| Literature DB >> 32231537 |
Bahjat Azrieh1, Arwa Alsaud1, Khaldun Obeidat1, Amr Ashour1, Seham Elebbi1, Shehab F Mohamed2, Mohamed Adel Abdelaty2, Abdelraouf Akkari2, Abdurrahman Ali Elbuzidi2, Mohamed A Yassin2.
Abstract
Thrombotic thrombocytopenic purpura (TTP) is a rare, serious, life-threatening disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, and hypercoagulability. The etiology is a deficiency of ADAMTS13 which is usually caused by acquired antibodies. Plasma exchange and steroids is the standard of care in the treatment of TTP. However, there are refractory cases of TTP which require further management. Rituximab appears to be a safe and effective therapy for refractory and relapsing TTP. Here we report a challenging case of TTP that responded to treatment with rituximab twice weekly. According to our knowledge, rituximab twice weekly has never been used for TTP before.Entities:
Keywords: Platelet disorder; Refractory disease; Relapse; Rituximab; Thrombocytopenia; Thrombotic thrombocytopenic purpura
Year: 2020 PMID: 32231537 PMCID: PMC7098356 DOI: 10.1159/000505236
Source DB: PubMed Journal: Case Rep Oncol ISSN: 1662-6575