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一例肺胎盘化生病例。

A case of pulmonary placental transmogrification.

作者信息

Jenkins Joanne M, Attia Rizwan Q, Green Anna, Cane Paul, Pilling John

机构信息

Kings College London, London UK.

Department of Cardiothoracic Surgery, Guy's and St. Thomas' Hospital, London, UK.

出版信息

Asian Cardiovasc Thorac Ann. 2016 Oct;24(8):811-813. doi: 10.1177/0218492316661462. Epub 2016 Jul 28.

Abstract

Pulmonary placental transmogrification is a rare lung lesion that microscopically resembles placenta with cystic spaces filled with papillary structures. Considered a histological variant of bullous emphysema, only 30 reported cases have been published in the world's literature. We report a rare case of pulmonary placental transmogrification in a 72-year-old man, in whom the clinical presentation of the disease mimicked lung carcinoma. Histopathology of the surgically resected segment showed a complex bulla with squamous metaplasia and placental transmogrification. Whilst rare, pulmonary placental transmogrification must be ruled out in all patients presenting with unilateral bullous emphysema, without known risk factors.

摘要

肺胎盘化生是一种罕见的肺部病变,在显微镜下类似于胎盘,有充满乳头状结构的囊腔。它被认为是大疱性肺气肿的一种组织学变体,世界文献中仅报道了30例。我们报告了一例72岁男性的罕见肺胎盘化生病例,该疾病的临床表现酷似肺癌。手术切除节段的组织病理学显示为一个复杂的大疱,伴有鳞状化生和胎盘化生。虽然罕见,但对于所有出现单侧大疱性肺气肿且无已知危险因素的患者,必须排除肺胎盘化生。

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