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视神经血管母细胞瘤:病例报告

Hemangioblastoma of the optic nerve: case report.

作者信息

Kerr D J, Scheithauer B W, Miller G M, Ebersold M J, McPhee T J

机构信息

Department of Pathology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Neurosurgery. 1995 Mar;36(3):573-80; discussion 580-1. doi: 10.1227/00006123-199503000-00017.

Abstract

An optic nerve hemangioblastoma arising in the optic nerve of a patient with von Hippel-Lindau syndrome is reported. This represents the 10th published example of a hemangioblastoma arising at this site, the second description of the magnetic resonance imaging features of a hemangioblastoma at this location, and the second patient from whom an optic nerve hemangioblastoma has been removed with the goal of preserving the optic nerve as well as vision. A majority of these optic nerve hemangioblastomas have arisen in patients with von Hippel-Lindau syndrome. All patients experienced progressive loss of vision either to blindness or surgical intervention, although a vast majority of the lesions were sharply demarcated from the adjacent nerve and, thus, potentially resectable. Optic nerve hemangioblastomas are a rare cause of blindness but potentially preventable when treated with a conservative surgical approach aided by neuroimaging guidance. The recognition of discordance between the degree of vision loss and the extent or progression of a retinal hemangioblastoma may be an important clue to diagnosis in the patient with von Hippel-Lindau syndrome.

摘要

报告了1例发生于冯·希佩尔-林道综合征患者视神经的视神经成血管细胞瘤。这是该部位第10例已发表的成血管细胞瘤病例,是该部位成血管细胞瘤磁共振成像特征的第2次描述,也是第2例以保留视神经及视力为目的切除视神经成血管细胞瘤的患者。这些视神经成血管细胞瘤大多发生于冯·希佩尔-林道综合征患者。所有患者均经历了视力逐渐丧失直至失明或接受手术干预,尽管绝大多数病变与相邻神经界限清晰,因此有可能切除。视神经成血管细胞瘤是导致失明的罕见原因,但在神经影像引导下采用保守手术方法治疗时有可能预防。认识到视网膜成血管细胞瘤导致的视力丧失程度与病变范围或进展情况不一致,可能是冯·希佩尔-林道综合征患者诊断的重要线索。

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