| Literature DB >> 27891284 |
Malav Modi1, Amit Kumar Dey1, Ajay Mate1, Samir Rege1.
Abstract
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.Entities:
Year: 2016 PMID: 27891284 PMCID: PMC5116526 DOI: 10.1155/2016/2621383
Source DB: PubMed Journal: Case Rep Surg
Figure 1Chest X-ray showing an elevated right hemidiaphragm.
Figure 2Preoperative CT scan showing thickened small bowel loops in the right hemithorax with air specks in the bowel wall suggesting a strangulated diaphragmatic hernia.
Figure 3Intraoperative photo showing the inflammatory haemorrhagic fluid around the diaphragmatic defect.
Figure 4Intraoperative photo showing the right sided Morgagni's hernial defect.