Stannard C, Knight B K, Sealy R
Br J Ophthalmol. 1985 Oct;69(10):749-53. doi: 10.1136/bjo.69.10.749.
A patient with unilateral hereditary retinoblastoma who was successfully treated at the age of 7 weeks developed a tumour in the pineal region two and a half years later. The initial response to radiation treatment of the latter lesion was not maintained. Subsequent necropsy findings are described. Clinically and pathologically this case represents an example of the recently described trilateral retinoblastoma. The response to treatment after early recognition was disappointing.
一名单侧遗传性视网膜母细胞瘤患者在7周龄时成功接受治疗，两年半后松果体区出现肿瘤。对后一病变的放射治疗初始反应未能维持。描述了随后的尸检结果。从临床和病理角度来看，该病例代表了最近描述的 trilateral retinoblastoma 的一个实例。早期诊断后的治疗反应令人失望。
