Nagaya M, Kato J, Niimi N, Tanaka S, Akiyoshi K, Tanaka T
Department of Pediatric Surgery, Central Hospital, Aichi Prefectural Colony, Kasugai, Japan.
J Pediatr Surg. 1998 Apr;33(4):653-4. doi: 10.1016/s0022-3468(98)90338-4.
This is a report of an extremely rare case of isolated cavernous hemangioma of the stomach found in a neonate. Hematemesis developed in a 7-day-old baby boy weighing 2.8 kg at birth. This was followed by melena. Endoscopic examination findings showed a large hemorrhagic mass on the lesser curvature of the stomach. During laparotomy, a large vascular tumor was identified and subtotal gastrectomy was carried out. On section, the tumor extended through the submucosa to the serosal surface. Histological diagnosis was cavernous hemangioma. The authors could collect only 10 cases of hemangioma of the stomach diagnosed in childhood from the world literature.
本文报告了一例极为罕见的新生儿孤立性胃海绵状血管瘤病例。一名出生时体重2.8千克的7日龄男婴出现了呕血症状，随后出现黑便。内镜检查发现胃小弯处有一个大的出血性肿物。剖腹手术中，发现一个大的血管性肿瘤并进行了胃次全切除术。切片显示肿瘤从黏膜下层延伸至浆膜表面。组织学诊断为海绵状血管瘤。作者仅从世界文献中收集到10例儿童期诊断的胃血管瘤病例。
