Thrombotic microangiopathy: Difference between revisions

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|[[Hemolytic-uremic syndrome]]
|[[Hemolytic-uremic syndrome]]
|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]]
|PT/INR and PTT are normal
|PT/INR and PTT are normal, severe AKI
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|[[HELLP syndrome]]
|[[HELLP syndrome]]
|pregnancy
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! colspan="2" |Secondary
! colspan="2" |Secondary

Latest revision as of 11:26, 19 March 2024

Disease Clinical Clues
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