Garg Nitin, Sampath S, Yasha T C, Chandramouli B A, Devi B Indira, Kovoor Jerry M E
Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.
Br J Neurosurg. 2008 Apr;22(2):241-51. doi: 10.1080/02688690701818919.
Spinal neurenteric cysts are intradural cystic lesions. These represent a part of the spectrum of developmental anomalies. These are rare lesions. Most of the data in literature is review of case reports. This made us evaluate our results of 23 cases and review the literature. This is a retrospective study of 23 patients managed at our institute over 20 years. The slides were retrieved and histopathological features studied. Twenty patients were less than 30 years old and 21 were males. Follow-up was available for 21 patients with mean duration of 71 months (range 2 months to 23 years). The typical presentation was backache with progressive neurological deficits pertaining to the level. Atypical presentations as acute onset, recurrent episodic events and aseptic meningitis were also noted. The cervicothoracic region was the most common site. 16 patients had cyst in intradural extramedullary plane and seven had intramedullary location. Associated vertebral anomalies as hemivertebrae, Klippel-Feil and spina bifida were noted in seven patients. There were two histological types of cysts with no correlation between the type of cysts and associated vertebral anomalies and extent of outcome. Partial excision though had higher risk of recurrence, was not associated with poorer outcome. Dorsal approach is an acceptable route with reasonably good results for this lesion. Spinal neurenteric cysts present at younger age with varied clinical presentations. These are commonly located intradurally ventral to the cord. Histological types have no effect on the outcome. Total excision is the choice of treatment. However, partial excision is a feasible option in intramedullary lesions and when significant adhesions occur. Although associated with higher risk of recurrence, the outcome is still good in these patients on re-excision.
脊髓神经管囊肿是硬脊膜内囊性病变。这些病变属于发育异常谱系的一部分。它们是罕见病变。文献中的大多数数据是病例报告综述。这促使我们评估我们23例病例的结果并回顾文献。这是一项对我们研究所20年来收治的23例患者的回顾性研究。检索了切片并研究了组织病理学特征。20例患者年龄小于30岁,21例为男性。21例患者有随访资料,平均随访时间为71个月(范围2个月至23年)。典型表现为背痛并伴有与病变水平相关的进行性神经功能缺损。也注意到非典型表现,如急性起病、反复发作的发作性事件和无菌性脑膜炎。颈胸段是最常见的部位。16例患者的囊肿位于硬脊膜外髓外平面,7例位于髓内。7例患者存在相关的椎体异常,如半椎体、颈椎融合和脊柱裂。囊肿有两种组织学类型,囊肿类型与相关椎体异常及预后程度之间无相关性。尽管部分切除复发风险较高,但与较差的预后无关。后路手术是治疗该病变的一种可接受途径,效果相当不错。脊髓神经管囊肿发病年龄较轻,临床表现多样。它们通常位于硬脊膜内脊髓腹侧。组织学类型对预后无影响。全切除是首选治疗方法。然而,对于髓内病变以及出现明显粘连时,部分切除也是一种可行的选择。尽管部分切除与较高的复发风险相关,但再次切除后这些患者的预后仍然良好。