Diagnosing Congenital Diaphragmatic Eventration Presenting With Transient Cardiac Dextroposition in an Adult: A Case Report and Literature Review.

Q4 Medicine
Case Reports in Pulmonology Pub Date : 2026-08-05 eCollection Date: 2026-01-01 DOI:10.1155/crpu/1851328
Yeganeh Rafiei, Behnaz Movahedi, Fatemeh Bayat, Fatemeh Zohrian
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引用次数: 0

Abstract

Congenital diaphragmatic eventration (CDE) is a rare developmental anomaly characterized by abnormal elevation of an intact hemidiaphragm due to deficient muscular development. Although often asymptomatic in adults, it may present with respiratory or gastrointestinal complaints. We report a 65-year-old man with congenital left hemidiaphragmatic eventration associated with gastric displacement and colonic interposition. He initially presented with chest pain and was found to have cardiac dextroposition. Multimodality imaging, including fluoroscopy, demonstrated a transient rightward cardiac displacement that became more apparent after postprandial gastric distention and regressed as gastric decompression occurred. This dynamic finding suggests that gastrointestinal distention and associated mass effect can exacerbate mediastinal displacement in patients with CDE. This case highlights the importance of considering congenital diaphragmatic anomalies in adults with atypical chest symptoms and emphasizes the value of dynamic imaging in clarifying reversible cardiac displacement.

诊断成人先天性膈肌膨出伴一过性心脏右移一例报告及文献复习。
先天性膈肌膨出(CDE)是一种罕见的发育异常,其特征是由于肌肉发育不足而导致完整的半膈异常升高。虽然成人通常无症状,但可能出现呼吸或胃肠道不适。我们报告一个65岁的男性先天性左半膈突出与胃移位和结肠间置。患者最初表现为胸痛,发现心脏右移。包括透视在内的多模态成像显示一过性右心移位,在餐后胃扩张后变得更加明显,并在胃减压后消退。这一动态发现表明,胃肠道膨胀和相关的肿块效应可加剧CDE患者的纵隔移位。本病例强调了在不典型胸部症状的成人中考虑先天性膈异常的重要性,并强调了动态成像在澄清可逆性心脏移位中的价值。
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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来源期刊
Case Reports in Pulmonology
Case Reports in Pulmonology Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.80
自引率
0.00%
发文量
23
审稿时长
13 weeks
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