Autopsy findings in a case of idiopathic pleuroparenchymal fibroelastosis: A rare entity with review of literature

Anjali Ahalawat, R. Verma, R. Kalra, Pinki Tomer, Sunita Singh
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引用次数: 0

Abstract

Idiopathic pleuroparenchymal fibroelastosis is a rare idiopathic interstitial pneumonia which mainly affects the upper lobe of lungs resulting in intra alveolar fibrosis, elastosis and visceral pleural fibrosis. For definite diagnosis, radiographic findings as well as histopathology findings are required. The overlap with interstitial lung diseases seen usually, makes it challenging to diagnose. There are no guidelines available for the diagnosis and appropriate management of this disease and only a few cases reported in the literature. We report a case of pleuroparenchymal fibroelastosis in autopsy in a 32-year-old female who allegedly died of heart failure with review of literature.
特发性胸膜实质纤维弹性病的尸检结果:一个罕见的实体与文献复习
特发性胸膜实质纤维弹性增生症是一种罕见的特发性间质性肺炎,主要累及肺上叶,导致肺泡内纤维化、弹性增生和内脏性胸膜纤维化。为了明确诊断,需要影像学检查和组织病理学检查。通常与间质性肺疾病重叠,使其难以诊断。对于这种疾病的诊断和适当的管理没有指导方针,文献中只有少数病例报道。我们报告一例胸膜实质纤维弹性病在尸检在一个32岁的女性谁据称死于心力衰竭与文献回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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