Case Report: Marfan syndrome complicated with obturator hernia.

Abstract

<h4>Background</h4>Obturator hernia is an extremely rare subtype of abdominal wall hernia, typically occurring in elderly female with a history of chronic increased intra-abdominal pressure or multiple pregnancies. However, it is rarely encountered in young individuals, which may lead to diagnostic oversight. Here, we report a case of a young female with Marfan syndrome who developed a left obturator hernia.<h4>Patient presentation</h4>A young female with Marfan syndrome and pectus excavatum presented with 6 h of persistent severe left inguinal pain.<h4>Diagnostic process</h4>Physical examination revealed a 2 cm × 2 cm localized swelling in the upper medial aspect of the left thigh, medial to the inguinal ligament. Left Howship-Romberg sign (+). Computed tomography (CT) examination indicated pectus excavatum, cardiomegaly, and a left obturator hernia.<h4>Intervention</h4>Based on these findings, laparoscopic preperitoneal inguinal hernia mesh repair was performed.<h4>Outcome</h4>The patient was discharged on postoperative day 3 and followed up for 14 months. Recovery was uneventful with no complications.<h4>Conclusion</h4>This case highlights the importance of differential diagnostic thinking for hernias in patients with connective tissue diseases.