Thrombotic microangiopathy: Difference between revisions
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*Associated with coexisting condition |
*Associated with coexisting condition |
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**Autoimmune disease, including [[systemic lupus erythematosus]] or [[antiphospholid antibody syndrome]] |
**Autoimmune disease, including [[systemic lupus erythematosus]] or [[antiphospholid antibody syndrome]] |
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| − | ** |
+ | **[[Drug-induced thrombotic microangiopathy]], including [[quinine]], [[ticlopidine]], and [[chemotherapy]] ([[mitomycin]], [[gemcitabine]], [[cyclosporine]], and [[tacrolimus]], though it may also be caused by the underlying condition) |
| + | **[[Sepsis]] and [[secondary hemolytic-uremic syndrome]] (usually from [[Streptococcus pneumoniae]] or [[influenza]]) |
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| − | **[[Sepsis]] |
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**[[DIC]] |
**[[DIC]] |
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**[[Malignancy]] |
**[[Malignancy]] |
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Revision as of 09:51, 20 April 2023
- Syndrome of microangiopathic hemolytic anemia, thrombocytopenia, and microvascular thrombosis leading to organ dysfunction
- Primary
- Associated with coexisting condition
- Autoimmune disease, including systemic lupus erythematosus or antiphospholid antibody syndrome
- Drug-induced thrombotic microangiopathy, including quinine, ticlopidine, and chemotherapy (mitomycin, gemcitabine, cyclosporine, and tacrolimus, though it may also be caused by the underlying condition)
- Sepsis and secondary hemolytic-uremic syndrome (usually from Streptococcus pneumoniae or influenza)
- DIC
- Malignancy
- HIV
