| Literature DB >> 32476842 |
Agnès Lohbrunner1, Laura Bitton2, Jacques Remy3, Benoit Wallaert1, Cécile Chenivesse1.
Abstract
Placental transmogrification of the lung is an extremely rare lung disease frequently associated with hamartomas or unilateral bullous emphysema. We report a case of placental transmogrification of the lung in a 44-year-old male who presented with bronchial infections, hyperlucent left lung and progressive cystic and micronodular unilateral interstitial lung disease. Because of interstitial lung disease progression over 13 years, a left pneumonectomy was performed. After a two-year follow-up, the patient was asymptomatic and did not exhibit any lung infections. No recurrence was observed on the right lung. (Sarcoidosis Vasc Diffuse Lung Dis 2017; 34: 188-190). Copyright:Entities:
Keywords: emphysema; interstitial lung disease; orphan disease; transmogrification
Year: 2017 PMID: 32476842 PMCID: PMC7170147 DOI: 10.36141/svdld.v34i2.5236
Source DB: PubMed Journal: Sarcoidosis Vasc Diffuse Lung Dis ISSN: 1124-0490 Impact factor: 0.670