Lohbrunner Agnès, Bitton Laura, Remy Jacques, Wallaert Benoit, Chenivesse Cécile
Centre Hospitalier Universitaire de Lille, Service de Pneumologie et Immuno-Allergologie, Centre de compétence des maladies pulmonaires rares et Université Lille 2, Lille F-50037, France.
Centre Hospitalier Universitaire de Lille, Service d'anatomie pathologique, F-50037, France.
Sarcoidosis Vasc Diffuse Lung Dis. 2017;34(2):188-190. doi: 10.36141/svdld.v34i2.5236. Epub 2017 Apr 28.
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. .
肺的胎盘异化是一种极其罕见的肺部疾病，常与错构瘤或单侧大疱性肺气肿相关。我们报告一例44岁男性肺的胎盘异化病例，该患者表现为支气管感染、左肺透亮度增加以及进行性囊性和微结节性单侧间质性肺病。由于间质性肺病病程长达13年，遂行左肺切除术。经过两年随访，患者无症状，未出现任何肺部感染。右肺未观察到复发情况。
