UW Pre-Reset Flashcards
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FATRN: fever, anemia (microangiopathic hemolytic anemia), thrombocytopenia, renal insufficiency, neuro *HA confusion, dx? mgmt?
TTP! (small vessel thrombi that consume platelets, shear RBCs, and cause end organ damage; emergency tx w/ plasma exchange +/- steroids. TTP is caused by def in plasma protease ADAMTS13 (d/t formation of autoantibody); lots of vWF accumulate on endothelial wall trapping platelets and generate thrombi
TTP vs HUS
Very similar in that both cause MAHA and thrombocytopenia; except HUS a/w E. coli and is primarily a disorder of renal system - no neuro findings or fever
MAHA - microangiopathic hemolytic anemia on peripheral blood smear?
Schistocytes/RBC fragments
Pt w/ recent fever, chills, productive cough, and leukocytosis has 3rd episode of RLL pneumonia in past several months
Recurrent pneumonia occurring in the same anatomic location of lung raises suspicion for localized airway obstruction, which if present can lead to impaired bacterial clearance and predisposition to infection; get CT to r/o cancer
PFTs for chronic lung diseases: asthma, COPD, ILD/restrictive chest wall disease
Asthma and COPD: normal to inc TLC, dec FEV1/FVC, DLCO dec in COPD but normal in asthma
ILD/restrictive chest wall (restrictive pattern): dec TLC, normal FEV1/FVC, dec DLCO for ILD and normal for restrctive chest wall disease
Splenic abscess p/w fever, leukocytosis, LUQ pain; pts develop left sided pleuritic chest pain and left pleural effusion and splenomegaly, risk factors for splenic abscess?
Hematogenous spread ie infective endocarditis
Pure motor hemiparesis, lesion where?
Lacunar stroke (single modality defect) affecting posterior limb of internal capsule (commonly a/w chronic HTN which leads to arteriolar sclerosis)
47yo man, recurrent blisters on dorsum of his hand and forearm, fatigue and occasional joint pain, elevated transaminases, dx?
Porphyria cutanea tarda d/t chronic hepatitis C virus (other extra hepatic manifestations = mixed cyroglobuinemia syndrome *paplpable purpura, athralgias, glomerulonephritis, low
complement), lichen planus
Lady w/ transient (lasting just hours) of foot drop and sensory changes over dorsal foot and lateral shin; PE shows impaired ankle dorsiflexion and great toe extension w/ preserved plantar flexion and reflexes, dx?
Common fibular neuropathy aka common peroneal d/t peripheral nerve compression; common peroneal travels near fibular head and is susceptible to compressive injuries eg cast/bedrest/leg crossing. This is not MS since resolved in hours (MS episodes take days to weeks)
Edema in just the UE, venous congestion in anterior chest, dx?
Superior vena cava syndrome (60% of cases d/t cancer, get cxr)
Muffled voice, deviated uvula w/ unilateral lymphadenopathy, dx and mgmt?
Tonsilitis -> progressed to peritonsilar abscess; dx w/ needle peritonsilar aspiration and give IV abx
Dvlpt of clubbing and sudden onset joint arthropathy in a chronic smoker, dx?
Hypertrophic osteoarthropathy, this condition is a/w lung cancer, get cxr
vWF blood panel findings? DIC findings?
vWF deficiency = prolonged bleeding and aPPT, normal platelets
DIC = consumption of all coagulation cascade components - thrombocytopenia, microangiopathic hemolytic anemia, low clotting factors (fibrinogen, factors V and VIII), and prolonged PT and aPTT
Lady w/ fluctuating double vision, found to have antibodies against nicotinic receptors on the motor end plate, next steps?
She has myasthenia; get CT scan chest to look for thymoma that is operable since that can lead to long-term improvement; side note while ACH receptor antibodies are highly specific - other tests for MG include muscle specific tyrosine kinase antibodies -> EMG -> or edrophonium test (less specific though since it is just acetylcholinesterase inhibitor)
Complication of dermatomyositis that over 15% of adult pts will develop or have?
Malignancy commonly ovarian, lung, pancreatic, stomach, colorectal, non-Hodgkin
Anti-RNP, anti-Jo-1, dx?
Dermatomyositis
Persistence of nocturnal and early morning penile erections helps ddx psychogenic from organic causes of male ED
Normal nocturnal erections indicate vascular and nerve function
Old lady, focal neuro symptoms - drops spoon, right sided weakness - followed by vomiting, pressures of 180/105, dx?
Intracranial hemorrhage 2/2 HTN occurring commonly in basal ganglia, thalamus, pons, cerebellum. Pts present w/ focal symptoms progressing to signs of elevated ICP (nausea, vomiting, HA)
Other bugs involved w/ GBS besides campy
Herpes viruses, mycoplasma, haemophilus influenzae; GBS occurs more frequently in pts w/ lymphoma, sarocoidosis, SLE
Hemolysis can occur intra or extra vascularly
Intravascular hemolysis is d/t significant RBC structural damage resulting in RBC destruction within intravascular space (eg paroxysmal nocturnal hemoglobinuria, or DIC) Extravascular hemolysis: RBCs predominantly destroyed by phagocytes in the reticuloendothelial system (eg lymph nodes, spleen). Less HgB release than intravascular hemolysis but still low haptoglobin, elevated LDH and elevated indirect bilirubin. Extravascular is d/t antibody mediated RBC destruction (AIHA), intrinsic RBC enzyme (G6PD def) or membrane defects (hereditary spherocytosis) *AIHA vs hereditary spherocytosis: same spherocytes, but AIHA is coombs positive while hereditary is family hx auto dom/negative Coombs/positive osmotic fragility test
Dramatic leukocytosis, absolute basophilia, shift towards very early neutrophil precursor cells (promyelocytes, myelocytes), dx? Use what score to ddx from leukemoid rxn?
Chronic myeloid leukemia. Leukocyte alkaline phosphatase score is low in CML while it is high in leukemoid reaction (which is caused by severe infection where as CML is d/t BCR-ABL fusion). More myelocytes in CML, more metamyelocytes in leukemoid rxn
Blood transfusion following liver injurt from MVA, now w/ numbness in fingertips/lips, forceful flexion of wrist w/ abduction of the thumb while nurse measures BP (trousseau signs), dx?
Acute hypocalcemia (chelation - blood citrate from transfusion binds free ionized calcium causing functional hypocalcemia)
RA vs Parvovirus B19 infection
RA presents w/ joint stiffness for at least an hr in the morning, joint swelling, and symptoms for > 6 weeks
B19: although similar joints affected as RA (MCP, PIP, wrist) symptoms are acute (10 days) and there was absence of joint swelling or prolonged joint stiffness in the morning; look for erythema infectiosum rash/diarrhea/fatigue/fever; look for anti-B19 IgM antibodies but self-resolving course
Bugs that can cause infective endocarditis?
Staph aureus, viridans, staph epidermidis, enterococci (nosocomial UTI question), strep bovis, fungi