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Intestinal obstruction in a patient with congenital transverse mesocolic defect with internal hernia: A case report
Samrat Shrestha1, Suresh Maharjan1, Bijay Raj Bhatta1
1National Academy of Medical Sciences, NAMS, Bir Hospital, Department of General Surgery, Kathmandu, Province-3, Nepal.
Insights
Congenital transverse mesocolic defects causing internal hernias are rare but serious. Prompt diagnosis and surgical repair are crucial for favorable outcomes in patients with unexplained bowel obstruction.
Area of Science:
- Gastroenterology
- Abdominal Surgery
- Radiology
Background:
- Internal hernias (IH) represent 5.8% of intestinal obstructions.
- Congenital transverse mesocolic defects are a rare cause of IH, posing diagnostic and surgical challenges.
Observation:
- A 71-year-old female with COPD presented with symptoms of acute intestinal obstruction.
- Contrast-enhanced computed tomography (CECT) identified a transition point, leading to exploratory laparotomy.
- A 7x6 cm defect in the transverse mesocolon was found, with ileal loops herniated into the lesser sac.
Findings:
- Surgical reduction of the herniated bowel and closure of the transverse mesocolic defect were performed.
- The patient recovered well postoperatively without complications.
Implications:
- Congenital transverse mesocolic internal hernias (TMIH) should be considered in atypical cases of unexplained bowel obstruction.
- Early diagnosis via imaging and timely surgical intervention are key to successful management of TMIH.
Introduction And Importance:
Internal hernias (IH) account for 5.8 % of all cases of intestinal obstruction. Intestinal obstruction due to congenital transverse mesocolic defects is a rare but significant clinical challenge that requires prompt recognition and surgical intervention.
Case Discussion:
A 71-year-old female with COPD presented with acute abdominal pain, abdominal distension, and vomiting. On physical examination, the abdomen was distended with generalized tenderness. Contrast-enhanced computed tomography (CECT) revealed a transition point at the ileum. Failure of conservative management led to exploratory laparotomy that revealed a 7 cm ∗ 6 cm defect in the transverse mesocolon with herniation of ileal loops into the lesser sac. The hernia was reduced, and the defect closed. Postoperatively, the patient recovered well without complications.
Clinical Discussion:
IH, including transverse mesocolic IH (TMIH), are often asymptomatic or present with vague abdominal pain. They are challenging to diagnose clinically and radiologically. It has been reported in several studies, with internal hernias due to mesocolic defects accounting for about 0.2-0.9 % of all abdominal hernias. CECT offers a diagnostic accuracy of 77 %. Surgical intervention is necessary for complicated cases, with a focus on reducing the herniated bowel and closing the defect. This case highlights the importance of considering congenital mesocolic defects in the differential diagnosis of unexplained intestinal obstruction, particularly in elderly patients.
Conclusion:
Congenital TMIH should be considered in the differential diagnosis of patients with unexplained bowel obstruction, especially when the clinical picture is atypical. Early diagnosis with imaging and surgical repair leads to favorable outcomes, as demonstrated in this case.
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