Diferencia entre revisiones de «Template:Hemolytic anemia DDX»
Sin resumen de edición |
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*[[Heparin-Induced Thrombocytopenia (HIT)]] | *[[Heparin-Induced Thrombocytopenia (HIT)]] | ||
*[[Hereditary spherocytosis]] | *[[Hereditary spherocytosis]] | ||
*[[Paroxysmal nocturnal hemoglobinuria]] | *[[Paroxysmal nocturnal hemoglobinuria]] (PNH) | ||
*[[ | *[[Malignant hypertension]] | ||
*[[Scleroderma]] | |||
*[[Antiphospholipid Syndrome (APS)]] | *[[Antiphospholipid Syndrome (APS)]] | ||
*Other medical causes: malignancy, renal allograft rejection, vasculitides like [[polyarteritis nodosa]] and [[Wegener's granulomatosis]] | *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 with mechanical, more common at aortic valve), [[LVAD]], [[TIPS]], coil embolization, patched AV shunt, [[AVM]] | *Nonvascular causes: prosthetic valve (more common with mechanical, more common at aortic valve), [[LVAD]], [[TIPS]], coil embolization, patched AV shunt, [[AVM]] | ||
Revisión actual - 19:21 12 may 2019
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 (PNH)
- Malignant hypertension
- Scleroderma
- Antiphospholipid Syndrome (APS)
- 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