Kline L B, Kim J Y, Ceballos R
Ophthalmology. 1985 Aug;92(8):1118-26. doi: 10.1016/s0161-6420(85)33898-8.
Following surgery for pituitary adenoma, radiation therapy is an accepted treatment in reducing tumor recurrence. However, a potential therapeutic complication is delayed radionecrosis of perisellar neural structures, including the optic nerves and chiasm. This particular cause of visual loss, radiation optic neuropathy (RON), has not been emphasized in the ophthalmologic literature. Four cases of RON seen in the past five years are reported. Diagnostic criteria include: (1) acute visual loss (monocular or binocular), (2) visual field defects indicating optic nerve or chiasmal dysfunction, (3) absence of optic disc edema, (4) onset usually within three years of therapy (peak: 1-1 1/2 years), and (5) no computed tomographic evidence of visual pathway compression. Pathologic findings, differential diagnosis and therapy will be discussed in outlining the clinical profile of RON.
垂体腺瘤手术后,放射治疗是降低肿瘤复发的一种公认的治疗方法。然而,一种潜在的治疗并发症是鞍周神经结构(包括视神经和视交叉)的迟发性放射性坏死。这种导致视力丧失的特殊原因,即放射性视神经病变(RON),在眼科文献中尚未得到强调。本文报告了过去五年中见到的4例RON病例。诊断标准包括:(1)急性视力丧失(单眼或双眼),(2)提示视神经或视交叉功能障碍的视野缺损,(3)无视盘水肿,(4)通常在治疗后三年内发病(高峰:1 - 1.5年),以及(5)计算机断层扫描无视觉通路受压的证据。在概述RON的临床特征时,将讨论病理表现、鉴别诊断和治疗方法。