Murmur of PDA?
continuous machine like murmur at the upper left sternal border. If not needed close with NSAID
3 indications to intubate
ph < 7.3
O2 <50
CO2 >50
FEV1/FVC ratio in obstructive lung disease like COPD or asthma
low. FEV1/FVC < 0.7 in obstruction. Normal or elevated in restrictive diseases although both may have decreased FEV1.
You note prolonged expiratory phase indicating loss of lung elasticity as well as pursed lip breathing in a patient with decreased heart and breath sounds and scattered rhonchi. What is the treatment?
Treat emphysema with smoking cessation, bronchodilator, anticholinergic like ipratropium and immunizations as well as Corticosteroids for acute exacerbations.
Wheezing in young children < 2 in winter.
RSV.
Young patient with solitary pulmonary nodule (no old films), has not been in caves (histo), has not been to the SW (Coccidiomycosis), not a smoker, not immigrant (TB).
Consider hamartoma. a disorganized overgrowth of local tissue that is not malignant in origin and that doesn't grow any faster then normal tissue. Get serial XR.
PNA in college student (2)... which one is it if there are sexually active vs there are cold agglutinins
Cold agglutinins are mycoplasma
Chlamydia other common cause in college aged students.
Current jelly sputum in alcoholic with dypsnea
Klebsiella... also be concerned about s aureus and anaerobes from aspiration in alcoholic.
2 main causes of pna in CF
s. aureus and pseudomonas@
PAtient is a metal or pottery worker who is also an immigrant with cavitary lesions and recent fever and cough.
Consider aspergillus infection of TB lesions.
Patient with long smoking hisotry suddently with fever and cough. 2 most likely causes of PNA
moraxella or H flu in COPD
2 main causes of dypsnea when exposed to bird droppings
if immunosupressed think crptococcus, otherwise think histoplasmosis if in ohio missippi river valley or exploring caves (bats)
Child with dypsnea aged 2-5 vs age < 2. What different viruses
Child < 2 think RSV
Child 2-5 think parainfluenza virus causing croup or epiglottis.
What ulcer ihas less pain with eating.
Duodenal ulcer's pain is releaved by eating.
Severe or atypical ulcer presentation, resistant to teatment. What test do you get?
Get gastrin levels to look for Zollinger Elison syndrome
Tripple therapy for h. pylori
amoxicillin, clarithromycin and PPI
Camping trip, comes home with fatty, greasy malodorous stools tha tfloat. Treatment
Treatment of Giardia is with Flagyl aka metronidazole.
Patient has thrombocytopenia, renal failure and hemolytic anemia after having diarrhea ( e coli or shigella) what is the treatment?
Hemolytic uremic syndromed with renal failure, thrombocytopenia and hemolytic anemia just need supportive treatment.
IBD with cobblestoning, transmural skip lesions from mouth to anus, surgery worsens it
Chron's Disease
This IBD affects the rectus mostly and spares the anus, causes bloody diarrhea, only affects mucosa and submucosa, increases risk of colon cancer, toxic megacolon, pseudopolyps, and is associated with primary sclerosisng cholangigits. Surgery is usually curative.
ulcerative colitis.
Treatment of Hep B when you have high E marker of infectivity
Treat with IFN alpha and Ribavirin to slow liver damage and progression.
Note you can only get Hep D with Hep B infection.
Hepatitis in a woman < 40 yo, with anti smooth muscle or ANA Ab is treated with?
This is idiopathic autoimmune hepatitis and is treated with steroids.
Why does liver disease often cause hypoglycemia
liver stores glycogena nd in liver disease glycogen stores are down.
Nonsmoker with liver disease and emphysema
Autosomal recessive alpha 1 antitrypsin deficency.
you have a male patient with arthritis, impotence, dilated cardiomyopathy, bronze diabetes and cirrhosis, what type of inheritance is it?
Hemochromatosis is autosomal recessive and is more common to benoted in males as they dont' menstruate
Autosomal recessive disease where the serum ceruloplasm is low, urinary copper excretion is high. You note copper in the basal ganglia causing psychosis. What is treatment?
Wilson's disease is autosomal recessive and is treated with penicillamine copper chelator.
2 causes of unconjugated hyper bilirubinemia
Gilber's and Hemolysis both cause increases in unconjugated bilirubin. While hepatobiliary disease is usually sa cause of conjugated hyper bili.
Clay colored stools, dark urine, hyperbilirubinemia that is conjugated.
Think hepatobiliary disease.
A patient has esophageal dysmotility and Raynaud's ... what Ab do you look for and what otehr associated conditions are there
CREST- calcinosis, Raynauds, Esoph dismotility, Sclerodactyly, telangectasias
Look for anticentromere antibody and positive ANA
Scleroderma antibody?
Anti-topoisomerase antibody is positive in scleroderma.
2 main causes of pancreatitis
alcohol and gallstones.
< 2 years old with bilious vomit, currant jelly stools, belly pain, saussage shapped mass palpated. What do you do?
Get contrast air enema for intrasusception.
2 GI disorders seen with CF
rectal prolapse and meconium ileus.
Is omphalocele or gastroschisis assoicated with other syndromes of development?
Omphalocele (intestines in sac) also associated with OTHER developmental abnormalities.
Abdominal pain, arthritis, rash and hematuria/proteinurea. IgA antibodies are found on biopsy.
Think Henosch Schonlein purpura. Consider HSP in cases or URI, rash on LE and buttocks that is purple, hematuria, proteinurea, GI bleeding, pain. Due to IgA antibodies in skin and kidney.
At what level do you treat neonatal jaundice?
If unconjugated bili is > 15 treat with lights. Peaks at 3-5 days.
Severe unconjugated hyperbilirubinemia is caused by?
Crigler Najjar causes severe unconjugated hyperbilirubinemia. Mild hyperbilirubinemia is caused by Gilber's or by hemolytic anemia.
Treatment of sub acute thyroiditis (hypothyroidism) with diffuely tender thryoid gland after viral infection.
Treat wiht NSAID self limiting.- Similar to sick euthryuroid syndrome with decreased T4 but normal TSH. Self limiting.
Patient presents with pretibial myxedema, what is the treatment?
See pretibial myxedema with Graves treat with radioactive iodine.
Patient presents with skin pigmentation, weight loss, n/v, dizzy, syncopy, hyponatremia and hyperkalemia. How do you determine cause and what do you treat wtih.
Treat adrenal insufficency with steroids. Determine if primary (addison's due to adrenal underproduction) or due to pituitayr underproduction of ACTH (no skin hyperpigmentation)
Primary test for Cushing's?
Test 24 hour urine for cortisole. Then do dexamethasone supression test to look for entral vs peripheral caue.
What is the treatment of nephrogenic DI?
Treat nephrogenic DI (no ADH reaction in the kidney) treat with THIAZIDE diuretics.
Definition of ARF
elevated BUN (>18 abnormal) and Cr, metabolic acidosis (low HCO3) due to inability of kidney to secrete H ions, hyperfvolemia, hyperkalemia.
Patient with RF, > 40 yo, epitaxis, hemoptysis and high ANCA titer
Wegner's granulomatosis- treat with cyclophosphamide immunosupressant.
Name 3 nephrotoxic drugs
Cisplatin, cyclosporine, aminogycosides ie gentamycin, methicillin, NSAIDS
Indications for emergent dialysis
uremic encephalopathy
pericarditis/ HF
pH < 7.25
Hyperkalemia and arrhythmias.
Most common cause of nephrotic syndrome protein > 3.5g/d in children and in adults.
In children nephrotic syndrome is usually due to minimal change disease with podocyte in jury. In adults suspect Diabetes (iother causes include hepatitis, amyloid, lupus, drugs ie gold and captopril)
3 top causes of renal failure
Diabetes, HTN, PCKD
How does Chronic RF affect Ca
Results in hypocalcemia and hyperphosphatemia due to imapired vit D production. Give phosphate binders ie calcium carbonate
Compare radiological findings between RA and OA
in OA note joint space narrowing and osteophyte bone spurs. While in RA there is a pannus of articular cartilage.
Compare bireference in gout vs pseudogout?
Gout- Negative birefringence. Use colchicine an dNSAIDS tfor acute attacks and Allopurinol for long term maintenance therapy.
Pseudo cout more often knees and elbows and note positive birefringence due to calcium pyrophosphate cyrstas.
Can't see, pee or climb or a tree. Urethritis is due to Chlamydia, associated with HLA B27.
Reiter's Syndrome.
Treatment for Lyme disease with migratory rash? What if pregnant?
Give doxycycline for Lyme's . If pregnant give Amoxicillin.
Migratory polyarteritis with fever following strep pharyngitis is
Rheumatic fever.
Slipped capital femoral epiphysis is confirmed by XR?
Legg Calve Perthes Disease
Contrast Osgood Schlatter with Legg Calve Perthes Disease?
Osgood Schlatter is osteochondritis aka inflammation of the bone at the tibial tubercle (young boy 10-15 yo) with tenderness at the knee. In Legg Calve Perthes there isa slipped femoral epiphysis requiring surgery not just NSAIDs and rest.
Heliotrope rash, proximal muscle weakness, calcium deposits in tissue seen in XR. Often autoimune or due to malignancy. Can be associated with EBV and Lupus and you note a high CK.
Dermatomyositis.
Young child <5 with truncal rash which spreads to hands and feet, very red eyes, lymphadenopathy, fever, strawberry tongue. What is the treatment
Kawasaki's diseaes treat with Aspirin and IV IG
This disease is due to immune complex deposits in medium sized vessels. IT is associated with high ESR, abdominal pain, RF, neuropathy as well as anemia, leukocytosis and infection with hep B or cryoglobulinemia.
Polyarteris Nodosa- think of RF, abdoinal pain, and neruological problems. Type III hypersensitivity.
Pulseless disease in young asian females?
Takaysaus' arteritis. Affects large vessels so when aortic arch is affected one arm may only have faint pulse. Treat with steroids.
Nosebleeds + hemoptysis/dypsnea + RF =
Wegner's disease
Patient with rapidly growing hat size, hearing problems, bone pain, paraplegia, high alk phos, normal Ca and normal phosphorous.
Pagets disease , watch for increased risk of osteosarcoma.
2 diseases that show Target cells on smear
Thalassemia or liver disese
TIBC and iron are both low, ratio is normal. Serum ferritin is elevated. MCV < 80. Do you give iron?
This is anemia of chronic disese and ferritin is elevated because it is an acute phase reactant. Don't give Iron. Treat the underlying disease.
Causes of and presenting signs of B 12 deficency.
B12 deficency is a microcytic anemia MCV < 80. May be due to antiparietal cell antibodies, or anti IF antibodies, low Gastrin levels which result in achlorhydia and low absorption, may be due to vegan diet, pancreatitis or fish tapeworm (diphyllobothrium latum). Shilling's test can help.
At what value to you give platelets if a patient is asymptomatic.
AT 10,000. Higher if bleeding.
If you patient has DIC or vWF what do you give them to stop bleeding?
Give cryoprecipitate which contains both fibrinogen for clotting and factor VIII.
Why does vWF have both a prolonged PTT and bleeding time?
dysfunctional platelets and dysfuncitonal factor VIII give cryoprecipitate.
Which pathway does warfarin affect?
Warfarin affects vitamin K factor s including 2,7,9, 10 all inthe extrinsic PT pathway.
After a viral infection patient starts making antibodies against platelets.
Idiopathic thrombocytopenic purpura. Treat with splenectomy.
Young adult with low RBC due to hemolysis, low platelets, renal failure, fever, jaundice, thrombocytopenia causing petechial rash.
Thrombocytic Thrombocytopenic Purpura is an autoimmune disease where antibodies are made against RBC and platelets. Treat with plasmaphoresis. Don't give platelets as the Ab make them hypercoagulablel.
This type of leukemia is seen in young children <5 yo, associated with Down's, positive periodic acid Schiff (PAS +),presentation is with fever, bleeding, pancytopenia, anemia.
ALL = young children, acute, All leukemias have anemia, fever, pencytopenia
Leukemia seen in adults >30 not children, DIC, AUER rods, pancytopenia, bleeding, fever.
AML = aur rods. Peroxicase positve granuels in myeloblasts.
Middle aged person presenting with high # WBC >50,000, splenomegaly, philadelphia chromosome.
CML = philadelphia chromosome, middle aged, leukocyosis.
Old person presenting with SMUDGE cells and lymphadenopathy. Most common leukemia
CLL = old patient, SMUDGE cells.
Stary sky cytology, assoc with EBV in africa, neoplasm of B cells with high mitotic index with a mass on abdominal viscera.
Burkitt's lymphoma.
Reed steinberg cells with owl eye
Hodgkin's disese (young pt <30.
Patient >40yo, Bence Jones proteins, high Calcium, IgM spike
Multiple Myeloma
parathyroid, pituitary and pancreas
MEN I
thyroid (medullary) parathyroid and pheochromocytoma
MEMN IIa
thyroid (medullary) pheochromocytoma and mucosal neuroma
MEN IIb
familial polyposis (CC risk) and soft tissue tumors
Gardener's syndrome.
freckles around mouth, GI polyps, non colon cancer risk
Peutz Jegher's.
seizures, retardation, renal angiomyolipomas, cardiac rhabdomyomas, ash leaf spots.
Tuberous Sclerosis
increased risk of leukemia (ALL)
Down's and NF
NF 1 also increases risk of bone cysts, Wilm's tuor and Neurofibromas.
Your patient has small cell lung cancer. Treatment with surgery or chemo or radiation?
Always start chemotherapy. Early mets with SCLC.
Unopposed estrogen incresaes the risk
of endometrial cancer.
alpha fetoprotein is a tumor marker for
testicular and liver cancer.
SIADH and hypercalcemia due to elevated PTH like hormone makes you concerned for what type of cancer
Small cell cancer is associated with SIADH and hypercalcemia
Most common cause of breast cancer?
Invasive ductal carcinoma usually in older women. Check if Her2 neu positive as you can treat with trastuzumab antibody therapy.
What meds can you treat with in progesterone sensitive breast cancer.
SERMs like tamoxifen or letrozole.
Hormonal treatment for prostate cancer mets?
Second most fatal cancer in males. Treat with leuprolide a GnRH agonist or androgen receptor antagonist flutamide if there are mets.
If you had a recurrence of colon cancer with mets to the liver what tumor marker would you look for?
Look for carcinoembryonic antigen as it is assoiated with coon cancer. Adjuvant chemo with 5FU often used with mets.
Most types of pancreatic cancer with epigastric pain, migriatory thrombophlebitis (Trosseau's syndrome of hypercoagulability), cholestatic symptoms.... due to
Adenocarcinoma (ductal epithelium)
Also see insulinoma which is a beta cell tumor which causes LOC or stupor. Cehck glucose levels and if they are hypoglycemic with high C peptide then suspect insulinoma.
This common cause of ovarian cancer shows psammoma bodies on histology and is more common in older women who have never used OCP.
Serous cystadenocarcinoma is most common cause of ovarian cancer. OCP are protective for ovariana nd endometrial cancers.
This tumor causes precocious puberty in girls while this tumor causes precocious puberty in boys or virilization.
Granulosa cell tumor- estrogen producitng
Leydig or Sertoli tumor causes virilization due to testosterone.
This cancer sends mets to the ovaries and looks like a ring.
Krukenberg tumor is a stomach cancer which sends mets to the ovaries.
Most common brain tumor in children, most common in adults.
Children- infratentoral tumors ie cerebellar astrocytomas and ependymomas.
Adults get gliomas which are often intraparenchymal astrocytomas or meningiomas with calcifications.
Most common brain tumors in kids 3
cerebellar astrocytomas, meduloblastomas and ependymomas
Most common brain tumors in adults 2
if calcified think meningiomas
if not calcified think intraparenchymal astrocytomas (gliomas)
If you find a hemangioblastoma what disorder are you thinking
Von Hippel Linday Syndrome is associated with angioblastomas, renal cell carcinoma and pheochromocytomas due to tumor supressor gene mutation.
Calcified tumor around the sella tursica interfering with a child's sight?
Think of craniopharyngioma
Lung carcinoids are common but do not present with the diarrhea, flushing, cramps seen with other carcinoid tumors, why?
Carcinoid syndrome is only seen when the tumor has mets in the liver, otherwise these usually GI or lung tumors breakdown products of seronin are cleared by the liver befroe they enter the bloodstream.
Type of bladder cancer seen with vinyl cloride exposure, painless hematurea
Angiosarcoma.
What cancer is associated with EBV in children
Nasopharyngeal cancer is associated with children with EBV infection.
The risk of cholangiosarcoma increases with what type of IBD?
With ulcerative colitis cholangiosarcoma risk increases
Sunburst pattern on XR of lower extremity, boy < 30 yo.
osteosarcoma = sunburst bone pattern.
Incidental finding in young child , unilateral flank mass
Wilm's tumor.
This neural crest cell is often calcified and arising from the adrenal gland children < 2 yo.
Neuroblastomas. Think NF1
Where does testicular cancer travel to?
retroperitoneal lymph nodes
What is Wipple's Disease?
malabsorptive steatorrhea, migratory arthritis, lymphadenopathy, weight loss, fever. Due to bacteria R. whippelii.
arthritis + diarrhea + weight loss=
arthritis + conjunctivitis and urethritis =
Wipples
Reiter's
Patient presents with weight loss. They have a migratory rash, diarrhea and hyperglycemia.
Think glucagonoma cancer of the pancreas.
Papillary breast cancer presents with?
Nipple discharge and breast mass
Pagets disease of the breast presents with?
scaly itchy rash around the nipple and usually an underlying adenocarcinoma. PAthology shows large halos aorund cell nuclei
How do you differentiate between a rotator cuff tear and rotator cuff impingement?
Inject lidocaine. In cases of tendonitis and impingement there will be improvement when if there is a tear there will be no change. Caused by repetative movements over the head ie tennis.
Frozen shoulder is aka
Adhesive capsulitis, can't move arm above teh head
Why does polycythemia vera often cause gout?
Myeloproliferative disorders incresae uric acid levels, therefore very high rBC count also often means painful joint.
Grout, behavioral problems and self injury, mental retardation, neurological dysfunction.
Lesch Nyhan Syndrome due to HPRT deficency. Overproduction of uric acid.
How do you increase fetal hemoglobin levels in patients with sickle cell disease?
Hydroxyurea increaes fetal hemoglobin levels.
Heinz bodies (hemoglobin specks in teh RBC showing up on peripheral smear) indicate this type of hemolytic anemia.
G6PD deficency.
A patient who is asplenic may have Howel Jolly Bodies on peripheral smear, why?
Howell Jolly Bodies are nuclear remnants in RBCs which are usually cleared by the spleen. These small round blue inclusions on Wright Stein are seen in patients that are functionally asplenic.
What is a schistocyte?
Schistocytes are injured fragments of RBCs seen in hemolytic anemias.
Risks of methotrexate (DMARD- disease modifying anti rheumatic drug)
macrocytic anemia (inhibiton of folate), also why methotrexate is bad in pregnancy, causes stomatitis, alopecia, ILD, hepatitis, fever.
Where is the location of De Quervain tenosynovitis
At the base of the thumb.
This organism causes PID and is a gram positive organism with sulfur granules
Actinomyces causes PID bit is G +
What stain do you use for cat scratch disease and PCP?
Silver stain.
Parrot pneumoniae
Chlamydia psittaci
BActeria often transmitted by animal bites? How about specifically cat scratch?
Pasteurella molticida cellulitis causer from pet bites while Brucella is cat bites/scratch disease.
Treatment for patchy XR showing pneumonia in college kid, xr looks really bad btu patient feels ok.
Give azithromycin or other macrolide for mycoplasma. Test is for cold agglutinin antibodies.
What pneumonia presents similar to mycoplasma but has negative agglutinin antibodies?
Chlamydia pneumoniae. No cold agglutin antibodies.
When is s. aureus pna seen?
In IV drug users or aptients with CF (although pseudomonas is more common) or hospital acquired.
Treatment of Klibesella, pseudomonas or H influenzae is?
Amoxicillin or Ampicillin.
Treatment for simple strep pneumoniae?
cephalosporin ie cefotetan or other 3rd generation.
Treatment for PCP PNA
BActrim or if sulf allergic pentamidine.
This test will show multinucleated giant cells in patients with varicella.
Tzanck smear.
This common disease in children is due to parvo B 19. It presents with a slapped cheek rash which proceedes to arms and legs. Child is feverish and tired.
Erythema infectiosusm 5th Disease
Koplik (blue ) spots on mucosa, fever, rash on head and neck moving down, conjunctivitis, runny nose and cough.
Measles (Rubeolla) = koplik spots
Tick bite on east coast, fever, HA, malaise, rash on wrists and ankles. Can cause DIC and delerium. Treatment?
Treat Rocky Mountain Spotted Fever with doxycycline.
Children < 3 yo, rash on chest and abdomen, high fever, due to Herpes Virus type 6.
Roseola infantum.
Sandpaper rash on trunk and abdomen, fever, rash stops when fever stops, strawberry tongue
Scarlet fever
prophylactic coverage for contacts of people exposed to Neisseria meningitis
Ciprofloxacin, Ceftriaxone or rifampin.
Bronchiolitis young children with wheezing, hyperinflamtion, crackes, due to RSF or parainfluenza. Treatment?
Give ribivaran for RSV coverage.
What virus casues Croup?
Parainfluenza. URI, barking cough, stridor, steeple sign of sub glottin narrowing. Give ist tent and racemic epinephrine.
Cause of epiglottitis?
Due to H influenzae. Children <5yo, high feve,r toxic, drooling, thumb sign. Don't hesitate to intubate.
Treatment of Strep B aka strep Agalactiae
Causes meningitis in neonates. Treat mom with Amoxicillin or Ampicillin.
LAD, exudative tonsilitis, fever, sore throat, absent cough!
Strep pyogenes pharyngitis.
What is erysipelas
Superficial shiny red tender cellulitis.
Treatment of animal bite with suspected Pasturella infection
Ampicillin.
You have a patient who has cellulitis but they are high risk so you don't want to just treat with PCN or Vanco... ie they have serious burns, trauma or diabetes and you're worried about pseudomonas. TX?
Amoxicillin to cover G+ and Aminoglycoside like gent for G- and pseudomonas.
Treatment for Lyme's disease
doxycycline just like for gonorrhea.
Post transplant patients need prophylaxis against?
PCP just like HIV patients they need BActrim and possibly gangcyclovir for CMV prophylasix as well.
Treatment of syphilis?
Penicillin, if allergic give doxycycline.
Baby with rhinorrhea, jaundice, anemia, HSM, lesions on palms and soles of feet.
Congenital Syphilis.
-hand and foot rash, HSM, rhinorrhea
Baby with HSM, choreoretiniitis, intercranial calcificaitons, and hydrocephalus.
Congenital toxoplasmosis. - calcifications, HSM, retinitis
Baby with cataracts, deafness, heart defects, blueberry muffin rash, thrombocytopenic purpura and HSM.
Congenital rubella- deaf, cataracts, heart
Signs of congenital CMV infection
CMV infection causes IUGR, hearing loss, periventricular calcifications, microcephaly, HSM, petechiae.
Two prenatal exposures that cause hearing problems for fetus.
CMV causes hearing loss as well as congenital Rubella.
Two prenatal exposures that cause intercranial calcifications
CMV and toxoplasmosis both cause intercranial calcifications.
Two prenatal exposures that cause vision problems.
Toxoplasmosis causes retinitis. Congenital Rubella causes cataracts.
In this bone marrow disease there is a very low ESR and a low EPO due to neg feedback.
Polycythemia vera has a low EPO as the kideneys are telling teh BM to stop making so many RBC, ESR is also low.
Give an example of contact dermatitis and what type of hypersensitivity reaction is it?
Contact dermatitis is a type 4 cell mediated delayed hypersensitivity reaction to such items as nickel or poision ivy.
Two drug causes and two diseases that cause hirsuitism
Hirsuitism can be caused by minoxidil and phenytoin as well as PCOS and Cushing's.
Treatment for pediculus capitis, corporis or pubis (lice)
permetherin cream.
Two types of fungal infections where you actually give systemic ie oral griseofulvin or fluconazole
tinea unguium (nails) or tinea capitis
purpuritic, purple planar polygonal papules
Lichen planus treated with steroids.
This skin disease results in bullae where there is "unglueing or the epidermis" due to antibodies to desmosomes. Associated with malignancy often on Hodgkins lymphoma.
Pemphigus vulgaris
Herald patch, followed by Christmas tree pattern of rash alon parallel skin clevage lines. Treatment?
Pityriasis rocea. Self limiting about 6 weeks thought to be viral.
silvery, scaling papules and plaques on extensor surfaces.
psoriasis.
Acne of middle age with eyelid inflammaiton aka blepharis and red nose.
Rosacea. Treat with metronidazole or oral tetracycline.
Itchy burrows in the finger web spaces and flexor surface of wrists due to
Scabes = finger web spaces and flexor surfaces. Treat wtih permetherin cream.
Dandruf aka
Seborrheic dermatitis
Recurrent otitis media, eczema and thrombocytopenia. X linked disorder.
Wiskott Aldrich syndrome.
Diffuse telangiectasias, epitxis, AV malformations, Hct is increased due to shunting.
Osler Weber Rendu syndrome of AV malformations.
Old man barnacles hwich appear stuck on and are often greasy, and slow growing
Seborrheic keratosis.
Cutaneous horns, slow growing, hard sand paper like flat areas on aged skin.
Actinic Keratosis
Patient presents with hyperparathyroidism (elevated Ca and low phos) as well as elevated gastrin and multiple GI ulcers. What two disorders are linked? What if he has a pheo or pituitary tumor too...
MEN 1 + Zollinger Ellison Syndrome are linked
Patient with new onset diabetes look for other diseased organ systems.... what if they also have arthralgias, restrictive heart disease, hypogonadism?
rule out Hemochromatosis. Get iron studies first.
Adolescent boy with recurrent nasal obstruction and nosebleeds, can erode into bone.
Juvenile angiofibromas. Refer to ENT for removal. Dangerous to touch as they can exsanguinate.
LP shows mostly neutrophils, low sugar.
Bacterial meningitis.
High lymphocytes in LP
Think viral meningitis.
LP with elevated protein but normal glucose and no cells.
Think Guillian Barre,
LP shows lymphocytes but sugar is Very LOW (normal is 50-100)
Think of TB or fungal infections with lymphocytes and low sugar. Bacterial LP shows high neutrophils. Viral LP shows high lympohcytes.
Signs of LMN lesions
fasiculations, areflexia
What are the temporal lobes responsible for... how about the parietal lobes.
L temporal lobe = Werneckie's aphasia
R temporal lobe = aggression and hypersexuality
L parietal lobe = math, writing
R parietal lobe = hemineglect.
CN III and IV are in ?
the midbrain has CN III and IV
CN V, VI, VII, VIII are in ?
the pons hs CN V, VII, VIII
CN IX, X, XI, xII are in ?
are in cerebellum
resting tremor or chorea as in huntingtons is due to damage to wehre?
Basal ganglia
Hemiballismus is due to damage at?
subthalamic nucleus
facial expression, anterior tongue taste, salivary glands are innervated by
Facial nerve CN VII
Muscles of mastication, facial sensation including the corneal reflex is?
Trigeminal nerve CN V
Drugs that cause damage to CN VIII manifested as tinnitus, deafness, vertigo include
aminoglycosides, loop diuretics, aspirin, cisplatin. More commonly meningitis and not drugs in children.
Damage to the accessory nerve means you can't turn toward or away from the affected side?
Can't turn away from affected side
Children with congenital heart defects are at risk for developing? hint they ahve HA, focal neurologic changes or seizure.
intercranial abscenss. Risk increases with dental infections and head trauma as well.
rash plus muscle weakness in teh setting of malignancy (elevated CK and EMG showing weakness)
Dermatomyositis
Treatment for MS which modulates T cell autoimmunityto myelin.
Glatiramer.
Patietn has axillary nerve injury, paralysis of deltoid and is holding arm in external rotation. Was there an anterior or posterior dislocation.
Anterior dislocation results in external rotation.
Autoimmune hemolytic anemia (caused by drugs like PCN, Sulfa or mehtyldopa), ITP, transfusion reactions, Good pastures, Myasthenia Gravis, Pernicious anemia and transplant rejection are all due to what type of immune hypersnesitivity?
Type 4 cytotoxic response due to preformed IgG and IgM.
Patient with abdominal pain, weight loss and arthritis. Disease is due to antibody complexes (type 3 immune reaction) being deposited in blood vessels causing thrombi and aneurysms.
Polyarteritis Nodosa.
What do you do when HIV pt
CD4 <350
CD4 <200
CD4 <100
CD4 <350 start antiretroviral tx
CD4 <200 start bactrim prophylaxis pt hasAIDS now
CD4 <100 start azithromycin prophylaxis for mycobacterium avium and fluconazol for cryptococcus and candida.
Cause of diarrhea in immunosupressed.
Cryptosporidium.
Recurrent lung and sinus infections in baby around 6 months when mothers antibodies are no longer around
Brutons agammaglobulinemia.
Eczema, thrombocytopenia and respiratory infections.
Wiskott Aldrich Syndrome, x linked.
People with complement deficencies are more likely to get what bacterial infection?
Neisseria
staph aureus and pseudomonas are both catalase positive organisms which are more likely to infect someone with what x linked disorder of NADPH
Chronic Granulomatous Disesae
Albinism with defect in microtubule polymerization affecting neutrophil chemotaxis.
Chediak Higashi.
Recurrent staph infections of the skin, high IgA, high IgE and eczema
Job's syndrome.
Steorid use can present as
hypogonadism, hepatotoxicity, psychological disturbances, cardiac disease, coagulopathy, erythrocytosis, premature epiphyseal fusion and short stature.
new cases / year =
new cases + old cases = total cases =
incidence vs prevalance of a disdease
# positive tests/ all those that have the disease aka ability of the test to detect the disease.
sensitivity, rules in.
# negative test/ all those that don't have the disease, ability to detect absence of the disease
sensitivity , rules out
Define positive predictive value.
PPV is the chance that the person has a positive test result out of all people who have the disease.
Define Negative predictive value
NPV is the chance that a person has a negative test result out of all people who don't have the disease.