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原发性干燥综合征、肺囊性疾病和边缘区淋巴瘤患者成功接受利妥昔单抗治疗:基于病例的综述。

A patient with primary Sjogren's syndrome, cystic lung disease, and MALT lymphoma treated successfully with rituximab: a case-based review.

机构信息

Division of Rheumatology, University of Southern California, Los Angeles, CA, USA.

出版信息

Clin Rheumatol. 2020 Apr;39(4):1357-1362. doi: 10.1007/s10067-019-04886-7. Epub 2019 Dec 20.

Abstract

Primary Sjogren's syndrome (pSS) can have a myriad of presentations, ranging from mild xerostomia to more diffuse systemic involvement. It is well established that pSS is associated with a variety of pulmonary pathologies, and it is also known that pSS patients are at higher risk for lymphoma development. Here, we present an unusual case of a woman with primary Sjogren's syndrome who had both diffuse cystic lung disease as well as extranodal MALT lymphoma, successfully treated for both conditions with the CD-20 monoclonal antibody rituximab.

摘要

原发性干燥综合征(pSS)的表现多种多样,从轻度口干到更广泛的全身受累都有可能。众所周知,pSS 与多种肺部疾病有关,而且 pSS 患者发生淋巴瘤的风险也更高。在这里,我们报告了一例不常见的女性原发性干燥综合征病例,该患者同时患有弥漫性囊性肺疾病和结外黏膜相关淋巴组织(MALT)淋巴瘤,用 CD-20 单克隆抗体利妥昔单抗成功治疗了这两种疾病。

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