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von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura

✍ Scribed by Flora Peyvandi; Silvia Ferrari; Silvia Lavoretano; Maria Teresa Canciani; Pier Mannuccio Mannucci

Book ID: 108672898
Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 145 KB
Volume: 127
Category: Article
ISSN: 0007-1048
DOI: 10.1111/j.1365-2141.2004.05217.x

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## Abstract Arterial thrombotic events, thrombocytopenia, and hemolytic anemia with schistocytes may be encountered in the setting of both thrombotic thrombocytopenic purpura (TTP) and primary antiphospholipid syndrome (APS). We report 2 cases of TTP occurring in patients with definite primary APS.