Thrombotic microangiopathy: Difference between revisions
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|[[Hemolytic-uremic syndrome]] |
|[[Hemolytic-uremic syndrome]] |
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|PT/INR and PTT are normal |
|PT/INR and PTT are normal, severe AKI |
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|[[Atypical hemolytic-uremic syndrome]] |
|[[Atypical hemolytic-uremic syndrome]] |
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|PT/INR and PTT are normal |
|PT/INR and PTT are normal, severe AKI |
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|[[HELLP syndrome]] |
|[[HELLP syndrome]] |
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|pregnancy |
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! colspan="2" |Secondary |
! colspan="2" |Secondary |
Latest revision as of 11:26, 19 March 2024
- Syndrome of microangiopathic hemolytic anemia, thrombocytopenia, and microvascular thrombosis leading to organ dysfunction
Disease | Clinical Clues |
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Primary | |
Thrombotic thrombocytopenia purpura | PT/INR and PTT are normal |
Hemolytic-uremic syndrome | PT/INR and PTT are normal, severe AKI |
Atypical hemolytic-uremic syndrome | PT/INR and PTT are normal, severe AKI |
HELLP syndrome | pregnancy |
Secondary | |
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 | |
Secondary hemolytic-uremic syndrome | most commonly from Streptococcus pneumoniae or influenza |
DIC | PT/INR and PTT are prolonged |
Malignancy | |
HIV |