Pleuroparenchymal fibroelastosis (PPFE) treated with lung transplantation and review of the literature

被引:10
作者
Ali, Muhammad Sajawal [1 ]
Ramalingam, Vijaya Sivalingam [1 ]
Haasler, George [2 ]
Presberg, Kenneth [1 ]
机构
[1] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Cardiothorac Surg, Milwaukee, WI 53226 USA
关键词
interstitial lung disease; cardiothoracic surgery; transplantation; HEMATOPOIETIC STEM-CELL; COMPLICATION; SECONDARY; FEATURES; FIBROSIS;
D O I
10.1136/bcr-2019-229402
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 26-year-old woman presented with a 15-year history of non-progressive dyspnoea. Chest imaging showed bilateral apical pleural and parenchymal scarring, pleural thickening and bronchiectasis. Pulmonary function tests showed a moderate restrictive defect. Non-invasive workup was non-revealing; therefore, the patient was referred for video-assisted thoracic surgery and lung biopsy. Histopathology revealed pleural thickening and, subpleural parenchymal fibrosis and elastic tissue deposition. Lung parenchyma further away from the pleura was well preserved. Based on these findings, the patient was diagnosed with pleuroparenchymal fibroelastosis (PPFE). Since PPFE is a progressive disorder without effective medical therapies, and given our patient's worsening symptoms, she underwent bilateral lung transplantation. It has been almost 4years since the lung transplantation, our patient continues to do well. To the best of our knowledge, to date, this is the longest follow-up reported for a PPFE patient undergoing lung transplantation.
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页数:5
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