Microangiopathic hemolytic anemia: Difference between revisions
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==Differential Diagnosis== |
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*Primary/[[Thrombotic microangiopathy|thrombotic microangiopathies]] (TMA) |
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**[[Thrombotic thrombocytopenic purpura]] (TTP) |
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***Congenital ([[Upshaw-Shulman syndrome|Upshaw-Shulman]]) |
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***Acquired |
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**[[Hemolytic uremic syndrome]] (HUS) |
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***Typical (Shiga-producing [[Escherichia coli]]) |
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***[[Atypical hemolytic uremic syndrome]] (aHUS) (congenital complement-overactivation) |
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*Secondary |
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**[[Antiphospholid antibody syndrome]] |
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**[[Malignant hypertension]] |
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**[[Lymphoma|Lymphomas]] and solid tumours |
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**[[Scleroderma]] crisis |
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**Drug-associated: [[Calcineurin inhibitor|calcineurin inhibitors]], [[quinine]], [[ticlopidine]] |
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**[[Vasculitis]] |
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**Infections: [[HIV]], [[influenza]], [[EBV]], [[parvovirus]] |
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**[[Disseminated intravascular coagulation]] (DIC) |
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**[[HELLP syndrome]] |
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[[Category:Hematology]] |
[[Category:Hematology]] |
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Revision as of 13:04, 2 August 2020
Differential Diagnosis
- Primary/thrombotic microangiopathies (TMA)
- Thrombotic thrombocytopenic purpura (TTP)
- Congenital (Upshaw-Shulman)
- Acquired
- Hemolytic uremic syndrome (HUS)
- Typical (Shiga-producing Escherichia coli)
- Atypical hemolytic uremic syndrome (aHUS) (congenital complement-overactivation)
- Thrombotic thrombocytopenic purpura (TTP)
- Secondary
- Antiphospholid antibody syndrome
- Malignant hypertension
- Lymphomas and solid tumours
- Scleroderma crisis
- Drug-associated: calcineurin inhibitors, quinine, ticlopidine
- Vasculitis
- Infections: HIV, influenza, EBV, parvovirus
- Disseminated intravascular coagulation (DIC)
- HELLP syndrome
