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Published on: February 19, 2022
Gastric Duplication Cyst Presenting as Massive Gastrointestinal Bleeding
Alexey Youssef1,2, Alexander Ibrahim1, Zuheir AlShehabi3,4
1Faculty of Medicine, Tishreen University, Latakia, Syria.
Insights
Gastric duplication cysts (GDCs) are rare congenital anomalies. This case highlights a GDC presenting as massive gastrointestinal bleeding in an infant, successfully treated with surgery.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Congenital Anomalies
Background:
- Gastric duplication cysts (GDCs) are uncommon congenital malformations.
- GDCs can manifest with diverse clinical presentations, ranging from asymptomatic masses to severe gastrointestinal (GI) bleeding.
Observation:
- A 10-month-old infant presented with massive GI hemorrhage and hematemesis.
- Initial abdominal ultrasound was inconclusive; computerized tomography (CT) was initially unavailable.
- Repeated esophagogastroduodenoscopies revealed GDC penetration into the gastric lumen.
Findings:
- Computerized tomography later confirmed the GDC's intraluminal extension.
- The infant experienced massive GI bleeding attributed to the GDC.
Implications:
- This case underscores the importance of considering GDCs in infants with unexplained GI hemorrhage.
- Diagnostic challenges highlight the utility of endoscopy in GDC evaluation.
- Surgical resection remains an effective treatment for symptomatic GDCs.
Abstract:
Gastric duplication cysts (GDCs) are rare congenital anomalies. Presentation of GDCs varies from an asymptomatic abdominal mass to fulminant or massive gastrointestinal (GI) bleeding. Herein, we describe a case of a GDC in a 10-month-old infant presenting with unexplained massive GI hemorrhage and hematemesis. An abdominal ultrasound was negative, while computerized tomography was, initially, inaccessible. Through a series of repeated esophagogastroduodenoscopies, we documented penetration of the GDC into the gastric cavity that was later confirmed by computerized tomography. The patient was treated successfully with surgical resection.
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