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26 Cards in this Set
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- Back
- 3rd side (hint)
Impaired / Decreased platelet count |
BERNARD-SOULIER syndrome Fanconi anemia TAR syndrome Viral infection Leukemia Megaloblastic anemia WISKOTT-ALDRICH syndrome MAY-HEGGLIN ANOMALY |
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increased platelet destruction |
HUS DIC ITP TTP HIT |
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Increased splenic sequestration |
gaucher disease hodgkin disease sarcoidosis lymphoma cirrhosis of liver portal hypertension |
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Reactive lymphocytosis other name |
secondary thrombocytosis |
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Autonomous thrombocytosis other name |
primary thrombocytosis |
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autonomous thrombocytosis example of associated diseases |
Essential thrombocythemia Chronic myelogenous leukemia Polycythemia vera Primary myelofibrosis |
EC PP (easy pp) |
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Platelet adhesion disoders |
Bernard soulier syndrome von Willebrand disease |
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Platelet aggregation disoder |
Glanzmann's thrombasthenia |
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Platelet secretion disorder |
Thromboxane pathway disorder |
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deficiency of GP 1b/IX/V |
Bernard soulier syndrome |
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Platelet receptor for vWF |
GP 1b/IX/V |
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Normal aggregation with
ADP Collagen Epinephrine |
Bernard soulier syndrome vWD |
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Abnormal aggregation with restocetin |
Bernard soulier syndrome |
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most common vWD, mild bleeding tendencies |
type 1 |
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most severe in bleeding tendencies type of vWD, rarest type |
type 3 |
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Platelet fibrinogen receptor |
GP IIb/IIIa |
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Abnormal aggregation response in ACE |
glazmann thrombasthenia |
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normal aggregation in restocetin |
Glazmann thrombasthenia |
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Alpha granules deficiency |
gray platelet syndrome |
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dense granule deficiencies |
hemansky-pudak chediak-higashi syndrome TAR syndrome Wiskott-aldrich syndrome |
basta gwapo dense na sila |
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X-linked recessive inheritance |
wiskott-aldrich syndrome |
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gradual increase from low platelet until normal in adult (1 year old) |
TAR syndrome |
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Oculocutaneous albinism |
Hermansky-pudlak syndrome |
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Partial albinism |
Chediak-higashi syndrome |
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deficiency of GP IIb/IIIa autosomal recessive |
Glanzmann's thrombobasthenia |
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Increase BT Abnormal clot retraction |
Glanzmann thrombasthenia |
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