2.2 Platelet and Vascular Disorders Flashcards

1
Q

Thrombotic thrombocytopenic purpura (TTP) is characterized by:

A

Increased PLT aggregation

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2
Q

Thrombocytopenia may be associated with:

A

Hypersplenism

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3
Q

Aspirin prevents PLT aggregation by inhibiting the action of which enzyme?

A

Cyclo-oxygenase

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4
Q

Normal PLT adhesion depends on:

A

Glycoprotein Ib

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5
Q

Which of the following test results is normal in a patient with classic von Willebrand disease?

A. PLT aggregation
B. APTT
C. PLT count
D. Factor VIII:C and von Willebrand factor (VWF) levels

A

PLT count

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6
Q

Bernard–Soulier syndrome is associated with:

A

Thrombocytopenia and giant PLTs

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7
Q

When performing PLT aggregation studies, which set of PLT aggregation results would most likely be associated with Bernard–Soulier syndrome?

A

Normal PLT aggregation to collagen, ADP, and epinephrine (EPI); decreased aggregation to ristocetin

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8
Q

Which set of PLT responses would be most likely associated with Glanzmann thrombasthenia?

A

Normal PLT aggregation to ristocetin; decreased aggregation to collagen, ADP, and EPI

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9
Q

Which of the following is a characteristic of acute immune thrombocytopenic purpura?

A

Spontaneous remission within a few weeks

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10
Q

TTP differs from DIC in that:

A

APTT is normal in TTP but prolonged in DIC

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11
Q

Several hours after birth, a baby boy develops petechiae and purpura and hemorrhagic diathesis. The PLT count is 18 × 109/L. What is the most likely explanation for the low PLT count?

A

Neonatal alloimmune thrombocytopenia

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12
Q

Which of the following is associated with post-transfusion purpura (PTP)?

A

Immune-mediated thrombocytopenia/alloantibodies

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13
Q

Hemolytic uremic syndrome (HUS) is associated with:

A

Escherichia coli 0157:H7

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14
Q

Storage pool deficiencies are defects of:

A

PLT granules

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15
Q

Lumi-aggregation measures:

A

PLT aggregation and adenosine triphosphate (ATP) release

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16
Q

Neurological findings may be commonly associated with which of the following disorders?

A

TTP

17
Q

Which of the following is correct regarding acquired TTP?

A

Autoimmune disease

18
Q

Hereditary hemorrhagic telangiectasia is a disorder of:

A

Connective tissue

19
Q

Which of the following prevents PLT aggregation?

A. TXA2
B. Thromboxane B2
C. Prostacyclin
D. Antithrombin (AT)

A

Prostacyclin

20
Q

Which defect characterizes Gray syndrome?

A

Alpha granule defect

21
Q

The P2Y12 ADP receptor agonist assay may be used to monitor PLT aggregation inhibition to which of the following drugs?

A

Clopidogrel (Plavix)

22
Q

Which of the following instruments can be used to evaluate PLT function?

A. PLT aggregometer
B. VerifyNow
C. PFA-100
D. All of the above

A

All of the above

23
Q

Which of the following PLT aggregating agents demonstrates a monophasic aggregation curve when used in the optimal concentration?

A

Collagen