Rubenstein Elyse, Arkfeld Daniel G, Metyas Samy, Shinada Shuntaro, Ehresmann Sonya, Liebman Howard A
Division of Rheumatology and Division of Hematology, Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, 90033, USA.
J Rheumatol. 2006 Feb;33(2):355-7.
Antiphospholipid syndrome (APS) and catastrophic antiphospholipid syndrome (CAPS) can be challenging to treat. As they are rare, clinicians are not often exposed to these complex diseases. For the patient resistant to standard treatments new therapeutic directions can be perplexing, especially in the context of ongoing thromboses and bleeding episodes. We describe 3 patients, 2 with APS and one with CAPS, resistant to conventional medications, who responded to treatment with rituximab, an anti-CD20 monoclonal antibody. Since rituximab infusion, all the patients have had stable platelet counts and no further episodes of bleeding or thromboses.
抗磷脂综合征(APS)和灾难性抗磷脂综合征(CAPS)的治疗可能具有挑战性。由于它们较为罕见,临床医生并不常接触到这些复杂疾病。对于对标准治疗耐药的患者,新的治疗方向可能令人困惑,尤其是在持续发生血栓形成和出血事件的情况下。我们描述了3例患者,其中2例为APS,1例为CAPS,他们对传统药物耐药,但对使用抗CD20单克隆抗体利妥昔单抗治疗有反应。自输注利妥昔单抗以来,所有患者的血小板计数均保持稳定,且未再发生出血或血栓形成事件。