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短肠综合征中的吻合口溃疡:多学科方法的新建议

Anastomotic ulcers in short bowel syndrome: New suggestions from a multidisciplinary approach.

作者信息

Fusaro Fabio, Tambucci Renato, Romeo Erminia, Bagolan Pietro, Dall'Oglio Luigi, Ceccarelli Stefano, Francalanci Paola, Hermans Dominique, Pietrobattista Andrea, Diamanti Antonella, Torroni Filippo, De Angelis Paola

机构信息

Intestinal Failure Rehabilitation Group, Bambino Gesù Children's Hospital, Rome, Italy.

Intestinal Failure Rehabilitation Group, Bambino Gesù Children's Hospital, Rome, Italy; Department of Pediatrics, University of L'Aquila, L'Aquila, Italy.

出版信息

J Pediatr Surg. 2018 Mar;53(3):483-488. doi: 10.1016/j.jpedsurg.2017.05.030. Epub 2017 Jun 3.

Abstract

BACKGROUND AND AIMS

Anastomotic ulceration (AU) is a rare potential life-threatening complication that may occur after intestinal resection. The diagnosis is often delayed after a long-lasting history of refractory anemia. The pathogenesis remains unknown and there are no established therapies. The aim of the study was to analyze the medical history of children with short bowel syndrome (SBS) who were experiencing AU.

METHODS

Records of SBS children were retrospectively reviewed. Demographics, baseline characteristics, presentation, diagnosis and treatment of AU cases were analyzed.

RESULTS

Eight out of 114 children with SBS were identified as having AU. Mean gestational age was 32.5weeks. Underlying diseases were: 5 necrotising enterocolitis, 2 gastroschisis and 1 multiple intestinal atresia. The mean age at AU diagnosis was 6.5years (diagnosis delay of 35months). All but 2 patients had AU persistency after medical treatment. Endoscopic treatment (2 argon plasma coagulation; 1 platelet-rich fibrin instillation; 2 endoscopic hydrostatic dilations) was effective in 3 out of 5 children. Surgery was required in 3 patients.

CONCLUSIONS

Severe bowel ischemic injury, especially in preterm infant, could predispose to AU development. Medical treatment showed discouraging results. We firstly described that different endoscopic treatment could be attempted before resorting to further surgery.

LEVEL OF EVIDENCE

IV.

摘要

背景与目的

吻合口溃疡(AU)是肠切除术后可能发生的一种罕见的、有潜在生命危险的并发症。在经历长期难治性贫血病史后,诊断往往会延迟。其发病机制尚不清楚,且尚无既定的治疗方法。本研究的目的是分析患有吻合口溃疡的短肠综合征(SBS)儿童的病史。

方法

对短肠综合征儿童的病历进行回顾性分析。分析了吻合口溃疡病例的人口统计学、基线特征、临床表现、诊断和治疗情况。

结果

114例短肠综合征儿童中有8例被诊断为吻合口溃疡。平均胎龄为32.5周。潜在疾病包括:5例坏死性小肠结肠炎、2例腹裂和1例多发性肠闭锁。吻合口溃疡诊断时的平均年龄为6.5岁(诊断延迟35个月)。除2例患者外,所有患者经药物治疗后吻合口溃疡仍持续存在。内镜治疗(2例氩离子凝固术;1例富血小板纤维蛋白滴注;2例内镜下液压扩张)在5例儿童中有3例有效。3例患者需要手术治疗。

结论

严重的肠道缺血性损伤,尤其是早产儿,可能易患吻合口溃疡。药物治疗效果不佳。我们首次描述了在采取进一步手术之前可以尝试不同的内镜治疗方法。

证据级别

四级

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