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小儿患者中与隐性脊柱裂相关的背部中线皮肤体征。

Dorsal midline cutaneous stigmata associated with occult spinal dysraphism in pediatric patients.

作者信息

Sung Hyun Jung, Lee Hyun-Seung

机构信息

Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Korean J Pediatr. 2019 Jan;62(2):68-74. doi: 10.3345/kjp.2018.06744. Epub 2018 Oct 1.

DOI:10.3345/kjp.2018.06744
PMID:30304899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6382965/
Abstract

PURPOSE

To investigate the prevalence of occult spinal dysraphism (OSD) and subsequent neurosurgery in pediatric patients with isolated or combined dorsal midline cutaneous stigmata with or without other congenital malformations.

METHODS

We carried out a retrospective review of patients who underwent sonography or magnetic resonance imaging (MRI) for OSD because of suspicion of dorsal midline cutaneous stigmata (presumed to be a marker for OSD) between January 2012 and June 2017. Information about patient characteristics, physical examination findings, spinal ultrasound and MRI results, neurosurgical notes, and accompanying congenital anomalies was collected.

RESULTS

Totally 250 patients (249 ultrasound and one MRI screening) were enrolled for analysis. Eleven patients underwent secondary MRI examinations. The prevalence of OSD confirmed by an MRI was 2.4% (6 patients including one MRI screening). Five patients (2%) had tethered cord and underwent prophylactic neurosurgery, 3 of whom had a sacrococcygeal dimple and a fibrofatty mass. Prevalence of tethered cord increased as markers associated with a sacrococcygeal dimple increased (0.5% of the isolated marker group, 8.1% of the 2-marker group, and 50% of the 3-marker group). Incidence of OSD with surgical detethering in 17 other congenital anomaly patients was 11.8%, which was higher than the 1.3% in 233 patients without other congenital anomalies.

CONCLUSION

Our results suggest that the presence of dorsal midline cutaneous stigmata, particularly fibrofatty masses, along with a sacrococcygeal dimple is associated with OSD or cord tethering requiring surgery. OSD should be suspected in patients with concurrent occurrence of other congenital anomalies.

摘要

目的

探讨患有孤立性或合并性背部中线皮肤体征且伴有或不伴有其他先天性畸形的儿科患者中隐匿性脊柱裂(OSD)的患病率及后续神经外科手术情况。

方法

我们对2012年1月至2017年6月期间因怀疑背部中线皮肤体征(被认为是OSD的标志物)而接受超声检查或磁共振成像(MRI)以排查OSD的患者进行了回顾性研究。收集了有关患者特征、体格检查结果、脊柱超声和MRI结果、神经外科手术记录以及伴随的先天性异常的信息。

结果

共纳入250例患者(249例超声检查和1例MRI筛查)进行分析。11例患者接受了二次MRI检查。经MRI确诊的OSD患病率为2.4%(6例患者,包括1例MRI筛查患者)。5例患者(2%)患有脊髓拴系并接受了预防性神经外科手术,其中3例有骶尾部酒窝和纤维脂肪肿块。随着与骶尾部酒窝相关的标志物增加,脊髓拴系的患病率也增加(孤立标志物组为0.5%,两个标志物组为8.1%,三个标志物组为50%)。17例其他先天性异常患者中接受手术松解脊髓拴系的OSD发生率为11.8%,高于233例无其他先天性异常患者中的1.3%。

结论

我们的结果表明,背部中线皮肤体征,特别是纤维脂肪肿块,以及骶尾部酒窝的存在与需要手术的OSD或脊髓拴系有关。对于同时发生其他先天性异常的患者应怀疑存在OSD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fec/6382965/ca27b02eabe6/kjp-2018-06744f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fec/6382965/ca27b02eabe6/kjp-2018-06744f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fec/6382965/ca27b02eabe6/kjp-2018-06744f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fec/6382965/ca27b02eabe6/kjp-2018-06744f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fec/6382965/ca27b02eabe6/kjp-2018-06744f1.jpg

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