Diferencia entre revisiones de «Template:Hemolytic anemia DDX»
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===Hemolytic | ===[[Microangiopathic Hemolytic Anemia (MAHA)]]=== | ||
*[[Disseminated Intravascular Coagulation (DIC)]] | *[[Disseminated Intravascular Coagulation (DIC)]] | ||
*[[Thrombotic Thrombocytopenic Purpura (TTP)]] | *[[Thrombotic Thrombocytopenic Purpura (TTP)]] | ||
*[[Hemolytic Uremic Syndrome (HUS)]] | *[[Hemolytic Uremic Syndrome (HUS)]] | ||
*[[HELLP syndrome]] | *[[HELLP syndrome]] | ||
*[[Heparin-Induced Thrombocytopenia (HIT)]] | *[[Heparin-Induced Thrombocytopenia (HIT)]] | ||
*[[Hereditary | *[[Hereditary spherocytosis]] | ||
*[[Paroxysmal nocturnal hemoglobinuria]] | *[[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]] | |||
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