成人先天性肺气肿1例报告

M. Khalid, S. Saleemi, B. Khan
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引用次数: 8

摘要

先天性肺气肿(CLE)是一种非常罕见的疾病,其特征是受累肺叶过度膨胀,导致邻近正常肺组织和纵隔受压和移位。我们提出一个18岁的男性病例,他表现出急性支气管炎的症状,常规胸部x线检查导致怀疑CLE,并通过先进的成像技术证实。我们回顾了文献来讨论这种非常罕见的疾病,它几乎总是出现在生命的早期,只有少数病例在成人中报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital lobar emphysema in adult: A rare case report

Congenital lobar emphysema (CLE) is a very rare disease characterized by over-distension of the affected lobe leading to compression and displacement of adjacent normal lung tissue and mediastinum. We present a case of 18 years old male who presented with symptoms of acute bronchitis and routine chest X-ray led to the suspicion of CLE which was confirmed by advance imaging techniques. We reviewed the literature to discuss this very rare illness which almost always present in early years of life and only a handful cases are reported in adults.

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