Template:Hemolytic anemia DDX: Difference between revisions
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*[[Hereditary spherocytosis]] | *[[Hereditary spherocytosis]] | ||
*[[Paroxysmal nocturnal hemoglobinuria]] | *[[Paroxysmal nocturnal hemoglobinuria]] | ||
*[[malignant hypertension]] | |||
*[[Antiphospholipid Syndrome (APS)]] | |||
* | *[[scleroderma]] | ||
*Other medical causes: malignancy, renal allograft rejection, vasculitides like [[polyarteritis nodosa]] and [[Wegener's granulomatosis]] | |||
*Drugs: chemotherapy; [[Clopidogrel]] (Plavix) associated with [[TTP]] | *Drugs: chemotherapy; [[Clopidogrel]] (Plavix) associated with [[TTP]] | ||
*Nonvascular causes: prosthetic valve (more common | *Nonvascular causes: prosthetic valve (more common with mechanical, more common at aortic valve), [[LVAD]], [[TIPS]], coil embolization, patched AV shunt, [[AVM]]) | ||
Revision as of 13:09, 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
- malignant hypertension
- Antiphospholipid Syndrome (APS)
- scleroderma
- Other medical causes: 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 with mechanical, more common at aortic valve), LVAD, TIPS, coil embolization, patched AV shunt, AVM)
