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肺移植后限制性移植物综合征的特征是胸膜肺纤维弹性组织增生。

Restrictive allograft syndrome post lung transplantation is characterized by pleuroparenchymal fibroelastosis.

机构信息

Laboratory Medicine Program, University Health Network, Toronto, ON, Canada.

出版信息

Mod Pathol. 2013 Mar;26(3):350-6. doi: 10.1038/modpathol.2012.171. Epub 2012 Sep 28.

Abstract

We previously described restrictive allograft syndrome as a form of chronic lung allograft dysfunction, demonstrating restrictive pulmonary function decline. However, the histopathological correlates of restrictive allograft syndrome have yet to be satisfactorily described. We hypothesized that pulmonary pleuroparenchymal fibroelastosis, as has recently been described in bone marrow transplant recipients, may also be present in the lungs of patients with restrictive allograft syndrome. Retrospective review of 493 patients who underwent lung transplantation between 1 January 1996 and 30 June 2009, was conducted. Out of 47 patients with clinical features of restrictive allograft syndrome, 16 had wedge biopsy, re-transplant lung explant, or autopsy lung specimens available for review. All lungs showed varying degrees of pleural fibrosis. Fifteen of 16 showed parenchymal fibroelastosis, characterized by hypocellular collagen deposition with preservation and thickening of the underlying alveolar septal elastic network. The fibroelastosis was predominantly subpleural in distribution, with some cases also showing centrilobular and paraseptal distribution. A sharp demarcation was often seen between areas of fibroelastosis and unaffected lung parenchyma, with fibroblastic foci often present at this interface. Concurrent features of obliterative bronchiolitis were present in 14 cases. Another common finding was the presence of diffuse alveolar damage (13 cases), usually in specimens obtained <1 year after clinical onset of restrictive allograft syndrome. The single specimen in which fibroelastosis was not identified was obtained before the clinical onset of chronic lung allograft dysfunction, and showed features of diffuse alveolar damage. In conclusion, pleuroparenchymal fibroelastosis is a major histopathologic correlate of restrictive allograft syndrome, and was often found concurrently with diffuse alveolar damage. Our findings support a temporal sequence of diffuse alveolar damage followed by the development of pleuroparenchymal fibroelastosis in the histopathologic evolution of restrictive allograft syndrome.

摘要

我们之前将限制性移植物综合征描述为一种慢性肺移植物功能障碍的形式,表现为限制性肺功能下降。然而,限制性移植物综合征的组织病理学相关性尚未得到满意描述。我们假设,最近在骨髓移植受者中描述的肺胸膜实质纤维弹性化,也可能存在于限制性移植物综合征患者的肺部。对 1996 年 1 月 1 日至 2009 年 6 月 30 日期间接受肺移植的 493 名患者进行了回顾性审查。在 47 名具有限制性移植物综合征临床特征的患者中,有 16 名患者的楔形活检、再次移植的肺移植标本或尸检肺标本可供审查。所有肺均显示不同程度的胸膜纤维化。16 例中有 15 例显示实质纤维弹性化,其特征为细胞减少的胶原沉积,同时保持并增厚了基础肺泡间隔弹性网络。纤维弹性化主要分布于胸膜下,有些病例还显示小叶中心和隔旁分布。纤维弹性化和未受影响的肺实质之间通常有明显的界限,在该界面处常存在成纤维细胞灶。14 例存在闭塞性细支气管炎的同时性特征。另一个常见的发现是弥漫性肺泡损伤(13 例),通常在限制性移植物综合征临床发病后 <1 年内获得的标本中。唯一未识别出纤维弹性化的标本是在慢性肺移植物功能障碍临床发病前获得的,表现为弥漫性肺泡损伤的特征。总之,胸膜实质纤维弹性化是限制性移植物综合征的主要组织病理学相关性,通常与弥漫性肺泡损伤同时存在。我们的发现支持在限制性移植物综合征的组织病理学演变中,弥漫性肺泡损伤先于胸膜实质纤维弹性化发生的时间顺序。

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