Template:Hemolytic anemia DDX: Difference between revisions
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*[[Hereditary spherocytosis]] | *[[Hereditary spherocytosis]] | ||
*[[Paroxysmal nocturnal hemoglobinuria]] | *[[Paroxysmal nocturnal hemoglobinuria]] | ||
*Other medical causes: [[malignant hypertension]], [[HELLP]], [[Antiphospholipid Syndrome (APS)]], [[scleroderma]], [[Paroxysmal Nocturnal Hemoglobinuria (PNH)]], malignancy, renal allograft rejection, vasculitides like [[polyarteritis nodosa]] and [[Wegener's granulomatosis]] | |||
*Drugs: chemotherapy; [[Clopidogrel]] (Plavix) associated with [[TTP]] | |||
*Nonvascular causes: prosthetic valve (more common w/ mechanical, more common at aortic valve), [[LVAD]], [[TIPS]], coil embolization, patched AV shunt, [[AVM]] | |||
Revision as of 13:08, 29 June 2015
Microangiopathic Hemolytic Anemia (MAHA)
- Disseminated Intravascular Coagulation (DIC)
- Thrombotic Thrombocytopenic Purpura (TTP)
- Hemolytic Uremic Syndrome (HUS)
- HELLP syndrome
- Heparin-Induced Thrombocytopenia (HIT)
- Hereditary spherocytosis
- Paroxysmal nocturnal hemoglobinuria
- Other medical causes: malignant hypertension, HELLP, Antiphospholipid Syndrome (APS), scleroderma, Paroxysmal Nocturnal Hemoglobinuria (PNH), malignancy, renal allograft rejection, vasculitides like polyarteritis nodosa and Wegener's granulomatosis
- Drugs: chemotherapy; Clopidogrel (Plavix) associated with TTP
- Nonvascular causes: prosthetic valve (more common w/ mechanical, more common at aortic valve), LVAD, TIPS, coil embolization, patched AV shunt, AVM
