Congenital Bronchial Atresia: Diagnosis and Treatment

<p>This study aimed to retrospectively summarize the clinical signs, diagnosis, and treatment of congenital bronchial atresia (CBA) in 12 patients. Chest radiographs and computed tomographic (CT) images of 12 patients with CBA treated in the Chinese People's Liberation Army General Hospit...

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Main Author: Yuqi Wang, Weimin Dai, Yu'e Sun, Xiangyang Chu, Bo Yang, Ming Zhao
Format: Article
Language:English
Published: Ivyspring International Publisher 2012-01-01
Series:International Journal of Medical Sciences
Online Access:http://www.medsci.org/v09p0207.htm
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spelling doaj-99ce55443a584be9838c7891bac63f432020-11-24T22:26:33ZengIvyspring International PublisherInternational Journal of Medical Sciences1449-19072012-01-0193207212Congenital Bronchial Atresia: Diagnosis and TreatmentYuqi Wang, Weimin Dai, Yu'e Sun, Xiangyang Chu, Bo Yang, Ming Zhao<p>This study aimed to retrospectively summarize the clinical signs, diagnosis, and treatment of congenital bronchial atresia (CBA) in 12 patients. Chest radiographs and computed tomographic (CT) images of 12 patients with CBA treated in the Chinese People's Liberation Army General Hospital were reviewed. Analysis of chest radiographs revealed ten patients had hilar mass-like shadows and two had pneumonia-like shadows; most patients (n = 8) showed hyperlucency of the peripheral lung fields. CT revealed a mucocele in all the patients (n = 12); the mucoceles were round in four patients and club-like in eight. In 80% of the cases (n = 10), associated anomalies, including occlusions of the bronchus central to the mucocele, emphysematous changes of the peripheral lung fields, bronchogenic cyst, and anomalous branching of the bronchial tree and vascular structure were observed. CBA was detected in the right lobe in eight patients and the left lobe in the remaining four. No surgical intervention was performed in 5 CBA patients and the remaining 7 patients underwent surgery, including lobectomy in 5 patients and local resection in 2 patients. Among these 7 patients, 3 had a preoperative diagnosis of malignant disease, and the remaining 4 had severe clinical symptoms that could not be effectively treated by medicines. All patients were followed up, and none experienced obvious discomfort. CBA is a relatively rare and benign malformation disease. Chest CT is the procedure of choice for diagnosis. The presence of a bronchocele and surrounding emphysematous changes are typical radiologic findings in CBA. Surgery should be reserved only for patients with serious complications secondary to the atretic bronchus.</p>http://www.medsci.org/v09p0207.htm
collection DOAJ
language English
format Article
sources DOAJ
author Yuqi Wang, Weimin Dai, Yu'e Sun, Xiangyang Chu, Bo Yang, Ming Zhao
spellingShingle Yuqi Wang, Weimin Dai, Yu'e Sun, Xiangyang Chu, Bo Yang, Ming Zhao
Congenital Bronchial Atresia: Diagnosis and Treatment
International Journal of Medical Sciences
author_facet Yuqi Wang, Weimin Dai, Yu'e Sun, Xiangyang Chu, Bo Yang, Ming Zhao
author_sort Yuqi Wang, Weimin Dai, Yu'e Sun, Xiangyang Chu, Bo Yang, Ming Zhao
title Congenital Bronchial Atresia: Diagnosis and Treatment
title_short Congenital Bronchial Atresia: Diagnosis and Treatment
title_full Congenital Bronchial Atresia: Diagnosis and Treatment
title_fullStr Congenital Bronchial Atresia: Diagnosis and Treatment
title_full_unstemmed Congenital Bronchial Atresia: Diagnosis and Treatment
title_sort congenital bronchial atresia: diagnosis and treatment
publisher Ivyspring International Publisher
series International Journal of Medical Sciences
issn 1449-1907
publishDate 2012-01-01
description <p>This study aimed to retrospectively summarize the clinical signs, diagnosis, and treatment of congenital bronchial atresia (CBA) in 12 patients. Chest radiographs and computed tomographic (CT) images of 12 patients with CBA treated in the Chinese People's Liberation Army General Hospital were reviewed. Analysis of chest radiographs revealed ten patients had hilar mass-like shadows and two had pneumonia-like shadows; most patients (n = 8) showed hyperlucency of the peripheral lung fields. CT revealed a mucocele in all the patients (n = 12); the mucoceles were round in four patients and club-like in eight. In 80% of the cases (n = 10), associated anomalies, including occlusions of the bronchus central to the mucocele, emphysematous changes of the peripheral lung fields, bronchogenic cyst, and anomalous branching of the bronchial tree and vascular structure were observed. CBA was detected in the right lobe in eight patients and the left lobe in the remaining four. No surgical intervention was performed in 5 CBA patients and the remaining 7 patients underwent surgery, including lobectomy in 5 patients and local resection in 2 patients. Among these 7 patients, 3 had a preoperative diagnosis of malignant disease, and the remaining 4 had severe clinical symptoms that could not be effectively treated by medicines. All patients were followed up, and none experienced obvious discomfort. CBA is a relatively rare and benign malformation disease. Chest CT is the procedure of choice for diagnosis. The presence of a bronchocele and surrounding emphysematous changes are typical radiologic findings in CBA. Surgery should be reserved only for patients with serious complications secondary to the atretic bronchus.</p>
url http://www.medsci.org/v09p0207.htm
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