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首例两名溃疡性结肠炎患者发生典型血栓性血小板减少性紫癜,经药物治疗和血浆置换成功治愈。

First two patients with ulcerative colitis who developed classical thrombotic thrombocytopenic purpura successfully treated with medical therapy and plasma exchange.

作者信息

Baron Beverly W, Jeon Hye-Ran, Glunz Catherine, Peterson Amy, Cohen Russell, Hanauer Stephen, Rubin David, Hart John, Baron Joseph M

机构信息

Department of Pathology, The University of Chicago, Chicago, Illinois, USA.

出版信息

J Clin Apher. 2002;17(4):204-6. doi: 10.1002/jca.10037.

Abstract

The association of ulcerative colitis (UC) and thrombotic thrombocytopenic purpura (TTP) is rare. Only one prior patient with these two syndromes has been reported in the literature. In that case, splenectomy and proctectomy were performed to control the symptoms of TTP. We present two patients with UC who developed TTP and were successfully treated with multiple plasma exchanges (PEXs) in conjunction with medical therapy without the necessity for surgical intervention. Acquired TTP may be another extraintestinal autoimmune feature of UC. TTP in association with UC may be refractory to high-dose steroids and PEX, possibly requiring vincristine and splenectomy, as in the one previously reported case, to achieve remission.

摘要

溃疡性结肠炎(UC)与血栓性血小板减少性紫癜(TTP)的关联较为罕见。文献中仅报道过一例同时患有这两种综合征的患者。在该病例中,实施了脾切除术和直肠切除术以控制TTP的症状。我们报告了两名患有UC并发展为TTP的患者,他们通过多次血浆置换(PEX)联合药物治疗成功治愈,无需手术干预。获得性TTP可能是UC的另一种肠外自身免疫特征。与UC相关的TTP可能对大剂量类固醇和PEX治疗无效,可能需要像之前报道的病例那样使用长春新碱并进行脾切除术才能实现缓解。

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