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脊髓神经管囊肿:相关发育异常及手术入路的理论依据

Spinal neurenteric cysts: Associated developmental anomalies and rationale of surgical approaches.

作者信息

Shukla Mukesh, Behari Sanjay, B Guruprasad, Das Kuntal Kanti, Mehrotra Anant, Srivastava Arun Kumar, Sahu Rabi Narayan, Jaiswal Awadhesh K, Jain Manoj

机构信息

Department of Neurosurgery, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, 226014, India.

出版信息

Acta Neurochir (Wien). 2015 Sep;157(9):1601-10. doi: 10.1007/s00701-015-2484-7. Epub 2015 Jul 26.

Abstract

BACKGROUND

Neurenteric cysts (NC) occur due to failure of separation of neurectoderm from endoderm at the 3rd week of embryogenesis. This study focuses on key clinico-radiological features of NCs, with emphasis on surgical nuances involved in resecting anteriorly placed NC, especially at the foramen magnum (FM).

METHOD

Sixteen consecutive patients having a spinal NC were included. Their clinico-radiological status, surgical nuances and follow-up status were noted.

RESULTS

The duration of spasticity/paraparesis/quadriparesis ranged from 15 days to 48 months. Twelve patients had an intradural extramedullary (IDEM; nine anterior and three anterolateral) cyst and four had an intramedullary (IM) cyst. Six of them had an anteriorly placed FM lesion (five IDEM and one IM). Amongst ten subaxial NCs, four were anterior, two antero-lateral and one postero-lateral; three were IM. Three patients had the characteristic stigmata of occult spinal dysraphism: two, a large mesenteric cyst, and one, a posterior mediastinal cyst. Excision was total in 13 patients. Subtotal excision of tumour capsule was performed for two recurrent cysts and an IM cyst. A far lateral approach was adopted for anteriorly placed FM lesions and posterior laminectomy for subaxial lesions. Histopathology revealed eight type A cysts, four type B cysts and four type C cysts. At follow-up (range, 8 months to 12 years; median, 60 ± 45.84 months), complete neurological recovery occurred in seven patients; six patients had persistent spasticity but only minor disability; two patients had difficulty in walking; and one patient with an anteriorly placed thoracic recurrent NC had sustained neurological deterioration.

CONCLUSIONS

Surgical difficulties in addressing NCs are related to their anterior or IM location, presence of adhesions and inability to dissect the tumour capsule from the spinal cord due to fibrous or lipomatous connections. The associated developmental anomalies must be specifically sought and addressed.

摘要

背景

神经肠囊肿(NC)是由于胚胎发育第3周时神经外胚层与内胚层分离失败所致。本研究聚焦于NC的关键临床放射学特征,重点关注切除前方位置的NC(尤其是枕骨大孔处的NC)所涉及的手术细节。

方法

纳入16例连续性脊髓NC患者。记录他们的临床放射学状况、手术细节及随访情况。

结果

痉挛/双下肢轻瘫/四肢瘫的持续时间为15天至48个月。12例患者有硬膜内髓外(IDEM;9例位于前方,3例位于前外侧)囊肿,4例有髓内(IM)囊肿。其中6例有位于前方的枕骨大孔病变(5例IDEM和1例IM)。在10例颈椎以下的NC中,4例位于前方,2例位于前外侧,1例位于后外侧;3例为IM。3例患者有隐性脊柱裂的特征性表现:2例有巨大肠系膜囊肿,1例有后纵隔囊肿。13例患者肿瘤完全切除。对2例复发性囊肿和1例IM囊肿进行了肿瘤囊壁次全切除。对于前方位置的枕骨大孔病变采用远外侧入路,对于颈椎以下病变采用后路椎板切除术。组织病理学显示8例A型囊肿,4例B型囊肿和4例C型囊肿。随访(范围8个月至12年;中位时间60±45.84个月)时,7例患者神经功能完全恢复;6例患者有持续性痉挛但仅有轻微残疾;2例患者行走困难;1例前方位置的胸段复发性NC患者出现持续性神经功能恶化。

结论

处理NC的手术困难与其前方或髓内位置、粘连的存在以及由于纤维或脂肪瘤连接而无法从脊髓上分离肿瘤囊壁有关。必须特别查找并处理相关的发育异常情况。

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