Microangiopathic hemolytic anemia
From IDWiki
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
