A Rare Case of a Large Diaphragmatic Hernia With Upward Hepatic Transposition

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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Publication Details

Journal
Cureus
Published
2025-12-24
DOI
https://doi.org/10.7759/cureus.100034
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
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article

A Rare Case of a Large Diaphragmatic Hernia With Upward Hepatic Transposition

José Aderval Aragão, André Henrique V de Almeida, Leonardo F Mello, Danila F Silva et al.
Cureus
Congenital Diaphragmatic Hernia Studies
article

A Rare Case of a Large Diaphragmatic Hernia With Upward Hepatic Transposition

José Aderval Aragão, André Henrique V de Almeida, Leonardo F Mello, Danila F Silva, Roberto F de Oliveira, Ariana Albertina A Leal, Bento João Abreu
article en

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.

CureusVol. 17(12)
Universidade Federal de Sergipe (BR), Universidade Estadual de Feira de Santana (BR), Universidade Federal do Rio Grande do Norte (BR), Universidade Tiradentes (BR), Varian Medical Systems (United States) (US)
Openalex Percentile: Top 26%
Congenital Diaphragmatic Hernia Studies
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