胸腔镜下肺叶切除术治疗婴幼儿右上支气管闭锁合并右下支气管奇型肺叶1例。

IF 0.9 Q4 ORTHOPEDICS
Nanako Nishida, Keisuke Yano, Yumiko Tabata, Chihiro Kedoin, Ayaka Nagano, Toshio Harumatsu, Yudai Tsuruno, Masakazu Murakami, Koshiro Sugita, Shun Onishi, Koji Yamada, Waka Yamada, Takafumi Kawano, Satoshi Ieiri
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引用次数: 0

摘要

支气管闭锁(BA)和奇叶(AL)是罕见的儿童先天性肺异常。我们在此报告一例胸腔镜手术治疗的婴儿BA合并AL。患者是一名8个月大的男孩,术前通过胎儿磁共振成像和产后增强计算机断层扫描诊断为右上叶BA (RUL)合并AL。采用吲哚菁绿(ICG)引导下的近红外荧光(NIRF)胸腔镜手术治疗RUL的BA。术中未发现上肺叶支气管,采用icg引导下的NIRF确认了RUL的肺血管。AL连接右下叶(RLL)。部分RLL,包括AL切除,在RUL切除后进行,以防止术后感染和扭转。术后过程平淡无奇。使用icg引导下的NIRF进行胸腔镜手术是一种罕见的婴儿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thoracoscopic Lobectomy for Right Upper Bronchial Atresia Combined With an Azygos Lobe of the Right Lower Lobe in an Infant Patient: A Case Report of a Rare Condition

Thoracoscopic Lobectomy for Right Upper Bronchial Atresia Combined With an Azygos Lobe of the Right Lower Lobe in an Infant Patient: A Case Report of a Rare Condition

Bronchial atresia (BA) and azygos lobe (AL) are rare congenital pulmonary abnormalities in pediatric patients. We herein report an infantile case of BA combined with AL that was treated with thoracoscopic surgery. The patient was an 8-month-old boy who was preoperatively diagnosed with BA of the right upper lobe (RUL) combined with an AL using fetal magnetic resonance imaging and postnatal enhanced computed tomography. Thoracoscopic surgery using indocyanine green (ICG)-guided near-infrared fluorescence (NIRF) was performed for BA of the RUL. In the operative findings, the upper lobe bronchus was not recognized, and the pulmonary vessels of the RUL were confirmed using ICG-guided NIRF. The AL was connected to the right lower lobe (RLL). Partial RLL, including AL resection, was performed after RUL resection to prevent postoperative infections and torsion. The postoperative course was uneventful. Thoracoscopic surgery using ICG-guided NIRF was safely performed in an infant with a rare condition.

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来源期刊
CiteScore
2.00
自引率
10.00%
发文量
129
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