交通性支气管肺前肠畸形IB型:诊断和手术挑战。

Pub Date : 2021-12-13 eCollection Date: 2021-01-01 DOI:10.1055/s-0041-1740321
Bhushanrao Jadhav, Ranjithatharsini Vaseeharan, Prabhu Sekaran, Semiu Eniola Folaranmi, Karim Awad
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引用次数: 3

摘要

沟通性支气管肺前肠畸形(CBPFM)极为罕见。我们报告了一个复杂的IB型CBPFM病例,伴有食管闭锁和远端气管食管瘘(EA/TOF),十二指肠闭锁/环状胰腺(DA/AP)和肠道旋转不良,并在第3天接受了EA/TOF的初步修复。第8天的胆汁抽吸提示上消化道(GI)造影显示十二指肠梗阻,右肺下叶与食管之间的交通(T8-T9水平)。DA/AP和旋转不良通过胃空肠吻合术和Ladd手术修复。重复对比吞咽检查发现从食道到右下叶(T5-T6水平)的第二次交通,提高了对复发性TOF的怀疑。胸部计算机断层扫描(CT)证实上述发现,右肺血供异常。探索性开胸术发现一个三叶肺。然而,下叶扩大,并在两个不同的位置连接到食道。患儿在切断食管连接和部分右下肺叶切除术后康复。CBPFM是一种非常罕见的异常,需要高度怀疑,使用上消化道造影系列和CT扫描进行诊断。治疗的选择是切除患肺和切断食道交通。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Communicating Bronchopulmonary Foregut Malformation Type IB: Diagnostic and Surgical Challenges.

Communicating Bronchopulmonary Foregut Malformation Type IB: Diagnostic and Surgical Challenges.

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Communicating Bronchopulmonary Foregut Malformation Type IB: Diagnostic and Surgical Challenges.

Communicating bronchopulmonary foregut malformations (CBPFM) are extremely rare. We present a complex case of type IB CBPFM with esophageal atresia and distal tracheoesophageal fistula (EA/TOF), duodenal atresia/annular pancreas (DA/AP), and intestinal malrotation who underwent primary repair for EA/TOF on day 3. Bilious aspirates on day 8 prompted an upper gastrointestinal (GI) contrast revealing a duodenal obstruction and communication between the right lung lower lobe and the esophagus (T8-T9 level). DA/AP and malrotation were repaired by a gastrojejunostomy and Ladd's procedure. A repeat contrast swallow identified a 2nd communication from the esophagus into the right lower lobe (T5-T6 level) raising the suspicion of a recurrent TOF. Computed tomography (CT) thorax confirmed above findings with an anomalous blood supply to right lung. An exploratory thoracotomy identified a three-lobed lung. However, the lower lobe was enlarged and connected in two separate locations to the esophagus. The child recovered after the disconnection of the esophageal connections and partial right lower lobectomy. CBPFM are extremely rare anomalies requiring a high index of suspicion, use of an upper GI contrast series, and CT scans for diagnosis. The treatment of choice is resection of the affected lung and disconnection of the esophageal communications.

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