Jie Zhang, Song Sun, Shan Zheng, Yang-Yang Ma, Gong Chen
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The cystic wall was composed of smooth muscles lined with the gastric mucosal epithelium and a small amount of intestinal epithelium. Scattered glandular epithelium and a small amount of pancreatic tissue were observed in smooth muscle. Immunohistochemistry revealed positivity for gastrin, insulin, and smooth muscle actin, confirming the diagnosis of GA. In addition, the Ki-67 proliferation index was low.</p><p><strong>Conclusion: </strong>We report a case of GA in children, successfully treated with laparoscopic surgery. Ultrasound and computed tomography may be helpful in differential diagnosis when detecting low-density septal lesions biased toward one side. 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引用次数: 0
摘要
背景:儿童胃腺肌瘤(GA)是一种相对罕见的疾病,目前关于其最佳诊断方法和治疗策略的知识有限。为了提高我们对GA特别是儿童的理解,我们报告了一例4个月大的男孩,并对现有文献进行了全面的回顾。病例总结:一名4个月大的男婴因胃内容物反复呕吐2个月入院。超声检查显示幽门管肌厚3.2 mm,直径14.6 mm,长17.6 mm。病理发现:肿块大小约2.8 cm × 2 cm × 1.5 cm,颜色灰白色。囊壁由平滑肌组成,内衬胃粘膜上皮和少量肠上皮。平滑肌内可见散在腺上皮和少量胰腺组织。免疫组化显示胃泌素、胰岛素、平滑肌肌动蛋白阳性,证实GA的诊断。此外,Ki-67增殖指数较低。结论:我们报告了一例儿童GA,成功地通过腹腔镜手术治疗。超声和计算机断层扫描可能有助于鉴别诊断时,发现低密度的中隔病变偏向一侧。我们还回顾了关于儿童GA的现有文献数据。
Background: Gastric adenomyoma (GA) in children is a relatively rare condition, and currently, there is limited knowledge regarding its optimal diagnostic methods and treatment strategies. To improve our understanding GA particularly in children, one case of a 4-month-old boy was reported and existing literature was comprehensively reviewed.
Case summary: A 4-month-old boy was admitted to the hospital with a 2-month history of recurrent vomiting of gastric contents. Ultrasound examination demonstrated that the pyloric canal muscle was 3.2 mm in thickness, 14.6 mm in diameter, and 17.6 mm in length. Pathological finding showed that a mass approximately 2.8 cm × 2 cm × 1.5 cm in size and grayish-white in color was detected. The cystic wall was composed of smooth muscles lined with the gastric mucosal epithelium and a small amount of intestinal epithelium. Scattered glandular epithelium and a small amount of pancreatic tissue were observed in smooth muscle. Immunohistochemistry revealed positivity for gastrin, insulin, and smooth muscle actin, confirming the diagnosis of GA. In addition, the Ki-67 proliferation index was low.
Conclusion: We report a case of GA in children, successfully treated with laparoscopic surgery. Ultrasound and computed tomography may be helpful in differential diagnosis when detecting low-density septal lesions biased toward one side. We also review the existing literature data regarding GA in children.