MacKay C J, Abramson D H, Ellsworth R M
Arch Ophthalmol. 1984 Mar;102(3):391-6. doi: 10.1001/archopht.1984.01040030309025.
Of 23 cases of metastatic retinoblastoma treated between 1922 and 1979, seven had metastases limited to the cranial vault and 13 had cranial metastases plus distant metastases. Globe pathology showed invasion of the optic nerve and/or the choroid in all but two patients, but was not predictive of the metastatic pattern. Initial signs of metastases were neurologic impairment and an orbital or body mass; first symptoms were anorexia or weight loss, vomiting, and headache. Most cases occurred by 3 years of age. Death occurred within 5.8 months on the average, despite therapy. Useful tests for determining the extent of disease were bone marrow aspiration, lumbar puncture, skull films, EEG, and brain scan. Computed tomographic scans of the head, bone scans, bone marrow aspiration, automated blood chemistry analysis, and lumbar puncture with immediate ethyl alcohol processing should prove to be useful to detect metastatic disease.
在1922年至1979年间接受治疗的23例转移性视网膜母细胞瘤病例中,7例转移局限于颅顶,13例有颅转移加远处转移。除2例患者外,眼球病理显示所有患者均有视神经和/或脉络膜侵犯,但这并不能预测转移模式。转移的初始体征为神经功能损害以及眼眶或身体肿块;首发症状为厌食或体重减轻、呕吐和头痛。大多数病例发生在3岁之前。尽管接受了治疗,但平均在5.8个月内死亡。用于确定疾病范围的有用检查包括骨髓穿刺、腰椎穿刺、颅骨平片、脑电图和脑部扫描。头部计算机断层扫描、骨扫描、骨髓穿刺、自动血液化学分析以及立即进行乙醇处理的腰椎穿刺,应可证明对检测转移性疾病有用。