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在一名患有复杂食管闭锁的婴儿中,使用球囊扩张术和胃肠造瘘管对十二指肠蹼进行创新性内镜治疗。

Innovative Endoscopic Management of a Duodenal Web Using Balloon Dilatation and a Gastrojejunal Tube in an Infant with Complex Esophageal Atresia.

作者信息

Kueppers Julia, Muensterer Oliver

机构信息

Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.

出版信息

J Laparoendosc Adv Surg Tech A. 2022 Dec;32(12):1269-1271. doi: 10.1089/lap.2022.0240. Epub 2022 Nov 23.

Abstract

Congenital partial duodenal obstruction (CPDO) is a rare type of intestinal obstruction, including webs and stenoses. Treatment has usually been operative by laparoscopy or laparotomy. Some have proposed endoscopic treatment due to a higher surgical risk in patients with CPDO. However, restenosis seems to be frequent after simple balloon dilatation. We report on a patient with CPDO and complex esophageal atresia in whom we used a gastrojejunal tube to keep the lumen open after endoscopic balloon dilatation over a guidewire. Follow-up endoscopy showed no evidence of restenosis. During the third endoscopy, the opening could be dilated to 15 mm without any complications and the gastrojejunal tube was removed. Since then, there were no clinical signs of obstruction, and no further endoscopic intervention was necessary. Using a gastrojejunal tube after endoscopic balloon dilatation of a duodenal web may lower the risk of restenosis. This technique should be considered in patients with comorbidities and considerable surgical risk that have a gastrostomy in place.

摘要

先天性十二指肠部分梗阻(CPDO)是一种罕见的肠梗阻类型,包括十二指肠蹼和狭窄。治疗通常通过腹腔镜手术或剖腹手术进行。由于CPDO患者手术风险较高,一些人提出了内镜治疗。然而,单纯球囊扩张术后再狭窄似乎很常见。我们报告了一例患有CPDO和复杂性食管闭锁的患者,在内镜下通过导丝进行球囊扩张后,我们使用了胃空肠管来保持管腔通畅。随访内镜检查未发现再狭窄迹象。在第三次内镜检查时,开口可扩张至15毫米,无任何并发症,胃空肠管被移除。从那时起,没有梗阻的临床症状,也无需进一步的内镜干预。在内镜下球囊扩张十二指肠蹼后使用胃空肠管可能会降低再狭窄的风险。对于合并其他疾病且手术风险较高且已行胃造口术的患者,应考虑采用这种技术。

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