Diaphragmatic morgagni in adult: a case report

A 70-year-old male patient with a history of systemic hypertension, gouty arthritis, and possible chronic kidney disease presented with right flank pain, nausea, and decreased appetite. Examinations revealed a right-sided incarcerated diaphragmatic hernia in the anterior region, with protrusion of adipose tissue and loops of small intestine. A laparoscopic surgery was performed, during which the herniated contents were reduced, and a hernia defect approximately 4 cm in size was found and repaired. Post-surgery, he developed complications including pulmonary thromboembolism, intestinal perforation, and fistula, which required reoperation, and progressive clinical deterioration, ultimately leading to death. This case report presents a rare instance of congenital hernia diagnosed through imaging after the onset of nonspecific clinical symptoms. It emphasizes the importance of considering this pathology among differential diagnoses of acute abdomen for prompt diagnosis and appropriate management through surgical intervention.

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Publication Details

Journal
International Surgery Journal
Published
2024-11-27
DOI
https://doi.org/10.18203/2349-2902.isj20243554
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
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article

Diaphragmatic morgagni in adult: a case report

Fernanda Bombonato Smecellato, Eloísa Ianes Frota, Marcelo Queiroz Oliveira, Rodolfo Correa et al.
International Surgery Journal
Congenital Diaphragmatic Hernia Studies
article

Diaphragmatic morgagni in adult: a case report

Fernanda Bombonato Smecellato, Eloísa Ianes Frota, Marcelo Queiroz Oliveira, Rodolfo Correa, Larissa Silva Sande, Letícia Vieira Guerrer, Sérgio Luis Aparecido Brienze
article en

Abstract

A 70-year-old male patient with a history of systemic hypertension, gouty arthritis, and possible chronic kidney disease presented with right flank pain, nausea, and decreased appetite. Examinations revealed a right-sided incarcerated diaphragmatic hernia in the anterior region, with protrusion of adipose tissue and loops of small intestine. A laparoscopic surgery was performed, during which the herniated contents were reduced, and a hernia defect approximately 4 cm in size was found and repaired. Post-surgery, he developed complications including pulmonary thromboembolism, intestinal perforation, and fistula, which required reoperation, and progressive clinical deterioration, ultimately leading to death. This case report presents a rare instance of congenital hernia diagnosed through imaging after the onset of nonspecific clinical symptoms. It emphasizes the importance of considering this pathology among differential diagnoses of acute abdomen for prompt diagnosis and appropriate management through surgical intervention.

International Surgery JournalVol. 11(12)
Faculdade de Medicina de São José do Rio Preto (BR), Hospital de Base (BR)
Good health and well-being
Openalex Percentile: Top 59%
Congenital Diaphragmatic Hernia Studies
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