Single-stage bilateral lobectomy for bilateral congenital lobar emphysema: A case report

Nardos Mulu Admasu , Woubedel Kiflu Aklilu , Yirgalem Teklebirhan Gebreziher , Samuel Sisay
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Abstract

Introduction

Congenital lobar emphysema (CLE) is a condition characterized by overinflation of one or more pulmonary lobes due to air-trapping, which can cause severe compression of adjacent structures. Bilateral CLE is rare but can cause severe respiratory distress.

Case presentation

A 9-day-old female born at 38 weeks who had respiratory distress since birth was transferred to our institution for further care. The prenatal history was unremarkable. Bloodwork was within normal limits.

She was put on non-invasive continuous positive airway pressure. On physical exam she had decreased air entry over the lower two-thirds of the lung fields bilaterally. A chest x-ray revealed air trapping in the left upper hemithorax and the right lower hemithorax. Contrast-enhanced computed tomography confirmed bilateral CLE of the left upper lobe and the right middle lobe causing severe compression of the adjacent lobes. She was intubated and transferred to the intensive care unit. Due to concerns regarding adherence to follow up and further access to medical care, we decided to attempt a single-stage bilateral thoracotomy/lobectomy. On day of life 15 she was taken to the operating room. We first did a left thoracotomy and a left upper lobectomy. The operation was uneventful, and she remained hemodynamically stable throughout the case. We closed the left thoracotomy and decided to proceed with a right thoracotomy and right middle lobectomy. She tolerated that procedure well. She was extubated in the operating room and was transferred to the intensive care unit. She recovered well and was discharged from the hospital on no respiratory support on postoperative day 13. Six months after the operation she remains asymptomatic and is thriving well.

Conclusion

In a resource-limited setting with poor parental adherence for follow-up, single-stage bilateral thoracotomy is a viable option for the management of bilateral congenital lobar emphysema.

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单阶段双侧肺叶切除术治疗双侧先天性肺叶气肿:病例报告
导言先天性肺叶气肿(Congenital lobar emphysema,CLE)是一种由于空气潴留导致一个或多个肺叶过度膨胀的疾病,可对邻近结构造成严重压迫。双侧 CLE 很少见,但可导致严重的呼吸窘迫。病例介绍 一名出生 9 天、孕 38 周的女婴,出生后即出现呼吸窘迫,转入我院接受进一步治疗。产前病史无异常。她接受了无创持续气道正压治疗。体格检查时,她双侧肺野下三分之二的进气量减少。胸部 X 光片显示左上胸腔和右下胸腔有空气潴留。对比增强计算机断层扫描证实,左上叶和右中叶的双侧CLE导致邻近肺叶严重受压。她被插管并转入重症监护室。由于担心随访和进一步就医,我们决定尝试单阶段双侧胸腔/肺叶切除术。在生命的第 15 天,她被送进了手术室。我们首先进行了左侧胸廓切开术和左上肺叶切除术。手术很顺利,她在整个手术过程中血流动力学保持稳定。我们关闭了左侧胸腔切口,决定继续进行右侧胸腔切口和右侧中叶切除术。她对手术耐受良好。她在手术室拔管后被转入重症监护室。她恢复良好,术后第 13 天出院时已无需呼吸支持。结论 在资源有限且家长不重视随访的情况下,单段双侧开胸手术是治疗双侧先天性肺叶气肿的可行方案。
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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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