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表现为类固醇反应性视神经病变的原发性脑网状细胞肉瘤

Primary reticulum cell sarcoma of the brain presenting as steroid-responsive optic neuropathy.

作者信息

Purvin V, Van Dyk H J

出版信息

J Clin Neuroophthalmol. 1984 Mar;4(1):15-23. doi: 10.3109/01658108409019491.

DOI:10.3109/01658108409019491
PMID:6233304
Abstract

A 23-year-old woman presented with subacute monocular visual loss clinically resembling optic neuritis. CT scan revealed a cerebellar mass, biopsy of which led to the diagnosis of reticulum cell sarcoma (RCS). Corticosteroid therapy resulted in improvement of vision and a decrease in disc edema; this resolution was documented radiographically. While optic nerve involvement is sometimes seen in association with systemic lymphoproliferative disease, optic neuropathy as a manifestation of primary cerebral RCS is rare.

摘要

一名23岁女性出现亚急性单眼视力丧失,临床症状类似视神经炎。CT扫描显示小脑有一肿块,对其进行活检后诊断为网状细胞肉瘤(RCS)。皮质类固醇治疗使视力得到改善,视盘水肿减轻;影像学检查记录了这种好转情况。虽然视神经受累有时与全身性淋巴增殖性疾病相关,但原发性脑RCS表现为视神经病变的情况较为罕见。

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