منابع مشابه
Congenital Strangulated Transmesenteric Hernia: A Rare Cause of Acute Bowel Obstruction
A case of congenital transmesenteric hernia leading to intestinal obstruction is being reported here.
متن کاملColopleural fistula due to strangulated Bochdalek hernia in an adult.
An elderly patient presented with a right sided pneumothorax due to strangulation of part of the colon through a congenital Bochdalek hernia. Congenital posterolateral diaphragmatic hernia of Bochdalek is rare in an adult and strangulation with pneumothorax has not been reported before.
متن کاملObturator hernia: a rare cause of acute small bowel obstruction
department, Tri-Service General Hospital, Taiwan, with diffuse abdominal pain for one day in April 2012. Her abdomen was distended, hypoactive and tender without palpable masses. Abdominal plain radiograph showed intestinal obstruction (Fig. 1). The computed tomography (CT) of abdomen demonstrated incarceration of the small bowel into the left obturator foramen (Fig. 2). An obturator hernia wit...
متن کاملAdult Bochdalek hernia with bowel incarceration.
Bochdalek hernias are rare in adults. We report 2 cases of Bochdalek hernia with bowel obstruction. The first case was a 74-year-old male patient who suffered from abdominal pain and chest tightness for 1 day. Chest radiography indicated a mass-like lesion above the left diaphragm. The pain could not be relieved by nasogastric tube decompression for 12 hours. We arranged computed tomography, wh...
متن کاملSpontaneous Transmesenteric Hernia: A Rare Cause of Small Bowel Obstruction in an Adult
The authors report a case of spontaneous transmesenteric hernia with strangulation in an adult. Transmesenteric hernia (TMH) is a rare cause of small bowel obstruction and is seldom diagnosed preoperatively, and most TMHs in adults are related to predisposing factors, such as previous surgery, abdominal trauma, and peritonitis. TMH are more likely to develop volvulus and strangulation or ischem...
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ژورنال
عنوان ژورنال: Surgical Research
سال: 2019
ISSN: 2689-1093
DOI: 10.33425/2689-1093.1009