Abramson D H, McCormick B, Fass D, Ellsworth R M, Gerardi C, Servodidio C A, Romanella A
Ophthalmic Oncology Center, New York Hospital Cornell Medical Center, New York.
Cancer. 1991 Jun 1;67(11):2753-5. doi: 10.1002/1097-0142(19910601)67:11<2753::aid-cncr2820671107>3.0.co;2-f.
A retrospective analysis of 50 patients with retinoblastoma was undertaken to determine the appearance of intraocular retinoblastoma that had received external beam radiation a minimum of 10 years previously. Of the 91 tumors found in 59 eyes, 76 (84%) continued to be ophthalmoscopically visible after 10 years. The most common ophthalmoscopic appearance was a Type III regression pattern. The type of radiation regression pattern correlated with the pretreatment volume of the tumor. The largest tumors (mean, 10.0 disc diameter [dd]) became Type I regression patterns, whereas the smallest tumors (mean, 1.0 dd) completely disappeared. This represents the first long-term follow-up of the intraocular status of radiated retinoblastoma.
对50例视网膜母细胞瘤患者进行了回顾性分析,以确定至少在10年前接受过外照射放疗的眼内视网膜母细胞瘤的表现。在59只眼中发现的91个肿瘤中,76个(84%)在10年后通过检眼镜仍可见。最常见的检眼镜表现为III型消退模式。放疗消退模式的类型与肿瘤的治疗前体积相关。最大的肿瘤(平均10.0视盘直径[dd])呈现I型消退模式,而最小的肿瘤(平均1.0 dd)则完全消失。这是对接受放疗的视网膜母细胞瘤眼内状况的首次长期随访。