同侧 Bochdalek 和 Morgagni 膈疝：病例报告。

Synchronous ipsilateral Bochdalek and Morgagni diaphragmatic hernias: a case report.

机构信息

University of California, San Francisco, CA 94143, USA.

出版信息

J Pediatr Surg. 2011 Dec;46(12):2383-6. doi: 10.1016/j.jpedsurg.2011.09.062.

DOI:10.1016/j.jpedsurg.2011.09.062

Abstract

The etiology of congenital diaphragmatic hernia (CDH) is unknown. Phenotypic patterns of CDH defects provide clues about normal diaphragm development and the pathophysiology of CDH. We report a case of a patient who was diagnosed with CDH postnatally and was found on imaging to have simultaneous Bochdalek and Morgagni hernias on the right side. During the operative repair of these defects, an additional left-sided Morgagni-type defect was also found. To the best of our knowledge, this form of CDH has not been previously reported.

摘要

先天性膈疝（CDH）的病因尚不清楚。CDH 缺陷的表型模式为正常膈肌发育和 CDH 的病理生理学提供了线索。我们报告了一例患者，该患者出生后被诊断为 CDH，并在影像学检查中发现右侧同时存在 Bochdalek 和 Morgagni 疝。在对这些缺陷进行手术修复时，还发现了左侧 Morgagni 型缺陷。据我们所知，这种形式的 CDH 以前尚未报道过。