HEME/ONC Flashcards

1
Q

What to look for someone w/ unprovoked thrombus?

  1. CANCER
  2. increased PTT, multiple SABs, false +VLDRL
  3. skin necrosis after warfarin is started
  4. MC inheritable pro-coag state. resistance to C
  5. heparin wont’ work. clots on heparin
  6. No Go for women >35 who smoke
  7. Pee out ATIII protein C +S preferentially. puts at risk for renal vein thrombosis
A
  1. CANCER
  2. increased PTT, multiple SABs, false +VLDRL- SLE
  3. skin necrosis after warfarin is started- Protein C/S def
  4. MC inheritable pro-coag state. resistance to C- Factor V leiden
  5. heparin wont’ work. clots on heparin- AT III deficiency
  6. No Go for women >35 who smoke- OCPs/HRT
  7. Pee out ATIII protein C +S preferentially. puts at risk for renal vein thrombosis- Nephrotic syndrome
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2
Q

7 days post-op, a patient deelops an arterial clot. her platelets are found to be 50% less than pre-op.

Mechanism?
Tx?

A

HIT!!!!

MOA- IgG to heparin bound to PF4
Tx- stop heparin, reverse warfarin w/ vit k and start lepirudin

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3
Q

patient walk in with thrombocytopenia and smear shows shistiocytes

  1. if PT and PTT are elevated, fibrinogen is decreased, D-Dimer and fibrin split products are elevated? causes? tx?
  2. If PT and PTT are normal? causes? tx?
A
  1. if PT and PTT are elevated, fibrinogen is decreased, D-Dimer and fibrin split products are elevated- DIC
    causes- sepsis, rhabdo, adenocarcinoma, heatstroke, pancreatitis, snake bites, OB stuff
    tx- FFP, platelet transfusion, correct underlying d/o
  2. If PT and PTT are normal- HUS or TTP
    causes- )157H7, ticlopidine, quinine, cyclosporine, HIV, Cancer
    tx- plasmapheresis… no platelets!!!!!
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4
Q

patient walk in with thrombocytopenia…30 yo F recurrent epistaxis, heavy menses and petechiae. decreased platelets only? tx?

A

ITP
tx w/ prednisone then splenectomy
IVIG if <10k rituximab

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5
Q

patient walk in with thrombocytopenia…. 20 yo f recurrent epistaxis, heavy menses, petechiae, normal plts, increased bleeding time and PTT. tx?

A

VWD

Tx- DDAVP for bleeding or pre-op. replace factor VIII (contains vWF) if bleeding continues

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6
Q

patient walk in with thrombocytopenia… 20 yp M recurrent bruising, hematuria, & hemarthroses, increased PTT that corrected w. mixing studies? tx?

A

Hemophilia

tx- if mild tx w/ DDAVP otherwise replace factors

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7
Q

patient walk in with thrombocytopenia…. 50 yo M meat-a-tarian just finished 2wks of clinda has hemarthroses and oozing at venipuncture sites? tx?

A

Vit. K def. decreased II, VII, IX, X. same for warfarin tox

Tx- w. FFP acutely + vitk shot

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8
Q

patient walk in with thrombocytopenia… 50 yo M beer-a-tarian w/ severe cirrhosis? 1st factor depleted? 2 factors not depleted?

A

Liver disease; GI bleeding is MC
1st factor depleted- VII, so PT increases first
2 factors not depleted- VII and vWF b/c they are made by endothelial cells

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9
Q

a patient walks in with microcytic anemia….

MCV=70
decreased Fe, retic., ferritin
increased TIBC, RDW

A

iron deficiency

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10
Q

a patient walks in with microcytic anemia….

MCV= 70
decreased Fe, TIBC, retic
nl ferritin

A

chronic anemia

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11
Q

a patient walks in with microcytic anemia….

MCV= 70
increased Fe, ferritin
decreased TUBC

A

sideroblastic anemia

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12
Q

a patient walks in with microcytic anemia….

MCV= 60
decreased RDW

A

thalassemia

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13
Q

a patient walks in with macrocytic anemia….

MCV= 100
decreased retic.
increased homocysteine
nl methylmelonic acid

A

FOLATE deficiency

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14
Q

a patient walks in with macrocytic anemia….

MCV= 100
acanthosytes

A

liver disease

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15
Q

a patient walks in with macrocytic anemia….

MCV= 100
decreased retic
increased homocysteine, methylmelonic acid

A

B12 deficiency

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16
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

A

hemolysis

17
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

  1. sickle cell kid w/ sudden drop in Hct
A

aplastic crisis

sickle crisis from hypoxia, dehydration or acidosis

18
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

  1. cyanosis of fingers, ears, nose + recent mycoplasma infx
A

cold agglutinins; destruction occurs in the liver; IgM mediated

19
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

  1. sudden onset after PCN, ceph, sulfas, rifampin or Ca tx?
A

warm agglutinins; destruction in spleen

tx w/ steroids then splenectomy

20
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

  1. splenomegaly, +FH, biliruibin, gallstones, Increased MCHC. tx?
A

hereditary spherocytosis (loss of spectrin)

tx w/ splenectomy

21
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

  1. Dark urine in AM, Budd-Chiari syndrome
A

Paroxysmal nocturnal hemoglobinuria. defect PIG-A lysis by complement.
*increased risk for aplastic anemia

22
Q

Normal MCV, increased LDH + indirect bilirubin, decreased haptoglobin

  1. sudden onset after primiquine, sulfa and fava beans
A

G6PDH def. Heinz bodies, bite cells

avoid oxidant stress