ArticleCureus2025
A Rare Case of a Large Diaphragmatic Hernia With Upward Hepatic Transposition.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This study reports a rare case of an intrathoracic hepatic hernia identified during cadaveric dissection, characterized by a large congenital hiatus in the right diaphragmatic dome that permitted the herniation of the right hepatic lobe and displacement of adjacent abdominal viscera. The case was observed in the cadaver of an adult male, approximately 50 years old. During anatomical dissection, a defect measuring about 13 cm in the right dome of the diaphragm was found, resulting in the migration of the entire right hepatic lobe into the thoracic cavity, compression of the right lung, mediastinal shift, and displacement of other viscera, including splenic ectopia and migration of the hepatic flexure and transverse colon. The anatomical findings were documented photographically, measured, and analyzed in light of the existing literature. Intrathoracic liver hernias pose diagnostic challenges because they may mimic mediastinal or pulmonary masses. This case highlights the extensive thoracoabdominal reorganization that can result from congenital diaphragmatic defects and emphasizes the importance of thorough anatomical and imaging evaluations to ensure accurate diagnosis and to guide clinical and surgical management.
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