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婴儿双侧先天性膈疝的延迟诊断:一例罕见病例报告。

Delayed Diagnosis of a Bilateral Congenital Diaphragmatic Hernia in an Infant: A Rare Case Presentation.

作者信息

Alameen Fatema, Almusalam Rashed, Alansari Meaad, Alshafei Abdulrahman

机构信息

Surgery, Bahrain Defence Force Royal Medical Services, Riffa, BHR.

Anaesthesia, Bahrain Defence Force Royal Medical Services, Riffa, BHR.

出版信息

Cureus. 2025 Jan 25;17(1):e77968. doi: 10.7759/cureus.77968. eCollection 2025 Jan.

Abstract

We report the case of a four-month-old male infant diagnosed incidentally with bilateral congenital diaphragmatic hernias. Our patient was found to have chest asymmetry during an unrelated hospital visit and bilateral diaphragmatic defects were confirmed on cross-sectional imaging. Surgical repair of a right-sided Bochdalek hernia and a left-sided Morgagni hernia was performed with excellent outcomes. This case report documents the rare occurrence of a bilateral late-presenting congenital diaphragmatic hernia, augments the limited existing knowledge, and highlights the variability in clinical outcomes. It provides valuable perspectives on the potentially improved survival rates in the uncommon manifestations of this condition.

摘要

我们报告了一例4个月大男婴偶然诊断为双侧先天性膈疝的病例。我们的患者在一次无关的医院就诊时被发现胸部不对称,横断面成像证实存在双侧膈肌缺损。对右侧Bochdalek疝和左侧Morgagni疝进行了手术修复,效果良好。本病例报告记录了双侧迟发性先天性膈疝的罕见情况,增加了现有的有限知识,并突出了临床结果的变异性。它为这种疾病罕见表现中潜在提高的生存率提供了有价值的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efb/11769598/9b35ff0b4bc2/cureus-0017-00000077968-i01.jpg

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