Division of Laboratory and Genomic Medicine, Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Division of Hematology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Thorax. 2018 May;73(5):489-492. doi: 10.1136/thoraxjnl-2017-211121. Epub 2018 Jan 30.
Familial pulmonary fibrosis is associated with loss-of-function mutations in telomerase reverse transcriptase () and short telomeres. Interstitial lung diseases have become the leading indication for lung transplantation in the USA, and recent data indicate that pathogenic mutations in telomerase may cause unfavourable outcomes following lung transplantation. Although a rare occurrence, solid organ transplant recipients who develop acute graft-versus-host disease (GVHD) have very poor survival. This case report describes the detection of a novel mutation in in a patient who had lung transplantation for familial pulmonary fibrosis and died from complications of acute GVHD.
家族性肺纤维化与端粒酶逆转录酶 () 的功能丧失性突变和端粒缩短有关。间质性肺疾病已成为美国肺移植的主要适应证,最近的数据表明端粒酶的致病性突变可能导致肺移植后预后不良。尽管这种情况很少见,但发生急性移植物抗宿主病 (GVHD) 的实体器官移植受者的生存率非常低。本病例报告描述了一名因家族性肺纤维化而行肺移植并死于急性 GVHD 并发症的患者中端粒酶中一个新突变的检测。