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Case Report

[English]
Unusual Giant Arteriovenous Malformation in Jejunum: A Case Report
DongJa Kim, JaIl Goo
J Korean Assoc Pediatr Surg 2017;23(2):52-54.   Published online December 20, 2017
DOI: https://doi.org/10.13029/jkaps.2017.23.2.52

Polypoid or tumorous arteriovenous malformation (AVM) of small intestine is rare and can be misdiagnosed as other tumorous conditions. We experienced a rare case of giant jejunal AVM in a 15-year-old boy, who complained of intense abdominal pain. Ultrasonography and contrast-enhanced CT revealed a 13.5-cm-sized multiseptated cystic mass arising in small intestine, which was mimicking submucosal tumor. It was successfully treated by surgical resection. The specimen showed a multilobulated outbulging submucosal mass in jejunum. Histopathologic evalulation confirmed AVM located in the submucosa, muscularis propria and subserosa. This case is the largest AVM of small intestine among which has ever been reported.

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Original Article

[English]
Gastroduodenal Intussusception due to Gastric Submucosal Hemangiomatosis
Soo Jin Na Choi, Sang Young Chung, Shin Kon Kim, Sang Woo Jung
J Korean Assoc Pediatr Surg 2000;6(2):149-152.   Published online December 31, 2000
DOI: https://doi.org/10.13029/jkaps.2000.6.2.149

Gastroduodenal intussusception, an invagination of a part of the gastric wall through the pyloric canal into the duodenum is a rare condition. Gastroduodenal intussusception is caused by a mobile usually benign gastric tumor. However, gastroduodenal intussusception by gastric submucosal hemangiomatosis is not documented. We have managed a case of gastric submucosal tumor leading to gastroduodenal intussusception in 2 years and 10 months old boy. The tumor was 10 × 5 × 3 cm in size in posterior wall of gastric antrum. Laparotomy, manual reduction of the intussusception, and wedge resection of posterior gastric wall including the tumor were performed. Pathologic diagnosis was a submucosal hemangiomatosis.

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