Suppr超能文献

伴有蛛网膜下腔出血病史的颈椎血管母细胞瘤。

Cervical hemangioblastoma with a past history of subarachnoid hemorrhage.

作者信息

Minami M, Hanakita J, Suwa H, Suzui H, Fujita K, Nakamura T

机构信息

Department of Neurosurgery, Shizuoka General Hospital, Japan.

出版信息

Surg Neurol. 1998 Mar;49(3):278-81. doi: 10.1016/s0090-3019(97)00196-1.

Abstract

BACKGROUND

Subarachnoid hemorrhage (SAH) with a spinal origin is a rare clinical entity. The most common source of SAH is an arteriovenous malformation. Only six cases of spinal hemangioblastomas causing SAH have been reported.

CASE DESCRIPTION

This 48-year-old man had experienced severe headache 12 years earlier, which was diagnosed as SAH by computed tomography (CT) scan and lumbar puncture. However, cerebral angiography could not detect either aneurysm or arteriovenous malformation. Thereafter, he spent an uneventful life until he was incidentally diagnosed with a cervical tumor on magnetic resonance imaging (MRI) study for Meniere's disease. The tumor was situated at the cervicomedullary junction, and fed by the left vertebral artery. Histologic findings of the tumor showed features typical of hemangioblastoma.

CONCLUSIONS

We describe a case of cervical spinal extramedullary hemangioblastoma with a past history of SAH. In our case, the SAH of 12 years ago perhaps occurred from the cervicomedullary junction hemangioblastoma. Since the etiology of SAH could not be detected at the first angiography, not only follow-up reangiography, but also MRI of the spinal cord and spinal angiography could have played an important role.

摘要

背景

脊髓源性蛛网膜下腔出血(SAH)是一种罕见的临床病症。SAH最常见的病因是动静脉畸形。仅有6例脊髓血管母细胞瘤导致SAH的病例报道。

病例描述

该48岁男性12年前曾经历严重头痛,经计算机断层扫描(CT)及腰椎穿刺诊断为SAH。然而,脑血管造影未发现动脉瘤或动静脉畸形。此后,他一直生活平稳,直至因梅尼埃病行磁共振成像(MRI)检查时意外发现颈椎肿瘤。肿瘤位于颈髓交界处,由左椎动脉供血。肿瘤组织学检查结果显示为典型的血管母细胞瘤特征。

结论

我们报告一例有SAH病史的颈椎髓外血管母细胞瘤病例。在我们的病例中,12年前的SAH可能源于颈髓交界区血管母细胞瘤。由于首次血管造影未能检测出SAH的病因,因此不仅随访复查血管造影,脊髓MRI及脊髓血管造影也可能发挥了重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验