Medicine 3 Flashcards
Management of Asx Lymphadenopathy?
If ≤1.0 cm + No Symptoms = OBSERVE (even if multiple and painless)
Hemochromatosis patients @increase risk for infection with (3)?
Listeria
Vibrio Vulnificus
Yersinia
Patient with persistent respiratory complaints and known viral URI comes with purulent cough, hemoptysis. CXR with many small thin cavities. Dx?
Acute Necrotizing PNA with Pneumatoceles (Staph Aureus complication of viral URI)
Endophthalmitis
- MCC
- Definition
- Key PE Finding in Eye
- W/U (2)
- Tx (2)
- MCC: s/p cataract surgery
- Definition: infection within the eye (vitreous)
- Key PE Finding in Eye: Hypopyon (~severe uveitis)
- W/U (2): Cx + Gram Stain of Vitreous
- Tx (2): intra-vitreous Abx —> vitrectomy
4 Anterior Mediastinal Masses
4 Anterior Mediastinal Masses
- Teratoma (and other Germ Cells), Terrible Lymphoma, Thymoma, Thyroid
5 Germ Cell Tumors
Seminoma (xAFP, aka dysgerminoma in women), Chorio (hCG), Endodermal Yolk (AFP), Teratoma, Embryonal
2 Stromal Tumors
Leydig + Sertoli / Granulosa + Theca
3 Transplant Rejection
- Timing
- Paph
- Tx
- Hyperacute
- Timing: minutes
- Paph: pre-formed antibodies –> vascular occlusion –> ischemic/necrosis - Acute
- Timing: weeks-months
- Paph: Host CTL against graft –> perivascular lymphocytic vasculitis
- Tx: Immunosuppresion/steroids - Chronic
- Timing: months-years
- Paph: non-self MHC are viewed by host CTLs as self MHCs presenting foreign peptides —> Fibrosis
- Tx: none, irreversible
Charcot Joint
- MCC (2)
- Paph
- XRay Findings (3)
- Management
- MCC (2) = DM + B12
- Paph: xProtopathic/epicritic –> increase trauma
- XRay Findings (3): effusion, osteophytes, loose fragments
- Management: underlying conditions + low weight-bearing device
Heat Stroke
- Criteria (4)
- Paph
- Tx
Criteria
- Temp >104 (40)
- Collapse
- CNS Dysfunction
- End Organ Damage (ARF, Rhabdo, Nose Bleeds)
Paph: elevated central temperature = inability of hypothalamus to regulate body cooling
Tx = rapid cooling with ice water immersion
(T/F) In Sheehan’s postpatum necrosis:
- Aldosterone level is low
- Na is low, K is high
FALSE; recall the zona glomerulosa is ACTH independent (AngII dependent).
Bottom Line: primary adrenal failure = xAldosterone, but secondary adrenal failure = normal Aldosterone
Paph of Malignant Hyperthermia
Autosomal dominant inheritance of abnormal Ca cells in myocytes; increase risk with halothane/succinylcholine
Patient with primary hyperAldo is given spironolactone for control of aldosterone. Develops gynecomastia. Next step?
Switch to eplerenone (selective mineralocorticoid antagonist)
Tx of Warm (3) vs. Cold (1) AIHA
Warm: steroids –> rituximab –> splenectomy
Cold: warm them!
Describe Heinz bodies. When should you measure G6PD enzyme activity level in a symptomatic patient?
Heinz Bodies = ferrous –> ferric state
G6PD levels in ACUTE attack are NORMAL b/c all the abnormal RBC are hemolyzed; measure 120 days later
MCC risk factor for aortic dissection?
Systemic HTN
Rx approved for treatment + prophylaxis of secondary amyloidosis?
Colchicine
Acromegaly
- Screening Test
- Diagnostic Test
Screening: IGF1 b/c if low rules out acromegaly
Diagnostic: Glucose load GH suppression test (just like how saline load suppression for hyperAldo and dexamethasone suppression for Cushings)
Triad for Disseminated GC infection?
Think PST
- Polarthritis
- Skin Rash (PAINLESS vesicopustular lesions)
- Tenosynovitis
____ worsens wafarin vs. _____ inhibits warfarin.
___ Increase risk for warfarin induced skin necrosis
Acetaminophen worsens Warfarin (increase bleeding)
Spinach (VitK = replenish clotting factors) antagonizes Warfarin
Protein C deficiency increases risk for necrosis