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先天性食管狭窄患儿的临床特征及治疗选择:单中心经验

Clinical profile and management options of children with congenital esophageal stenosis: A single center experience.

作者信息

Kurian Jujju Jacob, Jehangir Susan, Varghese Isaac Tharu, Thomas Reju Joseph, Mathai John, Karl Sampath

机构信息

Department of Paediatric Surgery, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

J Indian Assoc Pediatr Surg. 2016 Jul-Sep;21(3):106-9. doi: 10.4103/0971-9261.182581.

Abstract

AIM

The aim of the study is to review 7 patients with congenital esophageal stenosis treated in our institution from a diagnostic and therapeutic point of view.

MATERIALS AND METHODS

This is a retrospective cohort study of 7 patients treated in Christian Medical College, Vellore from 2008 to 2014. The data were analyzed with regards to age at onset of symptoms, investigative findings, age at definitive treatment, pathology, modalities of treatment, and outcomes.

RESULTS

Symptoms started within the 1(st) year of life in all children with a median age of 4 months. The time of delay in diagnosis ranged from 8 months to 81 months with a mean period of 37 months. About 6 patients had a lower esophageal stenosis and 1 patient had a mid-esophageal stenosis. About 4 of the 7 children underwent endoscopic balloon dilatation from elsewhere, with 2 of the above 4 undergoing a myotomy for a wrongly diagnosed achalasia. The number of dilatations ranged from 2 to 7 with a mean of 4 dilatations. Resection of the stenotic segment with end to end anastomosis was employed in 6 of the 7 patients, and a transverse colon interpositioning was done in 1 patient. An antireflux procedure was performed in one patient. Histopathological examination of the resected specimen revealed tracheobronchial remnant in 3 patients, fibromuscular thickening in 3 patients, and membranous web in 1 patient. Postoperatively, 2 of the 7 patients had asymptomatic gastroesophageal reflux and 1 patient had postoperative stricture requiring one session of endoscopic balloon dilatation. The mean follow-up period was 42 months (range 18-72 months). At the time of the last follow-up, all 7 patients were able to eat solid food, and none of the children were found to have symptoms suggestive of obstruction or gastroesophageal reflux. There was a statistically significant increase in the weight for age after the operation.

CONCLUSION

Congenital esophageal stenosis is rare and often confused with other causes of esophageal obstruction. Although endoscopic balloon dilatation offers an effective temporary relief, we feel that definitive surgery is curative. Long-term results following definitive surgery have been good, especially with respect to symptoms and weight gain.

摘要

目的

本研究旨在从诊断和治疗角度回顾我院收治的7例先天性食管狭窄患者。

材料与方法

这是一项对2008年至2014年在韦洛尔基督教医学院接受治疗的7例患者的回顾性队列研究。分析了症状出现时的年龄、检查结果、确定性治疗时的年龄、病理、治疗方式及预后等数据。

结果

所有儿童症状均在1岁内出现,中位年龄为4个月。诊断延迟时间为8个月至81个月,平均37个月。约6例患者为食管下段狭窄,1例为食管中段狭窄。7例儿童中约4例曾在其他地方接受内镜下球囊扩张,其中上述4例中的2例因误诊为贲门失弛缓症而接受了肌切开术。扩张次数为2至7次,平均4次。7例患者中有6例行狭窄段切除端端吻合术,1例行横结肠间置术。1例患者行抗反流手术。切除标本的组织病理学检查显示,3例为气管支气管残余,3例为纤维肌层增厚,1例为膜状蹼。术后,7例患者中有2例有无症状性胃食管反流,1例患者术后出现狭窄,需行一次内镜下球囊扩张。平均随访期为42个月(范围18 - 72个月)。在最后一次随访时,所有7例患者均能进食固体食物,且未发现儿童有提示梗阻或胃食管反流的症状。术后年龄别体重有统计学意义的增加。

结论

先天性食管狭窄罕见,常与其他食管梗阻原因混淆。虽然内镜下球囊扩张能提供有效的临时缓解,但我们认为确定性手术是治愈性的。确定性手术后的长期效果良好,尤其是在症状和体重增加方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee9f/4895732/9873901ce788/JIAPS-21-106-g001.jpg

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