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Thrombotic thrombocytopenic purpura in IgG4-related disease with severe deficiency of ADAMTS-13 activity and IgG4 autoantibody against ADAMTS-13

✍ Scribed by Takako Saeki; Tomoyuki Ito; Akira Youkou; Hajime Ishiguro; Naoko Sato; Hajime Yamazaki; Tadashi Koike; Hiroyo Kourakata; Silvia Ferrari; Friedrich Scheiflinger; Ichiei Narita

Publisher: Wiley (John Wiley & Sons)
Year: 2011
Tongue: English
Weight: 248 KB
Volume: 63
Category: Article
ISSN: 2151-464X
DOI: 10.1002/acr.20484

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Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome

✍ Zahir Amoura; Nathalie Costedoat-Chalumeau; Agnès Veyradier; Martine Wolf; Pasca 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 54 KB 👁 1 views

## 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.