首页> 外文期刊>International surgery >Success of Minimally Invasive Transumbilical Single-Incision Laparoscopic Surgery (T-SILS) Plus Double-Balloon Endoscopy (DBE) for Pediatric Intestinal Angiodysplasia: A Case Report
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Success of Minimally Invasive Transumbilical Single-Incision Laparoscopic Surgery (T-SILS) Plus Double-Balloon Endoscopy (DBE) for Pediatric Intestinal Angiodysplasia: A Case Report

机译:微创经脐单切口腹腔镜手术(T-SILS)加双气囊内窥镜检查(DBE)治疗小儿肠血管发育不良的成功案例:病例报告

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We describe here a child with angiodysplasia of the small intestine, diagnosed by double-balloon endoscopy (DBE), who was treated with transumbilical single-incision laparoscopic surgery (T-SILS). A 9-year-old boy presented to another hospital with intermittent fresh melena of a duration of 5 months and 4 days. Anoscopy and gastric mucosal membrane scintigraphy were unsuccessful diagnostically, and he was referred to our hospital for further examination and treatment. Under general anesthesia, we performed DBE by an anal route, with the ileum assessed for a distance of about 150 cm from the ileocecal valve. Although no bleeding lesion was found in the colon, a flat elevated venous lake approximately 20 mm in size was observed 20 cm from the ileocecal valve, suggesting angiodysplasia of the small intestine. A tattoo was made under DBE, and wedge resection by T-SILS was performed 1 month later under general anesthesia. The excised specimen appeared as a flat, elevated venous lake approximately 20 mm in size. Histopathologic analysis revealed several dilated and distorted veins within the submucosa of the small intestine. The patient was diagnosed with angiodysplasia of the small intestine. His postoperative course was uneventful, and he remained free of recurrent gastrointestinal bleeding 18 months after the operation. This is the first case report showing the diagnosis, localization, and tattooing of an obscure gastrointestinal bleeding lesion of the small intestine by preoperative DBE and removal of the lesion by subsequent T-SILS in children.
机译:我们在这里描述了一个小肠血管增生的孩子,该孩子经双气囊内窥镜检查(DBE)诊断,并接受了脐带单切口腹腔镜手术(T-SILS)治疗。一名9岁男孩因间歇性新鲜黑斑病出现在另一家医院,病程为5个月零4天。肛门镜检查和胃粘膜闪烁闪烁成像检查未成功诊断,他被转介到我院进一步检查和治疗。在全身麻醉下,我们通过肛门途径进行DBE,并评估回肠距回盲瓣约150 cm的距离。尽管在结肠中未发现出血灶,但在距回盲瓣约20 cm处观察到一个扁平的高位静脉湖,大小约为20 mm,表明小肠血管增生。在DBE下进行纹身,并在全身麻醉下1个月后通过T-SILS进行楔形切除。切除的标本显示为大小约20毫米的平坦的高架静脉湖。组织病理学分析显示小肠粘膜下层内有数个扩张和扭曲的静脉。患者被诊断出小肠血管增生异常。术后过程平稳,术后18个月无胃肠道出血。这是第一例病例报告,显示了术前DBE对小肠隐蔽性胃肠道出血病变的诊断,定位和纹身,并在随后的儿童中通过T-SILS去除了病变。

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