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影像学表现为“囊性”鞍上肿块的恶性视神经胶质瘤:病例报告及文献复习

Malignant optic glioma presenting radiologically as a "cystic" suprasellar mass: case report and review of the literature.

作者信息

Barbaro N M, Rosenblum M L, Maitland C G, Hoyt W F, Davis R L

出版信息

Neurosurgery. 1982 Dec;11(6):787-9. doi: 10.1227/00006123-198212000-00011.

Abstract

The diagnosis of malignant glioma of the optic nerves and chiasm may be difficult because these rare lesions may mimic other suprasellar lesions. We report a case of glioblastoma multiforme of the optic chiasm in which the appearance of the lesion on computed tomographic (CT) scan was consistent with that of craniopharyngioma or cystic pituitary adenoma. We suggest that malignant optic glioma should be considered in the differential diagnosis of an adult with progressive visual loss of rapid onset, even when ophthalmological examination strongly suggests extrinsic compression of the anterior optic pathways and when the CT scan apparently indicates a cystic mass lesion.

摘要

视神经和视交叉恶性胶质瘤的诊断可能较为困难,因为这些罕见病变可能与其他鞍上病变相似。我们报告一例视交叉多形性胶质母细胞瘤病例,其计算机断层扫描(CT)表现与颅咽管瘤或囊性垂体腺瘤一致。我们建议,对于快速出现进行性视力丧失的成年人,即使眼科检查强烈提示视神经前通路存在外在压迫且CT扫描明显显示为囊性肿块病变,在鉴别诊断时也应考虑恶性视神经胶质瘤。

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