Department of Thoracic Surgery, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.
Department of Cardiovascular and Thoracic Surgery, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido, Japan.
Ann Thorac Cardiovasc Surg. 2022 Aug 20;28(4):298-301. doi: 10.5761/atcs.cr.20-00230. Epub 2020 Nov 3.
A 40-year-old woman with idiopathic pleuroparenchymal fibroelastosis (IPPFE) and flat chest underwent left single lung transplantation (SLT). Although she had developed over-systemic pulmonary arterial pressure (PAP) at transplantation, it was alleviated. However, her PAP gradually increased again. Her transplanted lung was well-inflated, but progression of fibrosis in her right native lung appeared to have caused a mediastinal shift, and her flat chest caused obstruction of the outflow tract of the pulmonary vein. She died of heart failure and associated infection 1.5 years after transplantation. An autopsy confirmed irreversible pulmonary arterial and venous changes in the transplanted lung, suggestive of chronic pressure overload. The flat chest associated with IPPFE can affect pulmonary circulation after SLT.
一位 40 岁的女性患有特发性胸膜肺弹力纤维增生症(IPPFE)和扁平胸,接受了左单肺移植(SLT)。尽管她在移植时已经出现了全身性肺动脉高压(PAP),但得到了缓解。然而,她的 PAP 逐渐再次升高。她的移植肺充气良好,但右侧原肺的纤维化进展似乎导致了纵隔移位,而扁平胸导致了肺静脉流出道阻塞。她在移植后 1.5 年因心力衰竭和相关感染而死亡。尸检证实移植肺存在不可逆的肺动脉和静脉变化,提示慢性压力超负荷。IPPFE 伴有的扁平胸可影响 SLT 后的肺循环。