Bleeding diathesis
Bleeding diathesis main page |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Mehrian Jafarizade, M.D [2]
Overview
Classification
Differential Diagnosis
Platelet disorders | Thrombocytopenia |
Infection-Induced Thrombocytopenia
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Drug-Induced Thrombocytopenia
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Heparin-Induced Thrombocytopenia
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Immune Thrombocytopenic Purpura (ITP)
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Inherited Thrombocytopenia
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Thrombotic Thrombocytopenic Purpura (TTP)
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Hemolytic Uremic Syndrome
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Thromobcytosis
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Thrombocytosis in response to acute or chronic inflammation has not been associated with an increased thrombotic risk. In fact, patients with markedly elevated platelet counts (>1.5 million), usually seen in the setting of a myeloproliferative disorder, have an increased risk of bleeding. This appears to be due, at least in part, to acquired von Willebrand disease (VWD) due to platelet-VWF adhesion and removal. | ||
Qualitative Disorders of Platelet Function
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Inherited Disorders of Platelet Function
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Acquired Disorders of Platelet Function
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von Willebrand Disease
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Vessel wall disorders | Metabolic and Inflammatory Disorders | ||
Inherited Disorders of the Vessel Wall | |||
Coagulation disorders | Fibrinogen | ||
Prothrombin | |||
Factor V | |||
Factor VII | |||
Factor VIII | |||
Factor IX | |||
Factor X | |||
Factor XI | |||
Factor XII | |||
HK | |||
Prekallikrein | |||
Factor XIII | |||
Hemophilia | Type A | ||
Type B | |||
Type C | |||
Rare diseases | Disseminated Intravascular Coagulation | ||
Vitamin K Deficiency | |||
Coagulation Disorders Associated with Liver Failure | |||
Acquired Inhibitors of Coagulation Factors |