婴儿先天性肺气道畸形和支气管肺隔离——罕见的诊断

Joana Cachão, Isabel Raminhos, J. Martins, I. Bravio
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引用次数: 0

摘要

本文描述了一个两个月大的女婴复发性呼吸道感染的情况下,入院儿科急诊科生产咳嗽,呼吸窘迫,发烧。胸片显示左肺野不均匀低透明影及对侧纵隔偏曲。血管断层扫描显示双侧支气管肺隔离和全身血管有助于区域冲洗。患者接受血管闭塞和涂漆,左下叶切除术和右下叶切除术。组织学检查证实左肺为肺叶内支气管肺隔离及2型先天性肺气道畸形,右肺为肺叶外支气管肺隔离。在本报告中,作者打算强调临床怀疑婴儿先天性异常复发性呼吸道感染的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital pulmonary airway malformation and bronchopulmonary sequestration in infants - a rare diagnosis
Herein is described the case of a two-month-old female infant with recurrent respiratory infections, admitted to the Pediatric Emergency Department with productive cough, respiratory distress, and fever. Chest radiography showed an heterogenous hypotransparent image in the left pulmonary field and contralateral deviation of the mediastinum. Angiotomography revealed bilateral bronchopulmonary sequestration and a systemic vessel contributing to area irrigation. The patient was submitted to vessel occlusion and lacquering, left inferior lobectomy, and resection of a right lower lobe segment. Histological examination confirmed intralobar bronchopulmonary sequestration and type 2 congenital pulmonary airway malformation in the left lung, and extralobar bronchopulmonary sequestration in the right lung.With this report, the authors intend to emphasize the importance of clinical suspicion of congenital anomalies in infants with recurrent respiratory infections.
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