首页> 外文期刊>Respiratory Medicine Case Reports >A case of spontaneous regression of pulmonary mucosa-associated lymphoid tissue (MALT) type lymphoma with Sj?gren's syndrome treated with methotrexate for rheumatoid arthritis
【24h】

A case of spontaneous regression of pulmonary mucosa-associated lymphoid tissue (MALT) type lymphoma with Sj?gren's syndrome treated with methotrexate for rheumatoid arthritis

机译:甲氨蝶呤治疗类风湿性关节炎合并肺粘膜相关淋巴样组织(MALT)型淋巴瘤合并干燥综合征1例

获取原文
获取外文期刊封面目录资料

摘要

A 72-year-old man who had suffered from rheumatoid arthritis (RA) and Sj?gren's syndrome (Sjs) since he was 66 years of age had been treated with methotrexate (MTX) for six years. He presented with a cough, sputum and dyspnea on exertion, and computed tomography findings showed multiple ground-glass opacities in both of his lungs. A biopsy of the lungs revealed low-grade mucosa-associated lymphoid tissue (MALT) type B-cell non-Hodgkin's lymphoma. Spontaneous complete remission of the lymphoma was achieved six months after withdrawing immune suppression with MTX. To our knowledge, no previous cases of spontaneous regression of pulmonary MALT-type lymphoma with Sjs treated with MTX for RA have been reported. Patients on MTX who are being treated for RA should be carefully monitored, especially when they have been diagnosed with coexistent Sjs.
机译:一名自66岁起就患有类风湿关节炎(RA)和干燥综合征(Sjs)的72岁男子接受了甲氨蝶呤(MTX)的治疗6年。他劳累时出现咳嗽,咳嗽和呼吸困难,计算机断层扫描发现他的两个肺部都出现多个毛玻璃状混浊。肺活检显示低级别的黏膜相关淋巴样组织(MALT)B细胞非霍奇金淋巴瘤。停用MTX免疫抑制后六个月,淋巴瘤自然自发缓解。据我们所知,以前没有报道过用MTX治疗RA的Sjs引起的肺MALT型淋巴瘤自发消退的病例。应该仔细监测正在接受RA治疗的MTX上的患者,尤其是当他们被诊断患有共存Sjs时。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号