Heme/Onc - bleeding/hypercoag - quiz Flashcards

1
Q

5 yr old boy - thrombocytopenia - abnormal GFR - recent diarrhea - schistocytes

A

HUS

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2
Q

HUS treatment

A

supportive; no antibiotics

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3
Q

48 yr old woman - thrombocytopenia - fever - delirium - schistocytes

A

TTP

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4
Q

TTP treatment

A

plasmaphoresis

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5
Q

33 yr old woman - stroke - hx 4 miscarriages

A

lupus anticoagulant

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6
Q

45 yr old woman - first DVT/no history - what do you want to check for?

A

malignancy

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7
Q

most common systemic vasculitis in children

A

Henoch-Schonlein purpura

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8
Q

4 yr old boy - palpable purpura over lower extremities - arthritis in knees and ankles

A

Henoch-Schonlein purpura

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9
Q

treatment for Henoch Schonlein purpura

A

prednisone

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10
Q

most common inherited bleeding disorder

A

von willebrand disease

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11
Q

initial treatment for ITP

A

corticosteroids

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12
Q

treatment for recurrent/relapsing ITP

A

splenectomy

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13
Q

your immediate handling of HIT

A
  1. discontinue heparin
  2. U/S LE for thrombosis
  3. give direct thrombin inhibitor
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14
Q

one key difference in labs for vit K deficiency and coagulopathy of liver disease

A

factor V: not impacted by vitamin K; decreased in CoLD

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15
Q

sudden thrombosis (3)

A
  1. polycythemia vera
  2. essential thrombocytosis
  3. HIT
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16
Q

essential thrombocytosis treatment

A

aspirin

hydroxyurea

17
Q

polycythemia vera lab value

A

extremely elevated Hct

18
Q

essential thromocytosis lab value

A

extremely elevated platelets

19
Q

polycythemia vera treatment

A

phlebotomy; NO iron supplementation

20
Q

polycythemia vera: erythropoietin high or low?

A

low (high RBCs not caused by high erythropoietin - in fact, high RBCs cause low erythropoietin)

21
Q

JAK2 associated with (3)

A
  1. polycythemia vera
  2. essential thrombocytosis
  3. myelofibrosis
22
Q

striking splenomegaly

A

myelofibrosis

23
Q

compare bone marrow of aplastic anemia, pure red cell aplasia, myelodysplasia

A

aplastic anemia: hypocellular
pure red cell aplasia: normocellular
myelodysplasia: hypercellular

24
Q

compare organ size of aplastic anemia, pure red cell aplasia, myelodysplasia

A

aplastic anemia: no organomegaly
pure red cell aplasia: no organomegaly
myelodysplasia: splenomegaly

25
Q

IgM binds RBC antigen in lower temps

A

cold agglutinin disease

26
Q

IgG binds RBC antigen at body temp

A

autoimmune hemolytic anemia

27
Q

onset around 6 mos old

A

beta thalassemia; sickle cell disease

28
Q

anemia definition

A

hct < 41 (male) <36 (female)

29
Q

basophilic stippling

A

beta thalassemia

30
Q

“bite” cells

A

G6PD disease

31
Q

3 platelet inhibitors

A

aspirin, clopidogrel, ticlopidine

32
Q

3 anticoagulants

A

warfarin, dabigatran, heparin/LMWH