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Prolapsed sigmoid intussusception per anus in an elderly man: a case report
Penn S Teyha1, Alphonce Chandika, Vihar R Kotecha
1Department of Surgery, Weill Bugando University College of Health Sciences, P,O,Box 1464, Mwanza, Tanzania. viharkotecha@hotmail.com.
Insights
Adult intussusception is rare, often linked to underlying pathology. This case highlights an uncommon idiopathic presentation in a 66-year-old man, emphasizing the need for thorough investigation in adult intussusception.
Area of Science:
- Gastroenterology
- Surgical Case Reports
Background:
- Intussusception is well-documented in children but rare in adults (1-5% prevalence).
- Most adult intussusception cases involve an identifiable underlying pathology requiring investigation.
Purpose of the Study:
- To present a rare case of adult intussusception.
- To discuss the diagnostic and etiological considerations in adult intussusception.
Main Methods:
- Case report of a 66-year-old male presenting with anal mass and obstipation.
- Surgical intervention via laparotomy, sigmoid colectomy, and colostomy.
Main Results:
- Sigmoid colon intussusception into the rectum and anus identified during laparotomy.
- Histological findings revealed necrosis and chronic inflammation without an identifiable cause.
Conclusions:
- Adult intussusception typically has an identifiable cause (70-90%), unlike most pediatric cases.
- This case represents an uncommon idiopathic adult intussusception, lacking clear etiological factors despite examination and histology.
Background:
Intussusception in pediatrics is widely documented and well described. On the basis of the literature, however, adult intussusception is a rare entity with a prevalence of from 1% to 5%. The majority of adult patients with intussusception have an underlying pathology that needs to be identified by performing a proper physical examination and a wide array of investigations.
Case Presentation:
We present a case of a 66-year-old African man who presented to our emergency department with a mass protruding per anus with obstipation. During laparotomy, we found that the sigmoid colon had intussuscepted into the rectum and out from the anus. Other abdominal viscera were normal and without any obvious mesenteric lymphadenopathy. Sigmoid colectomy and spectacle colostomy were performed. Grossly, the excised bowel looked normal, but the histologic results showed features of necrosis and chronic inflammation.
Conclusion:
While 70% to 90% of cases of adult intussusception have an identifiable cause or lesion, most pediatric intussusceptions are idiopathic. The presentation in an adult described herein was of an uncommon idiopathic type with no identifiable cause found on the basis of the history, physical examination, or histological findings.
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