Antiphospholipid antibodies (APLA) in immune thrombocytopenic purpura (ITP) and antiphospholipid syndrome (APS)

Thrombotic thrombocytopenic purpura with

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.