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Updated: Jun 7, 2026

Multimodality Diagnosis of Mesenteric Ischemia
Published on: July 21, 2023
Infarction of a polyp within a mesenteric cyst: An unusual presentation as an acute abdomen
Sonia Gon1, Bipasa Majumdar, Aditi Bhattacharyya
1Department of Pathology, R G Kar Medical College & Hospital, Kolkata, India.
Insights
A rare case of a mesenteric cyst complicated by an infarcted polyp, leading to acute abdomen in a child, is presented. This unique presentation has not been previously documented in medical literature.
Area of Science:
- Pediatric Surgery
- Gastrointestinal Pathology
- Abdominal Imaging
Background:
- Mesenteric cysts are rare congenital anomalies, typically presenting as asymptomatic abdominal masses.
- Complications such as infection, torsion, or rupture are uncommon but can lead to acute surgical emergencies.
- Polypoid lesions within mesenteric cysts are exceptionally rare, with infarction being an even rarer sequela.
Observation:
- A five-year-old male child presented with symptoms indicative of acute abdomen.
- Diagnostic imaging revealed a mesenteric cyst.
- A polypoid structure within the cyst was identified as infarcted.
Findings:
- The patient's acute abdomen was attributed to an infarcted polyp within a mesenteric cyst.
- This specific complication, polyp infarction within a mesenteric cyst, represents a novel finding in the existing medical literature.
- Histopathological examination confirmed the presence of infarction within the polyp.
Implications:
- This case expands the spectrum of potential complications associated with mesenteric cysts in pediatric patients.
- It highlights the importance of considering unusual etiologies for acute abdomen in children.
- Further investigation into the pathogenesis of polyp formation and infarction within mesenteric cysts may be warranted.
Abstract:
A case of mesenteric cyst in a five-year-old male child who presented with acute abdomen due to an infarcted polyp present within the cyst is reported. To the best of our knowledge, such an event has never been reported in the literature previously.
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