3 Flashcards

(33 cards)

1
Q

features of sicca syndrome and best initial and diagnostic test

A
  • dry eyes, dry mouth

- secretory deficiency (Schrimer test) and autoantibody screen

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2
Q

positive biferengence test with rhomboid crystals is what? what disease is it related to?

A

pseudogout, seen in hemochromatosis

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3
Q

features of sarcoidosis

A
  • erythema nodosum
  • peripheral nerve disease
  • hepatic compromise
  • hilar lymph node enlargement–> need x-ray to diagnose
  • young population
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4
Q

definite diagnosis of sarcoidosis

A

biopsy of:

  • any palpable lymph node
  • subq nodule except erythema nodosum
  • enlarged parotid
  • lacrimal gland
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5
Q

Drugs that affect lithium level

A
  • diuretics
  • NSAIDs except aspirin
  • SSRI
  • Ace-I and ARBs
  • antiepileptics
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6
Q

Management of lobular carcinoma in situ (nonmalignant– DCIS is worse)

A
  • excisional biopsy then follow up surveillance

- alternative option: tamoxifen or raloxifene

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7
Q

Features and tests for chronic pancreatitis

A
  • steatorrhea secondary to fat malabsorption (bulky foul smelling stool difficult to flush)
  • epigastric pain with radiation to the back
  • text: CT scan of abdomen, NOT serum lipase and amylase (more for acute pancreatitis)
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8
Q

Treatment of chronic pancreatitis

A
  • first line: alcohol cessation and small meals with low fat
  • pancreatic enzymes and possible opiate medications
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9
Q

Endometriosis treatment

A
  • meds– NSAIDs, GnRH analogs, danazol (synthetic androgen), oral contraceptives
  • surgery
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10
Q

Medications in recent MI (q waves in lead II, III, avF)

A
  • antiplatelets
  • beta blocker
  • statins
  • Ace-I or ARB
  • aldosterone antagonist (eplerenone) IF LVEF <40%, add to beta blocker and ace-i
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11
Q

when should EGD be considered instead of colonoscopy as first step in hematochezia?

A
  • UGIB suspected

- hemodynamically unstable

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12
Q

How does biliary colic present?

A

constant epigastric or RUQ pain, can radiate to shoulder

  • n/v/diaphoresis
  • <6 hours
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13
Q

Management of gallstones w/ vs w/o stones on imaging

A

with: cholecystectomy, or ursodeoxycholic acid in poor surgical candidates or patients refusing surgery
without: CCK- stimulated cholesyntigraphy

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14
Q

How does amaurosis fugax present?

A
  • transient monocular blindness

- carotid bruit

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15
Q

How does IgA nephropathy usually present?

A
  • gross hematuria following acute URI
  • flank pain
  • dysmorphic RBCs in urine
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16
Q

How does acute post strep glomerulonephritis usually present?

A
  • strep throat/skin infection, then 10 days later renal issues
  • hypertensive
  • urine cast shows RBCs and RBC casts
  • decreased complement levels
17
Q

Timing, pathophysiology and signs of breastmilk jaundice

A
  • starts at 3-5 days, peaks at 2 weeks
  • high beta-glucuronidase in breast milk deconjugates intestinal bili and increase enterohepatic circulation
  • normal exam, spontaneous resolution
18
Q

Best prognostic indicator of acute pancreatitis

19
Q

Positive LR vs Negative LR

A
\+= sensitivity/ 1- specificity
-= 1- sensitivity/specificity
20
Q

Which antibodies correlate to disease activity in SLE?

A

anti-ds DNA (most sensitive marker for disease as well)

21
Q

Treatment of SLE

A

hydroxychloroquine and prednisone

22
Q

Initial management of adrenal masses?

A
  • studies of hormonal production: dexamethasone suppression, 24 hr urine catecholamines, metanephrine, VMA, etc
  • if >4cm, then surgical excision
23
Q

Treatment of sunburn from doxy

A

NSAIDs, steroids if severe

24
Q

SE of isotretinoin (acne med)

A

hyperglycemia, hyptertriglyceridemia, hepatotoxicity, mucocutaneous rxns, teratogen (females need 2 concurrent contraception methods)

25
Treatment of hypertrophic cardiomyopathy
- first line: beta blockers | - verapamil, disopyramide
26
how does traumatic LP present?
- high RBCs without xanthochromia (this presents with SAH) - high protein, high glucose - WBC 1 in 1000 when compared to RBCs
27
Risk factors for CRC
- family history, FAP - IBS - Af American - alcohol intake, smoking >30 years - obesity
28
What does paroxysmal supraventricular tachycardia look like on EKG?
- Abrupt onset - unidentifiable P waves - narrow and regular QRS complexes
29
4 Ts of HIT
- thrombocytopenia - timing of drop (onset 5-10 days or <1 day if prior exposure in last 30 days for 2 points) - thrombosis - other causes
30
Treatment of HIT
discontinue all forms of heparin, including warfarin start direct thrombin inhibitor (i.e. argatroban) avoid all forms of heparin for life
31
What is endophthalmitis? tx?
- infection of vitreous fluid - swollen eyelids, hypopon (layer of leukocytes in anterior chamber), conjunctivitis - tx: aspiration and vitrectomy, antibiotics via intravitreal route
32
What should you watch for in patients with autosomal dominant polycystic kidney disease? Most common extrarenal manifestation?
- renal function decline-- treat with ACE-i - hypertension (maintain <130/80), NOT extrarenal manifestation - most common extra renal: hepatic cysts - 10% have berry aneurysms, only needs to be screened for family with positive SAH hx.
33
choice of screening for asymptomatic family members with ADPKD
ultrasound