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Likely causes of microangiopathic hemolytic anemia and thrombocytopenia according to presenting findings

Likely causes of microangiopathic hemolytic anemia and thrombocytopenia according to presenting findings
No clinical finding is completely sensitive or specific for a specific primary TMA diagnosis. Refer to UpToDate for an approach to the patient with a suspected thrombotic microangiopathy for further information about specific disorders.
DIC: disseminated intravascular coagulation; HELLP: hemolysis, elevated liver function tests, low platelets; HUS: hemolytic-uremic syndrome; MAHA: microangiopathic hemolytic anemia; TMA: thrombotic microangiopathy; TTP: thrombotic thrombocytopenic purpura.
Adapted from: George JN, Nester CM. Syndromes of thrombotic microangiopathy. N Eng J Med 2014; 371:654.
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