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颈椎硬脊膜内髓外血管母细胞瘤:病例报告及文献综述

Intradural Extramedullary Hemangioblastoma of the Cervical Spine: Case Report and Literature Review.

作者信息

Fanous Andrew, Mugge Luke, Kurzejewski Kelly, Cournoyer April, Ziu Mateo

机构信息

Neurological Surgery, Inova Fairfax Hospital, Falls Church Virginia , USA.

Department of Neurosurgery, Inova Neuroscience and Spine Institute, Falls Church, USA.

出版信息

Cureus. 2022 May 18;14(5):e25125. doi: 10.7759/cureus.25125. eCollection 2022 May.

Abstract

Hemangioblastomas are uncommon in the spine, accounting for less than 3% of all spinal cord tumors and occurring even more rarely in the intradural extramedullary vicinity. We present a unique case report of an intradural extramedullary hemangioblastoma. A 62-year-old man presented with a five-month history of neck pain radiating to the left arm. A magnetic resonance imaging (MRI) of the cervical spine revealed a left paracentral contrast-enhancing intradural extramedullary lesion at the C4-C5 level. Surgical options were discussed, and surgery was performed via a posterolateral approach. The lateral masses and facets at the C4 and C5 levels were drilled and the tumor was encountered ventral to the spinal cord. There were multiple nerve roots adherent to the tumor capsule. The tumor was highly vascularized. Analysis revealed a highly vascular lesion with vacuolated tumor cells, positive for inhibin and S100 stains, consistent with a diagnosis of hemangioblastoma. The patient remains intact throughout the post-operative period. Few studies have reported intradural extramedullary spinal hemangioblastomas and purely extramedullary spinal hemangioblastomas of the neuraxis are far less common. Most cases occur in the Japanese population and in patients over the age of 50. By location, extramedullary hemangioblastomas involving the thoracic spine occur in women, while those occurring in men are restricted to the cervical spine or conus medullaris. Complete resection remains the treatment of choice.

摘要

血管母细胞瘤在脊柱中并不常见,占所有脊髓肿瘤的比例不到3%,在硬脊膜内髓外区域更为罕见。我们报告了一例独特的硬脊膜内髓外血管母细胞瘤病例。一名62岁男性,有五个月的颈部疼痛并向左上肢放射的病史。颈椎磁共振成像(MRI)显示在C4 - C5水平有一个左侧中央旁硬脊膜内髓外强化病变。讨论了手术方案,并通过后外侧入路进行了手术。对C4和C5水平的侧块和小关节进行钻孔,在脊髓腹侧发现肿瘤。有多个神经根附着于肿瘤包膜。肿瘤血管丰富。分析显示为血管丰富的病变,肿瘤细胞有空泡,抑制素和S100染色阳性,符合血管母细胞瘤的诊断。患者术后情况良好。很少有研究报道硬脊膜内髓外脊髓血管母细胞瘤,而神经轴纯粹的髓外脊髓血管母细胞瘤更为少见。大多数病例发生在日本人群以及50岁以上的患者中。按部位而言,累及胸椎的髓外血管母细胞瘤多见于女性,而男性的则局限于颈椎或圆锥。完整切除仍然是首选的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40c2/9205786/4e254d32db70/cureus-0014-00000025125-i01.jpg

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