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先天性大叶性肺气肿:一名2个月大婴儿的诊断难题及进行性呼吸窘迫的病因

Congenital lobar emphysema: a diagnostic challenge and cause of progressive respiratory distress in a 2 month-old infant.

作者信息

Idro Richard I, Kisembo Harriet, Mugisa Didas, Bulamu Alfred

机构信息

Department of Paediatrics and Child Health, Mulago Hospital, P O Box 7051, Kampala, Uganda.

出版信息

Afr Health Sci. 2002 Dec;2(3):121-3.

Abstract

Congenital lobar emphysema (CLE) is a rare congenital abnormality characterized by over inflation of a pulmonary lobe. It often presents a diagnostic and therapeutic dilemma. No case has been described in Uganda in the previous 10 years. We describe a case of a 2 months old infant who presented with severe respiratory distress. A diagnosis of congenital left upper lobar emphysema was established on diagnostic imaging. Both his vascular anatomy and the bronchial wall were normal. He improved dramatically after surgery. The SaO2 normalized within 12 hours of Surgery (lobectomy) and the postoperative period was uneventful.

摘要

先天性肺叶气肿(CLE)是一种罕见的先天性异常,其特征为肺叶过度充气。它常常带来诊断和治疗上的难题。在过去10年里,乌干达尚未有相关病例报道。我们描述了一例2个月大的婴儿,该婴儿出现严重呼吸窘迫。经诊断性影像学检查确诊为先天性左上叶气肿。其血管解剖结构和支气管壁均正常。手术后他的病情显著改善。术后12小时内(肺叶切除术)血氧饱和度(SaO2)恢复正常,术后恢复过程顺利。

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