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小儿人群中的骶管内脊膜膨出。

Intrasacral meningocele in the pediatric population.

作者信息

Lohani Subash, Rodriguez Diana P, Lidov Hart G W, Scott R Michael, Proctor Mark R

机构信息

Department of Neurosurgery, Boston Children’s Hospital, Boston, Massachusetts, USA.

出版信息

J Neurosurg Pediatr. 2013 Jun;11(6):615-22. doi: 10.3171/2013.3.PEDS12519. Epub 2013 Apr 19.

Abstract

OBJECT

Intrasacral meningoceles are rare cystic lesions that can cause focal compression within the bony sacral canal. Their mechanisms are poorly understood, but most intrasacral meningoceles appear to be intrasacral extradural cysts caused by arachnoid herniating through a small dural defect in the caudal end of the thecal sac. As opposed to perineural cysts, they are not associated with an exiting nerve root. When symptomatic, they can cause sacral pain or sacral nerve root dysfunction due to local compression.

METHODS

This is a retrospective series from Boston Children's Hospital. All patients in whom symptomatic intrasacral meningocele that required surgical treatment was diagnosed between May 1994 and March 2011 were included in the study. Spine MRI was the diagnostic modality of choice. All patients underwent sacral exploration, with ligation and obliteration of the cyst. Resected cyst wall was subjected to pathological examination.

RESULTS

There were 13 patients (11 boys and 2 girls) who underwent operation for intrasacral meningocele. The median age was 8 years (range 5 months-16 years). The most common presenting symptom was back pain (in 5) often described as deep tail bone pain, followed by urinary incontinence (3) and constipation (2). Three patients had evidence of associated tethered cord on MRI studies. Four patients were asymptomatic and their diagnosis was made following imaging for other reasons; they were surgically treated because of the increasing size of the lesion or association with other congenital lesions. Most patients had symptomatic improvement after surgery.

CONCLUSIONS

Intrasacral meningoceles are rare lesions that may result from a congenital dural weakness and a resultant arachnoid diverticulum. They present in childhood either incidentally or with symptoms secondary to nerve root compression. Identification of the point of herniation through the dura mater and ligation of the lesion provides cyst cure and resolution of symptoms in most patients.

摘要

目的

骶管内脊膜膨出是一种罕见的囊性病变,可导致骶管内局部压迫。其发病机制尚不清楚,但大多数骶管内脊膜膨出似乎是由于蛛网膜通过硬脊膜囊尾端的一个小硬脑膜缺损疝出而形成的骶管内硬膜外囊肿。与神经束膜囊肿不同,它们与穿出的神经根无关。有症状时,由于局部压迫,可导致骶部疼痛或骶神经根功能障碍。

方法

这是一项来自波士顿儿童医院的回顾性研究系列。研究纳入了1994年5月至2011年3月期间诊断为有症状且需要手术治疗的骶管内脊膜膨出的所有患者。脊柱磁共振成像(MRI)是首选的诊断方法。所有患者均接受了骶部探查,对囊肿进行结扎和闭塞。切除的囊肿壁进行病理检查。

结果

有13例患者(11例男孩和2例女孩)接受了骶管内脊膜膨出手术。中位年龄为8岁(范围5个月至16岁)。最常见的首发症状是背痛(5例),常描述为尾骨深部疼痛,其次是尿失禁(3例)和便秘(2例)。3例患者在MRI检查中有脊髓栓系的证据。4例患者无症状,因其他原因进行影像学检查时确诊;由于病变增大或与其他先天性病变相关,对其进行了手术治疗。大多数患者术后症状有所改善。

结论

骶管内脊膜膨出是一种罕见的病变,可能由先天性硬脑膜薄弱和由此产生的蛛网膜憩室引起。它们在儿童期可偶然出现,或因神经根受压而出现症状。识别硬脑膜的疝出点并结扎病变可使大多数患者囊肿治愈且症状缓解。

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