Asdfg Flashcards

(22 cards)

1
Q

o Dohle-like bodies are present in neutrophils
o FUNCTION: NORMAL

A

MAY-HEGGLIN ANOMALY

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2
Q

MAY-HEGGLIN ANOMALY

MUTATION:

A

MYH9 gene = abnormal size platelets

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3
Q
  • reflecting bone marrow failure
  • affected infants = ≤ 20,000/uL at birth
  • petechiae and evidence of bleeding and frequent anomalies
A

CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA

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4
Q

CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA

  • MUTATION: _____ gene on _____ chromosome
  • Complete loss of THROMBOPOIETIN RECEPTOR function
  • reduced megakaryocyte progenitors and high thrombopoietin levels
A

MPL gene on Chromosome 1 (1p34.1)

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5
Q

(Ans)FALSE:
AUTOSOMAL DOMINANT THROMBOCYTOPENIA

• MUTATION:______ gene on the short arm of chromosome______

A

ANKRD26

10(10p12.1)

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6
Q

(Ans)FALSE:
AUTOSOMAL DOMINANT THROMBOCYTOPENIA

• MUTATION:______ gene on the short arm of chromosome______

A

ANKRD26

10(10p12.1)

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7
Q
  • most common infectious agent
  • 0.5-1% of all birth
A

CYTOMEGALOVIRUS: (Ans)

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8
Q

lead to incomplete megakaryocyte differentiation and
resultant thrombocytopenia

A

(Ans)FALSE:
AUTOSOMAL DOMINANT THROMBOCYTOPENIA

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9
Q
  • More common than THROMBOTIC THROMBOCYTOPENIC PURPURA
A

HEMOLYTIC UREMIC SYNDROME(Ans)

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10
Q
  • Caused by Shigella dysenteriae serotype or enterohemorrhagic E.coli OH serotypes (0157:H7)
A

HUS

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11
Q
  • HALLMARK SIGNS: Mild thrombocytopenia, mild anemia, bloody diarrhea and AKI
A

HUS

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12
Q
  • Common cause of destructive thrombocytopenia
A

DISSEMINATED INTRAVASUCLAR COAGULATION(ans)

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13
Q
  • Common cause of destructive thrombocytopenia
A

DISSEMINATED INTRAVASUCLAR COAGULATION(ans)

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13
Q
  • Function: Normal
  • Morphology: Normal
  • Aggregation test: Normal
A

REACTIVE Thrombocytosis(Ans)

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14
Q
  • normalize the count
  • Thrombosis with IDA
A

TREATMENT of IDA(ans)

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15
Q
  • Chronic myeloproliferative neoplasm, is the most common cause of thrombocytosis
A

ESSENTIAL THROMBOCYTHEMIA (ans)

16
Q

ACUTE PHASE REACTANTS (Ans)
- APR in Thrombosis associated with inflammation

A
  • Fibrinogen, VWF
17
Q

Moschcowitz Syndrome(ans)

▪ TRIAD OF:

A

MAHA, Thrombocytopenia & Neurologic abnormalities

18
Q
  • Peaks 10-17 days after withdrawal of the offending drug or after
    institution of therapy for the underlying condition
A

REBOUND THROMBOCYTOSIS(ans)

19
Q

Moschcowitz Syndrome(ans)

▪ TRIAD OF:

A

MAHA, Thrombocytopenia & Neurologic abnormalities

19
Q

▪ TRIAD OF: MAHA, Thrombocytopenia & Neurologic abnormalities

A

Moschcowitz Syndrome(ans)

20
Q

REBOUND THROMBOCYTOSIS(ans)
- Peaks ______after withdrawal of the offending drug or after
institution of therapy for the underlying condition