Kaiser-Kupfer M I, Kupfer C, Rodrigues M M
Ophthalmology. 1981 Jan;88(1):89-93. doi: 10.1016/s0161-6420(81)35071-4.
A 57-year-old woman with metastatic breast carcinoma treated by surgery and high-dosage tamoxifen chemotherapy developed tamoxifen retinopathy characterized by white superficial refractile retinal lesions primarily in the paramacular area. At postmortem examination, the retinal lesions seen clinically were identified as being 3 to 10 microns in diameter in the macular area, and 30 to 35 microns in diameter in the paramacular area. The lesions were confined to the nerve fiber layer and inner plexiform layer and stained positive with stains for glycosaminoglycans. Electron microscopic examination revealed that the smaller lesions were intracellular and the larger lesions extracellular. The lesions were composed of randomly oriented branching electron dense 6-nm filaments accompanied by occasional electron dense coated vesicles measuring 60 to 70 nn in diameter. The lesions appeared to be occurring in axons and seemed to represent products of axonal degeneration.
一名57岁的转移性乳腺癌女性患者接受了手术和高剂量他莫昔芬化疗,出现了他莫昔芬视网膜病变,其特征为白色浅表性可折射视网膜病变,主要位于黄斑旁区域。尸检时,临床所见的视网膜病变在黄斑区直径为3至10微米,在黄斑旁区域直径为30至35微米。病变局限于神经纤维层和内网状层,用糖胺聚糖染色呈阳性。电子显微镜检查显示,较小的病变位于细胞内,较大的病变位于细胞外。病变由随机排列的分支状电子致密6纳米细丝组成,偶尔伴有直径为60至70纳米的电子致密被膜小泡。病变似乎发生在轴突中,似乎代表轴突变性的产物。