A Rare Diaphragmatic Hernia in Adults: Larrey’s Hernia
Congenital diaphragmatic hernia is a rare condition characterised by an embryonic defect in the diaphragmatic dome, causing the abdominal viscera to ascend into the thorax. Larrey’s diaphragmatic hernia is a rare condition, mainly diagnosed in the prenatal and neonatal periods. Its diagnosis in adults is exceptional. There are few cases reported in the literature in adults. Its symptoms are non-specific. We report a case of Larrey’s hernia in a 72-year-old patient revealed by digestive symptoms, and through a review of the literature, we highlight data on the diagnosis, surgical treatment and prognosis of this condition.
Authors
- R Lebeau (ORCID: https://orcid.org/0000-0003-4345-2800)
- Blaise Amos Kouakou
- Kouamé Bernadin Kouakou
- Ahou Bernadette N’Dri
- Kouakou Ibrahim Anzoua
- Mamadou Traoré (ORCID: https://orcid.org/0000-0003-0558-1724)
- Inza Bamba
- Bamourou Diané (ORCID: https://orcid.org/0000-0001-9940-4790)
- Kalou Ismaël Leh Bi
- Serges Amos Ekra
- Djahou Ezeckiel Akowendo
Institutions
- Hôpital Boucicaut (FR)
Publication Details
- Journal
- Surgical Science
- Published
- 2025-01-01
- DOI
- https://doi.org/10.4236/ss.2025.169041
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00