[本月图片:青少年先天性肺气肿]。

Revue medicale de Liege Pub Date : 2025-04-01
Adrien Ruscher, Marc Dirix, Christian Cheping Simo, André Mulder, Matthieu Thimmesch
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引用次数: 0

摘要

先天性大叶性肺气肿是一种罕见的肺部畸形,通常在出生时或出生后几个月内出现呼吸窘迫。诊断通过影像学检查,如胸部x光片和胸部CT扫描,以及组织学检查来证实。早期肺叶切除术预后良好。在罕见的病例中,诊断是在青春期或成年期进行的,这与手术后肺恢复不完全有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Image of the month : congenital lobar emphysema in a teenager].

Congenital lobar emphysema is a rare pulmonary malformation that typically presents at birth or within the first few months of life as respiratory distress. Diagnosis is confirmed by imaging modalities such as chest X-rays and thoracic CT scans, and histological examination. Early lobectomy allows an excellent prognosis. In rare cases, the diagnosis is made during adolescence or adulthood, which is associated with incomplete pulmonary recovery following surgery.

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