首页> 外文期刊>Respiratory Medicine Case Reports >Combination of pleuroparenchymal fibroelastosis with non-specific interstitial pneumonia and bronchiolitis obliterans as a complication of hematopoietic stem cell transplantation — Clues to a potential mechanism
【24h】

Combination of pleuroparenchymal fibroelastosis with non-specific interstitial pneumonia and bronchiolitis obliterans as a complication of hematopoietic stem cell transplantation — Clues to a potential mechanism

机译:胸膜实质性纤维弹性增生与非特异性间质性肺炎和闭塞性细支气管炎的合并,作为造血干细胞移植的并发症—线索可能存在

获取原文
       

摘要

Pleuroparenchymal fibroelastosis (PPFE) is a newly described entity of interstitial lung disease, which has been recently recognized as a rare complication of bone marrow transplantation. We report a case of 30-year-old man who developed a unique combination of pleuroparenchymal fibroelastosis with cellular and fibrotic non-specific interstitial pneumonia (NSIP) and bronchiolitis obliterans (BO) sixteen years after hematopoietic stem cell transplantation. Histological examination revealed almost exclusive infiltration of CD3-positive T lymphocytes associated with lymphoepithelial lesions and multi-focal denudation of covering epithelial cells in all components. This case suggests PPFE, NSIP, and BO might be conditions of the same spectrum, pathogenetically related to chronic graft-versus-host disease. Immunostaining for CD3 and CD20 in transbronchial lung biopsies may be helpful for identifying graft-versus-host-driven interstitial lung disease.
机译:胸膜实质纤维弹性增生(PPFE)是间质性肺病的最新描述,最近被认为是骨髓移植的一种罕见并发症。我们报告了一名30岁男子的案例,该病人在造血干细胞移植后十六年发展了胸膜实质纤维弹性增生与细胞和纤维化非特异性间质性肺炎(NSIP)和闭塞性细支气管炎(BO)的独特结合。组织学检查显示与淋巴上皮病变相关的CD3阳性T淋巴细胞几乎全部浸润,并且所有成分的覆盖上皮细胞均多灶性剥脱。这种情况表明PPFE,NSIP和BO可能是同一频谱的疾病,在病原学上与慢性移植物抗宿主病有关。经支气管肺活检中CD3和CD20的免疫染色可能有助于鉴定移植物抗宿主驱动的间质性肺疾病。

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