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脊髓栓系综合征与肛门直肠畸形:病例系列

Tethered Cord and Anorectal Malformations: A Case Series.

作者信息

Destro Francesca, Canazza Lorena, Meroni Milena, Selvaggio Giorgio, Parazzini Cecilia, Valentini Laura, Riccipetitoni Giovanna

机构信息

Department of Pediatric Surgery, Ospedale dei Bambini Vittore Buzzi, Milano, Lombardia, Italy.

Department of Neurosurgery, Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta, Milano, Lombardia, Italy.

出版信息

Eur J Pediatr Surg. 2018 Dec;28(6):484-490. doi: 10.1055/s-0037-1606844. Epub 2017 Sep 25.

Abstract

INTRODUCTION

The clinical manifestation of a stretched low-lying cone (LLC) is represented by the tethered cord syndrome (TCS) with cutaneous, urologic, neurologic, and orthopaedic dysfunctions. TC is frequently found in patients with anorectal malformations (ARMs). The aim of our article is to report a series of patients affected by LLC and ARMs and evaluate their management and long-term follow-up results.

MATERIALS AND METHODS

We performed a retrospective analysis over a period of 15 years including patients with ARM and TC and excluding those with severe polymalformations. We collected information related to the types of malformations and demographic data. We analyzed their management (perinatal protocol, radiological investigations, surgery, and multidisciplinary follow-up). QOL was assessed through the International Classification of Functioning, Disability, and Health for Children and Youth (ICF-CY).

RESULTS

Thirty-three patients among 210 ARM cases had TC (16%). Eleven of them underwent neurosurgery. One patient had retethering; out of 11 patients, 4 remained stable and 6 improved after surgery (UDS normalization and resolution of symptoms). At a mean follow-up of 10 years, four patients were on clean intermittent catheterization and five on the Peristeen transanal irrigation. The majority of patients were defined as 3 (from 1-bad to 5-excellent) for their physical and mental state.

CONCLUSION

The use of MRI is considered to complete the ARM screening in detecting TC. The multidisciplinary approach is crucial and helps in defining the management of patients. In fact, it is not clear how the features of ARM and TC affect each other. The selection of cases for surgery should take into account the critical elements.

摘要

引言

低位圆锥(LLC)拉伸的临床表现为伴有皮肤、泌尿、神经和骨科功能障碍的脊髓拴系综合征(TCS)。脊髓拴系在肛门直肠畸形(ARM)患者中很常见。我们文章的目的是报告一系列受LLC和ARM影响的患者,并评估他们的治疗及长期随访结果。

材料与方法

我们对15年期间的患者进行了回顾性分析,纳入患有ARM和脊髓拴系的患者,排除有严重多发畸形的患者。我们收集了与畸形类型和人口统计学数据相关的信息。我们分析了他们的治疗(围产期方案、影像学检查、手术和多学科随访)。通过儿童和青少年功能、残疾与健康国际分类(ICF-CY)评估生活质量。

结果

210例ARM病例中有33例患有脊髓拴系(16%)。其中11例接受了神经外科手术。1例患者进行了再次拴系松解;在11例患者中,4例术后保持稳定,6例有所改善(尿动力学检查正常化且症状缓解)。平均随访10年时,4例患者进行清洁间歇性导尿,5例患者采用经肛门Peristeen冲洗。大多数患者的身体和精神状态被评定为3级(从1级差到5级优)。

结论

MRI的使用被认为可完善ARM筛查以检测脊髓拴系。多学科方法至关重要,有助于确定患者的治疗方案。实际上,尚不清楚ARM和脊髓拴系的特征如何相互影响。手术病例的选择应考虑关键因素。

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