婴儿双侧先天性膈疝的延迟诊断:一个罕见的病例

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2025-01-25 eCollection Date: 2025-01-01 DOI:10.7759/cureus.77968
Fatema Alameen, Rashed Almusalam, Meaad Alansari, Abdulrahman Alshafei
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引用次数: 0

摘要

我们报告的情况下,四个月大的男婴诊断偶然与双侧先天性膈疝。我们的病人在一次不相关的医院就诊中发现胸部不对称,横断面成像证实了双侧膈肌缺陷。手术修复右侧Bochdalek疝和左侧Morgagni疝的效果很好。本病例报告记录了罕见的双侧迟发先天性膈疝,增加了有限的现有知识,并强调了临床结果的可变性。它提供了有价值的观点,对潜在的提高生存率在这种情况的不常见的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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.

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