2.2 Platelet and Vascular Disorders Flashcards
Thrombotic thrombocytopenic purpura (TTP) is characterized by:
Increased PLT aggregation
Thrombocytopenia may be associated with:
Hypersplenism
Aspirin prevents PLT aggregation by inhibiting the action of which enzyme?
Cyclo-oxygenase
Normal PLT adhesion depends on:
Glycoprotein Ib
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
PLT count
Bernard–Soulier syndrome is associated with:
Thrombocytopenia and giant PLTs
When performing PLT aggregation studies, which set of PLT aggregation results would most likely be associated with Bernard–Soulier syndrome?
Normal PLT aggregation to collagen, ADP, and epinephrine (EPI); decreased aggregation to ristocetin
Which set of PLT responses would be most likely associated with Glanzmann thrombasthenia?
Normal PLT aggregation to ristocetin; decreased aggregation to collagen, ADP, and EPI
Which of the following is a characteristic of acute immune thrombocytopenic purpura?
Spontaneous remission within a few weeks
TTP differs from DIC in that:
APTT is normal in TTP but prolonged in DIC
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?
Neonatal alloimmune thrombocytopenia
Which of the following is associated with post-transfusion purpura (PTP)?
Immune-mediated thrombocytopenia/alloantibodies
Hemolytic uremic syndrome (HUS) is associated with:
Escherichia coli 0157:H7
Storage pool deficiencies are defects of:
PLT granules
Lumi-aggregation measures:
PLT aggregation and adenosine triphosphate (ATP) release