{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,11]],"date-time":"2026-02-11T14:41:13Z","timestamp":1770820873185,"version":"3.50.1"},"reference-count":12,"publisher":"Wiley","license":[{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Surgery"],"published-print":{"date-parts":[[2016]]},"abstract":"<jats:p>Morgagni hernia is a rare type of congenital diaphragmatic hernia. It accounts for only 3% of all diaphragmatic hernias. The defect is small and hernia being asymptomatic in the majority presents late in adulthood. Obstruction or incarceration in Morgagni hernia is uncommon. We report a rare occurrence of strangulated Morgagni hernia. A 40-year-old gentleman presented to our emergency department with features of intestinal obstruction. Computed tomography of the chest and abdomen showed a strangulated right Morgagni hernia. An exploratory laparotomy was performed with resection of the ischemic bowel segment with anastomosis and a primary repair of the diaphragmatic defect. Postoperative recovery was uneventful and asymptomatic at follow-up.<\/jats:p>","DOI":"10.1155\/2016\/2621383","type":"journal-article","created":{"date-parts":[[2016,11,7]],"date-time":"2016-11-07T21:08:48Z","timestamp":1478552928000},"page":"1-3","source":"Crossref","is-referenced-by-count":8,"title":["Strangulated Morgagni\u2019s Hernia: A Rare Diagnosis and Management"],"prefix":"10.1155","volume":"2016","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0824-5577","authenticated-orcid":true,"given":"Malav","family":"Modi","sequence":"first","affiliation":[{"name":"Department of Surgery, Seth G.S. 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