一例婴幼儿急性呼吸道感染所致单侧肺发育不全。

IF 0.7 Q4 PEDIATRICS
S Aimée Kissou, Souleymane B W Adjaba, Jacqueline Tamini, Hélène Traore
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引用次数: 0

摘要

肺发育不全是一种罕见的先天性异常,原因不明,包括肺实质、支气管和血管的完全缺失。它可能与其他畸形有关,也可能与其他畸形无关。作者报告一例右肺发育不全诊断在一个四个月大的婴儿谁没有以前的病理病史和生长良好。发现的情况是在感染发作期间呼吸窘迫。在标准的胸部x光检查中,诊断是可疑的,在胸部CT扫描中得到证实。没有其他相关的缺陷。抗生素治疗后进化良好。虽然双侧肺发育不全与生活不相容,但单侧形式可能直到成年后才被发现。预后主要取决于相关畸形的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unilateral Pulmonary Agenesis about a Case Revealed by an Acute Respiratory Infection in a Young Infant.

Unilateral Pulmonary Agenesis about a Case Revealed by an Acute Respiratory Infection in a Young Infant.

Unilateral Pulmonary Agenesis about a Case Revealed by an Acute Respiratory Infection in a Young Infant.

Pulmonary agenesis is a rare congenital anomaly of unknown cause, consisting of a complete absence of the lung parenchyma, bronchi, and vascularization. It may or not be associated with other malformations. The authors report a case of right pulmonary agenesis diagnosed in a four-month-old infant who had no previous pathological history and was growing well. The circumstance of discovery was respiratory distress during an infectious episode. The diagnosis was suspected on a standard chest X-ray and confirmed on a chest CT scan. There are no other associated defects. The evolution was good after antibiotic therapy. While bilateral pulmonary agenesis is incompatible with life, the unilateral form may remain unrecognized until adulthood. The prognosis depends mainly on the importance of the associated malformations.

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来源期刊
自引率
11.10%
发文量
48
审稿时长
13 weeks
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