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在对单纯性小儿腰骶部脂肪瘤进行检查时,无需进行全脊柱磁共振成像。一项单机构回顾性研究。

Whole spine MRI is not required in investigating uncomplicated paediatric lumbosacral lipoma. A retrospective single-institution review.

作者信息

Layard Horsfall Hugo, Chari Aswin, Huttunen Terhi, Simcock Clare, D'Arco Felice, Thompson Dominic

机构信息

Department of Neurosurgery, Great Ormond Street Hospital for Children, London, UK.

Division of Neurosurgery, Department of Clinical Neurosciences, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.

出版信息

Childs Nerv Syst. 2019 Nov;35(11):2163-2169. doi: 10.1007/s00381-019-04373-z. Epub 2019 Sep 9.

Abstract

PURPOSE

Lumbosacral lipoma (LSL) is a severe occult spinal dysraphism, frequently associated with neurological, urological and orthopaedic complications. Whole spine imaging is typically performed to identify concomitant, but spatially separate, congenital anomalies. Our hypothesis: the incidence of additional, clinically significant abnormalities of the neuraxis is low; thus, imaging should be optimised at the lumbosacral region. We aim to assess the prevalence and relevance of LSL-associated lesions.

METHOD

A single-centre, retrospective, radiological review using a prospectively maintained operative database.

INCLUSION CRITERIA

children (< 16 years) with confirmed diagnosis of LSL and received whole spine MRI. Fatty filum, syndromic cases and cutaneous stigmata above lesion level were excluded. Data was extracted from radiological imaging, reports and clinical correspondence.

RESULTS

One hundred twelve patients (40:72, M:F) aged 0.5 years (0.2-2.7) (median ± IQR) with LSL had whole spine MRI between 2001 and 2017. Classification of LSL: transitional 48 (43%); dorsal 30 (27%); caudal 28 (25%) and chaotic 6 (5%). Additional anomalies included syringohydromyelia 44 (39%), subcutaneous tract 19 (17%), abnormal vertebral segmentation 18 (16%), dermoid cyst 1 and 1 Chiari I deformity. There were no Chiari II malformations. No child required surgery for an associated lesion. Binary logistic regression revealed no factors associated with predicting secondary lesions.

CONCLUSIONS

In congenital LSL, additional anomalies of the neuraxis are typically loco-regional rather than pan-CNS and additional lesions are rarely clinically significant. The loco-regional distribution of anomalies suggests that only lumbosacral spinal imaging is required in the initial evaluation of LSL. Such a policy would lessen the anaesthetic/sedation time for children and reduce imaging cost per patient. MRI protocols could be refined to optimise imaging quality at the region of interest.

摘要

目的

腰骶部脂肪瘤(LSL)是一种严重的隐匿性脊柱发育异常,常伴有神经、泌尿和骨科并发症。通常进行全脊柱成像以识别同时存在但在空间上分离的先天性异常。我们的假设:神经轴上其他具有临床意义的异常发生率较低;因此,应在腰骶部区域优化成像。我们旨在评估与LSL相关病变的患病率和相关性。

方法

使用前瞻性维护的手术数据库进行单中心、回顾性放射学评估。

纳入标准

确诊为LSL并接受全脊柱MRI检查的儿童(<16岁)。排除脂肪终丝、综合征病例和病变水平以上的皮肤体征。数据从放射学影像、报告和临床通信中提取。

结果

2001年至2017年间,112例年龄为0.5岁(0.2 - 2.7岁)(中位数±四分位间距)的LSL患者接受了全脊柱MRI检查,其中男性40例,女性72例。LSL的分类:过渡型48例(43%);背侧型30例(27%);尾侧型28例(25%)和混合型6例(5%)。其他异常包括脊髓空洞症44例(39%)、皮下通道19例(17%)、椎体节段异常18例(16%)、皮样囊肿1例和Chiari I畸形1例。无Chiari II畸形。没有儿童因相关病变需要手术。二元逻辑回归显示没有与预测继发性病变相关的因素。

结论

在先天性LSL中,神经轴的其他异常通常是局部区域的,而非全中枢神经系统的,且其他病变很少具有临床意义。异常的局部区域分布表明,在LSL的初始评估中仅需进行腰骶部脊柱成像。这样的策略将减少儿童的麻醉/镇静时间,并降低每位患者的成像成本。MRI方案可进行优化,以提高感兴趣区域的成像质量。

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