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特发性胸膜肺实质纤维弹性组织增生症:在利雅得法赫德国王专科医院及研究中心成功接受肺移植治疗的首例病例。

Idiopathic pleuroparenchymal fibroelastosis: The first case to be managed with a successful lung transplant at King Faisal Specialist Hospital and Research Center, Riyadh.

作者信息

Aljefri Nour Abdullah, Abothenain Fayha Farraj, Hussein Ahmed Mohamed, Saleh Waleed, Alkattan Khaled, Mohammed Shamayel Faheem, Alhajji Mohammed

机构信息

Alfaisal Medical School, Alfaisal University, Riyadh, Saudi Arabia.

Section of Thoracic Surgery, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

出版信息

Ann Thorac Med. 2019 Jan-Mar;14(1):94-98. doi: 10.4103/atm.ATM_106_18.

DOI:10.4103/atm.ATM_106_18
PMID:30745942
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6341862/
Abstract

Idiopathic Pleuro-Parenchymal Fibroelsatosis (PPFE) is a rare, progressive and recently recognized subtype of idiopathic interstitial lung disease with no recorded successful treatment other than lung transplant. We report a case of idiopathic pleuroparenchymal fibroelastosis from the Middle East, managed successfully by bilateral lung transplant performed on a 26 year old Saudi male.

摘要

特发性胸膜-肺实质纤维弹性组织增生症(PPFE)是一种罕见的、进行性的且最近才被认识的特发性间质性肺疾病亚型,除肺移植外尚无成功治疗的记录。我们报告一例来自中东的特发性胸膜-肺实质纤维弹性组织增生症病例,该病例通过对一名26岁沙特男性进行双侧肺移植而成功治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/79d7a4845d98/ATM-14-94-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/dcd8797fdabd/ATM-14-94-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/a418f8073973/ATM-14-94-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/e6941ffeecb7/ATM-14-94-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/bc1fb025ea5a/ATM-14-94-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/14bf4c9b9bec/ATM-14-94-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/79d7a4845d98/ATM-14-94-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/dcd8797fdabd/ATM-14-94-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/a418f8073973/ATM-14-94-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/e6941ffeecb7/ATM-14-94-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/bc1fb025ea5a/ATM-14-94-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/14bf4c9b9bec/ATM-14-94-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca1/6341862/79d7a4845d98/ATM-14-94-g007.jpg

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本文引用的文献

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A CARE-compliant case report: Lung transplantation for a Chinese young man with idiopathic pleuroparenchymal fibroelastosis.一份符合CARE标准的病例报告:为一名患有特发性胸膜肺实质纤维弹性组织增生症的中国年轻男子进行肺移植
Medicine (Baltimore). 2017 May;96(19):e6900. doi: 10.1097/MD.0000000000006900.
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Pleuroparenchymal Fibroelastosis of the Lung: A Review.肺胸膜实质纤维弹性组织增生症:综述
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Idiopathic pleuroparenchymal fibroelastosis - A rare idiopathic interstitial pneumonia.
一例特发性胸膜肺实质纤维弹性组织增生症尸检病例,伴有左侧声带麻痹且无急性加重情况下病情迅速恶化。
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特发性胸膜肺实质纤维弹性组织增生症——一种罕见的特发性间质性肺炎。
Respir Med Case Rep. 2015 Nov 22;17:8-11. doi: 10.1016/j.rmcr.2015.11.004. eCollection 2016.
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A Patient with Idiopathic Pleuroparenchymal Fibroelastosis Showing a Sustained Pulmonary Function due to Treatment with Pirfenidone.一名特发性胸膜肺实质纤维弹性组织增生症患者因使用吡非尼酮治疗而肺功能持续改善。
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Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics.胸膜实质纤维弹性组织增生症:其临床特征
Curr Respir Med Rev. 2013 Jun;9(4):299-237. doi: 10.2174/1573398X0904140129125307.
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An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias.美国胸科学会/欧洲呼吸学会官方声明:特发性间质性肺炎的国际多学科分类的更新。
Am J Respir Crit Care Med. 2013 Sep 15;188(6):733-48. doi: 10.1164/rccm.201308-1483ST.
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BMC Pulm Med. 2012 Dec 5;12:72. doi: 10.1186/1471-2466-12-72.
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Idiopathic pleuroparenchymal fibroelastosis: description of a novel clinicopathologic entity.特发性胸膜肺实质纤维弹性组织增生症:一种新型临床病理实体的描述。
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