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[马尾综合征揭示的脊髓神经管囊肿]

[Spinal neurenteric cyst revealed by a cauda equina syndrome].

作者信息

Rougerie C, Chazerain P, Arthuis F, Chicheportiche V, Ziza J M

机构信息

Service de Rhumatologie et Médecine interne, Hôpital de la Croix Saint-Simon, Paris.

出版信息

Presse Med. 1999 Feb 6;28(5):229-30.

PMID:10076597
Abstract

BACKGROUND

Intraspinal neurenteric cysts are exceptional formations which develop from incomplete separation of the neural tube and the endodermis during the third week of gestation. Symptoms generally appear before the age of 40 years and are associated with spinal malformations. Most neurenteric cysts lie in an extra-spinal position in the lower cervical and upper dorsal spine. We report a case involving the cauda equina with no associated spinal lesion.

CASE REPORT

A 63-year-old woman was admitted for low back pain and right L3 radiculalgia triggered by exertion. Urinary disorders had developed over the preceding year. Physical examination found a spinal syndrome with hypoesthesia of the right para-anal area, an atonic anal sphincter and a globular bladder. Plain films showed a widened interpedicular space between L1 and L2 interpreted as the consequence of an expansive intraspinal lesion. Saccoradiculography led to the diagnosis of an intradural lesion involving L1 and L2. At magnetic resonance imaging, the lesion's signal intensity was similar to cerebrospinal fluid on T1 and T2 sequences, deforming the cauda equina and displacing the nerve roots. Surgical resection of the cyst was incomplete due to adherences to several roots and was followed by persistent radiculalgia and sphincter disorders.

DISCUSSION

This case demonstrates an exceptional cause of cauda equina syndrome. Fissuration or rupture of the cyst might explain symptom exacerbation following trauma. Magnetic resonance imagining can confirm the cystic nature of the intradural lesion and help guide surgery. Resection is often incomplete with the risk of long-term recurrence.

摘要

背景

椎管内神经肠囊肿是一种罕见的病变,它是在妊娠第三周神经管与内胚层未完全分离而形成的。症状通常在40岁之前出现,且与脊柱畸形有关。大多数神经肠囊肿位于下颈椎和上胸椎的椎管外位置。我们报告一例累及马尾神经且无相关脊柱病变的病例。

病例报告

一名63岁女性因劳累引发的腰痛和右侧L3神经根痛入院。在过去一年中出现了泌尿系统疾病。体格检查发现脊柱综合征,右侧肛门旁区域感觉减退,肛门括约肌张力缺失和球形膀胱。X线平片显示L1和L2之间的椎弓根间距增宽,被解释为椎管内占位性病变的结果。脊髓造影诊断为累及L1和L2的硬膜内病变。在磁共振成像中,病变在T1和T2序列上的信号强度与脑脊液相似,使马尾神经变形并使神经根移位。由于囊肿与几根神经根粘连,手术切除不完全,术后持续存在神经根痛和括约肌功能障碍。

讨论

该病例显示了马尾神经综合征的一种罕见病因。囊肿的裂开或破裂可能解释了创伤后症状加重的原因。磁共振成像可以确认硬膜内病变的囊性性质并有助于指导手术。切除往往不完全,存在长期复发的风险。

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Presse Med. 1999 Feb 6;28(5):229-30.
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