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Pediatric gastric mesothelial cyst presenting with abdominal distention and pain: A case report
Ehsanullah Rasouli1, Abdullah Wahdat1, Ali Rahimi2
1Aria Apollo Hospital, Herat, Afghanistan.
Insights
Pediatric gastric mesothelial cysts are rare and can mimic other abdominal masses. Histopathological confirmation is crucial for accurate diagnosis and management of these rare gastric cysts.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Pathology
Background:
- Mesothelial gastric cysts are exceptionally rare in children, often presenting diagnostic challenges.
- These cysts can be mistaken for more common pediatric abdominal masses like mesenteric or duplication cysts.
Observation:
- A 3-year-old boy presented with a 6-month history of abdominal distention and pain.
- Imaging revealed a large cystic mass, initially presumed to be mesenteric.
- Intraoperative findings confirmed the cyst's origin from the gastric wall.
Findings:
- Histopathological examination definitively diagnosed a mesothelial cyst.
- The cyst was unilocular, lined by mesothelial cells, and lacked atypia or mitoses.
- Complete surgical excision was performed.
Implications:
- This case highlights the importance of considering rare gastric pathologies in pediatric abdominal masses.
- Accurate diagnosis relies heavily on histopathological analysis.
- Surgical excision is the definitive treatment for gastric mesothelial cysts, with favorable outcomes and no reported recurrence at 6 months.
Introduction:
Mesothelial gastric cysts are exceedingly rare in pediatric patients, often mimicking mesenteric or duplication cysts. This case highlights diagnostic challenges and underscores the importance of histopathological confirmation.
Presentation Of Case:
A 3-year-old boy presented with 6 months of progressive abdominal distention and intermittent pain. Imaging revealed a 12 × 10 cm unilocular cystic mass, initially suspected to be mesenteric. Intraoperatively, the cyst originated from the gastric wall. Complete excision and histopathology confirmed a mesothelial cyst. Histopathology showed a unilocular cyst lined by flattened mesothelial cells resting on a fibro-collagenous wall, without atypia or mitoses.
Discussion:
Gastric mesothelial cysts are rarely reported in children. Surgical excision remains definitive, with no recurrence at 6-month follow-up.
Conclusion:
This case emphasizes the need to consider rare gastric cysts in pediatric abdominal masses and the role of histopathology in diagnosis.
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