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[先天性肺叶气肿]

[Congenital lobar emphysema].

作者信息

Omerctahić-Dizdarević Aida, Saracević Ediba, Jonuzi Fedzet, Misanović Verica, Anić Dusko, Kalkan Ismeta, Cengić Amra

机构信息

Pedijatrijska Klinika, Kliniki Centar Univerziteta Sarajevu.

出版信息

Med Arh. 2005;59(2):113-4.

Abstract

BACKGROUND

Congenital lobar emphysema is characterized by overinflation of pulmonary lobe and is caused by localised bronchial obstruction. The disease may result in severe respiratory distress in early infancy.

METHODS

Records of children, with congenital lobar emphysema, who were treated at our department between 1997-2003, were reviewed.

RESULTS

Three males, aged 16 days till 1 year, were diagnosticed as congenital lobar emphysema. Presenting symptoms were dyspnea in 2 patients, cyanosis in 2 patients, wheesing in 2 patients, recurrent respiratory tract infection in 2 patients. Chest x rays and computerized tomography scans showed hyperinflation of the affected lobe in all patients. The affected sites were left upper lobe in 2 patients and right upper lobe in 1 patient. All patients underwent lobectomy.

CONCLUSION

It is necessary to suspect on this uncommon anomaly in early infancy. The diagnosis was established by chest x rays and CT scans. Intensive therapy and urgent lobectomy, in severe respiratory distress, are condition for successfully treatment.

摘要

背景

先天性肺叶气肿的特征是肺叶过度充气,由局部支气管阻塞引起。该疾病可能在婴儿早期导致严重的呼吸窘迫。

方法

回顾了1997年至2003年在我科接受治疗的先天性肺叶气肿患儿的记录。

结果

3名男性,年龄从16天至1岁,被诊断为先天性肺叶气肿。主要症状为2例呼吸困难、2例发绀、2例喘息、2例反复呼吸道感染。胸部X线和计算机断层扫描显示所有患者患叶均有过度充气。受累部位2例为左上叶,1例为右上叶。所有患者均接受了肺叶切除术。

结论

在婴儿早期有必要怀疑这种不常见的异常情况。通过胸部X线和CT扫描确诊。对于严重呼吸窘迫的患者,强化治疗和紧急肺叶切除术是成功治疗的条件。

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