Abdominal Catastrophe secondary to Paraduodenal Hernia

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چکیده

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Congenital left paraduodenal hernia causing chronic abdominal pain and abdominal catastrophe.

Paraduodenal hernias are the most common type of congenital internal hernia. Because of its overall rare incidence, this entity is often overlooked during initial assessment of the patient. Lack of specific diagnostic criteria also makes diagnosis exceedingly difficult, and the resulting diagnostic delays can lead to tragic outcomes for patients. Despite these perceived barriers to timely diagn...

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Intestinal obstruction secondary to left paraduodenal hernia

An internal hernia-congenital or acquired-is a protrusion of bowel through an opening in the peritoneum or mesentery. Internal hernias are the etiology of <2% of intestinal obstructions, with paraduodenal hernias being the most common type of congenital internal hernia. We report a case of a left paraduodenal hernia (LPDH) combined with partial small bowel obstruction in a 69-year-old male with...

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Right-sided paraduodenal hernia: rare cause of recurrent abdominal pain.

Right-sided paraduodenal hernia (PH) is a rare congenital malformation that arises due to a defect in the rotation of the middle intestine during embryogenesis. Though it is usually an incidental finding on autopsy or during laparotomy, it can be responsible for episodes of recurring abdominal pain or even acute abdomen (1,2). A search of the literature only revealed three cases of rightsided P...

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A Strangulated Paraduodenal Hernia

History.?On the 24th September, 1941, M., a Hindu male, aged 40, was admitted to hospital with a history of severe griping pain in the upper abdomen for two da3rs and inability to pass fseces or flatus for the last 12 hours. No history of previous illness. He had vomited twice during the last 3 hours, and had a feeling of nausea and severe thirst. Physical examination.?The patient was very rest...

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ژورنال

عنوان ژورنال: Indian Journal of Case Reports

سال: 2019

ISSN: 2454-129X,2454-1303

DOI: 10.32677/ijcr.2019.v05.i04.002