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67 Cards in this Set

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Child

irritable, poor attention, lethargic, anorexia, abdominal pain (vague), constipation, pale, reduced reflexes in extremities
Lead poisoning

Inh ALA & Ferrochelatase
Tx with EDTA or chelation therapy
Bloody diarrhea, hx of travel and liver infection
Probably Entamoeba Histolytica

look for "cartwheel" distribution of chromatin in nucleus and injested RBCs on liver biopsy
Rapidly increased serum creatinine, nausea, vomitting, malaise
Acute Renal Failure

(most common cause is pre-renal; i.e. renal hypoperfusion)
Young adult male, Hep B or C positive, multi-organ affliction (espec. GI or Renal), thrombus symptoms, fibrinoid necrosis of vessels with fibrotic thickening in healing vessels
polyarteritis nodosa
50's male, rapidly progressive memory loss, ataxic gait, startle myoclonus, recurrent bursts of high voltage slow waves on EEG
Creutzfeldt-Jakob Disease

Hallmark: Spongiform change in gray matter
Japanese male, sexually active, 25 years later gets lymphadenopathy, hepatosplenomegaly, skin rash, hypercalcemia, elevated WBC
ATLL after HTLV infection
16 y/o with HTN, hypokalemia, increased blood volume, decreased renin, acne, hirsutism
Partial glucocorticoid resistance

Inc. ACTH causes acne/hirsutism, Inc. steroid precursors cause other symptoms
Child is clumsy, frequent falls, knee/ankle injuries, foot drop, pes planus (flat feet), muscle wasting gives legs stork-like appearance
Charcot-Marie-Tooth Disease

Sensory-motor neuropathy type one results in atrophy in ant. compartment of leg (deep peroneal nn)
Tremor, tachycardia, HTN, malaise, nausea, hallucinations, delirium tremens (autonomic instability, fever, tachycardia, delirium, death)
Alcohol withdrawal

tx with benzos or replace the ETOH
Fatigue, malaise, DIC and AML diagnosis...What sub-type
M3 AML subtype (promyelocytic Leukemia), assc with lots of Auer rods
Kid, bright red rash starts on cheeks and spreads to shoulders/upper thorax. Then gets reticulated, lacy appearance.
Parvo B19 (if spread to a preg woman in 1st trimester, baby could get aplastic anemia and develop "Non-immune hydrops"
Flacid bullae with cleavage plan above the basal layer of epidermis
pemphigus vulgaris (aasc with Desmoglein 1 or 3)
Several hours of increasing chest pain thats not relieved by nitroglycerin (no MI findings)
Unstable angina (probably due to thrombosis with or without underlying atherosclerosis)
Slightly curved, motile, gram negative aerobic rods
Pseudomonas aeruginosa (pneumionia and Otitis EXTERNA)
Several hours of increasing chest pain thats not relieved by nitroglycerin (no MI findings)
Unstable angina (probably due to thrombosis with or without underlying atherosclerosis)
Slightly curved, motile, gram negative aerobic rods
Pseudomonas aeruginosa (pneumionia and Otitis EXTERNA)
Infant with hypotonia, progressive dyspnea, fatigue, hepatomegaly, bilateral rales, cardiomegaly
Glycogen storage disease (most likely Pompe's--lysosomal alpha glucosidase deficiency--which includes cardio/hepatomegaly)
Infant with hypotonia, cirrhosis, and early death
Andersen disease (branching enzyme deficiency)
Infant with severe hypoglycemia, lactic acidosis, hepatomegaly, renomegaly, hyperlipidemia, and hyperuricemia
Von Gierke's Disease (Glucose 6 Phosphatase disease)
Infants with muscle cramps and weakness on exercise
McArdle's Disease (myophosphorylase deficiency)
Infants with hepatosplenomegaly, microcephaly, severe mental retardation, zebra body inclusions (characteristic foamy macrophages), early death
Niemann-Pick Disease (Sphingomyelinase deficiency)
Infant born with jaundice and icterus that don't respond to photo therapy (although no kernicterus forms). After phototherapy total bilirubin is sky high, but direct bilirubin is ok
Crigler-Najjar Syndrome (decreased UDP-glucuronyl transferase activity prevents conjugation of bilirubin)
Carotid bruits
Severe atherosclerosis (stroke risk)
66 y/o man with chronic fatigue, lymphadenopathy, hepatosplenomegaly, isolated lymphocytosis, mature lymphocytes
CLL (tx with nitrogen mustard...ie chlorambucil)
65 y/o male with HTN and stroke hx. only shaves right face. Can feel touch on right and left face, but if both are touched simultaneously, he only feels it on the right side
Sensory neglect syndrome (rt parietal lobe defect)
Normal infant at birth can't pass muconium, distended abdomen, vomitting, poor feeding, narrowed rectum. Passes some stool with digital rectal exam.
Hirschsprung disease--neural crest migration defect resulting in congenital constipation from lack of ganglion cells in meissner (submucosal) and auerbach (myenteric) plexi in rectum (always involved). Can extend more proximal as well.
70 y/o female in nursing home with flu-like sx's later develops high fever, dyspnea, and productive cough. Also mental status changes. CXR shows cavitary lesion in left lung
Pulmonary abcess (most likely staph aureus)
Wasting of thenar eminence and lack of sensation on nailbed of middle finger
median nn lesion
80 y/o man in car accident with severe thoracic and abdominal trauma goes to ICU and gets rapid myocardial dysfunction, hypotensin, DIC, and coma
Septic shock (big giveaway is DIC) probably from gram - bacteria spilling out of his bowels
60 y/o man with headaches, big hands, sweating, weakness, big feet, coarse facial features and skin tags
Acromegaly (unregulated GH secretion)
20 y/o with 3-day fever, chills, chest pain, cough w/ reddish brown sputum, rt. lower lobe consolodation with alpha hemolytic gram positive diplococci
Streptococcus pneumoniae (has a capsule, so immunity involves Abs to the capsule)
30 y/o female with weakness, headaches, depression, irritability, scleral icterus, small firm liver, tremor that resembles bird flapping its wings
Wilson's disease (inadequate copper excretion due to ATP7B mutation on chromosome 13). Copper spills into eye, liver and brain (parkinsonian sxs). Dx with high urinary copper, low ceruloplasmin level or slit lam eye exam (Kayser-fleischer rings in cornea)
35 y/o female with esophageal dysfunction and thickening skin.
Scleroderma (progressive autoimmune systemic sclerosis)
50 y/o female with weight loss, femoral neck fracture, lytic bone lesions, M protein spikes, Bence jones proteinuria, renal failure, anemia
Multiple myeloma
70 y/o female with muscle cramps, parathesias, carpopedal spasms when measuring blood pressure, involuntary facial twitch when ear is tapped.
Hypocalcemia (may be transient if, for example, a goiter is removed and parathyrois tissue is taken out with it)

Carpopedal spasms = Trosseau's sign
Involuntary facial twitch when facial nn is tapped = Chvostek's sign
30 y/o male smoker/drinker with gangrenous finger tips
Buerger disease (vasculitis causes segmental thrombosis in youg males with hx of early smoking)
30 y/o male smoker/drinker with gangrenous finger tips
Buerger disease (vasculitis causes segmental thrombosis in youg males with hx of early smoking)
Ovarian mass is a lymphoma with small lymphocytes, interspersed with macrophages and surrounded by clear spaces?
Classic "starry sky" appearance of Burkitt's Lymphoma (c-myc associated)
Man presents with decreased sperm motility, respiratory/earinfections
Kartagener Syndrome--dynein protein is defective, so cilia and flagella don't move correctly
15 y/o with headaches, paralyzed upwards gaze, bilateral papilledema, pupils that accomidate but don't react
Parinaud Syndrome: pineal tumor compresses pretectal area of dorsal midbrain (where vertical gaze center is) and also pinches the cerebral aquaduct
35 y/o female with 3rd degree burns and secondary infection gets hypoxia, hyaline membrane within alveolar walls, alveolar septal thickening, and neutrophilic infiltrate
ARDS!!! Key feature is hyaline membrane within alveolar walls
tingling in 1st, 2nd, 3rd digits on rt hand and loss of coordination/strength in rt thumb
Carpal tunnel affecting the median nn on right hand
25 y/o male with multiple small nodules on his lips, tall think build with long fingers, hyperextensible joints
MEN IIb has neuromas of mucosal surfaces and marfanoid habitus. Its assc with medullary carcinoma of the thyroid
Double vision reading or going down stairs gets better when head tilted to the right. Also strabismus with left eye elevated and extorted
Super oblique mm damaged (for example if CN V is damaged by trauma to the forehead)
5 y/o boy with yellow, soft, slightly raised bumps on his eyelids with no other sx's
Probably Familial hypercholesterolemia from a defect in LDL receptor gene. AutoDom, homozygotes get way worse disease
Young kid, good appetite but still underweight, bulky, greasy stools, persistent cough, wheezes, skin tastes salty
Cystic fibrosis (recessive epithelial Cl- channel defect), confirm dx with sweat test
Flushing, diarrhea, swelling of face/neck, wheezing, heart failure symptoms (esp. SOB)
Carcinoid syndrome from tumor secreting 5HT(look for excess 5-HIAA in the urine--a breakdown product of tryptophan/seratonin)
Problems digesting pizza, bread, cereal, pasta, etc....flatulence, weight loss and diarrhea result
Celiac disease (gluten intolerance due to IgA destruction of intestinal ECM..look for crypt cell hyperplasia, flattened villi, and lack of microvilli)
1.5 year old boy with recurrent infections, easy bruising, hepatosplenomegaly, and eczema
Wiskott-Aldrich Syndrome (X-link recessive defect in cytoskeletal protein, elevated IgA & IgE, low IgM & platelets...tx with bone marrow transplant from HLA-identical sibling or death by age 6)
17 /o boy with 1 year hx of multiple bacterial pneumonias, severe bronchiectasis, normal B&T cell counts, and "+" skin hypersensativity test to Candida
Common Variable Immunodeficiency (low level of all Igs, but normal Bcell level)
50 y/o transplant recipient ges headaches, nausea, vomitting and a CT shows "ring enhanced lesions" in his head (lungs clear, no rashes, no skin lesions)
Toxoplasmosis gondii (70% are seropositive and it became active when he was immunosuppressed...usually kept in check by cell-mediated immunity)
Frequent bacterial infections but no pus forms; 3 family members have it
Leukocyte Adhesion Deficiency (LAD); AutoRec, absence of CD18 (integrin), without integrin leukocytes can't migrate to inflammation sites
10 y/o from Haiti w/ SOB, wheezing, exertional dyspnea, urticaria, Ova/parasites in feces w/ nematode/eosinophilic infiltrates
Ascaris lumbricoides (possess potent allergens and migrates to lungs)
Kid, fever >10 days, dequamative rash on fingers/toes, cervical lymphadenopathy, bilateral conjunctavitis, polymorphous rash, oral lesions, pharyngeal erythema, strawberry tongue
Kawasaki Syndrome (mucocutaneous lymphnode syndrome)...assc with coronary artery aneurysms
16 y/o male with low levels of all Igs, normal B cell count, frequent bacterial infections
Common variable immuno deficiency
Turkish immigrant suffers from sensory loss/acid-fast granulomas on his extremities and cold areas (ie. ears)
Leprosy
nuclear homogenization (aka "ground glass nuclei"), Cowdry type A bodies, multinucleated cells
HIV encephalitis (patient will be immunocompromised...probably AIDS)
Young kid with chicken pox develops pernicious vomitting, lethargy, hepatomegaly, and coma 5 days later
Reyes Syndrome (post viral phenomenon, often assc with aspirin)
Child brain tumor with Rosenthal fibers that stains with GFAP
Pilocytic astrocytoma
34 y/o female with painful uirnation an knee pain, plus puss coming out of her eye)

aka: Urethritis, cervicitis, arthritis, and mucocutaneous lesions
Reiter's syndrome (assc with chlamydia)
72 y/o man with progressive memory loss, gait instability, and urinary incontinence (no tangles, plaques and a normal cerebral cortex)
intermittently raised pressure hydrocephalus (aka normal pressure hydrocephalus)...tx with ventricular shunt
65 y/o man has a colon polyp with saw-tooth glandular epithelium, goblet cell proliferation an columnar epithelieum
Hyperplastic polyp (90% of all colon polyps, benign)
1 year old gets fever/rash; 6 years later she's got seizures, behavior change, ataxia, focal neuralgias. She is soon quadraparetic and then dead.
Subacute Sclerosing Panencephalitis (SSPE); rare complication of measles (rubeola)
Patient from Bolivia has a blood film positive for Schuffner dots
Plasmodium vivax (P. ovale also has Schuffner dots--aka hypnozoites--but only vivax occurs in the western hemisphere)
Light shined in patient's right eye results in dilation of right eye and left eye
Marcus-Gunn Pupil seen in Multiple Sclerosis or right retinal detachment (right eye is getting so little light that it dilates to receive more and then sends the same dilation signal to the left eye)
25 y/o female with tremors, heat intolerance, weight loss, low TSH, no neck mass or opthalmopathy, and unilateral ovarian cystic mass
Monodermal teratoma (aka struma ovarii) making thyroid hormone

(note: mature teratomas cannot produce hormones)
17 y/o man with paroxysmal tachycardia, shortened PR interval, delta wave, and wide QRS complex on EKG
Wolff-Parkinson-White Syndrome (ventricular pre-excitation aasociated with an atrioventricular bypass track)