Zimmerman R A, Bilaniuk L T
J Comput Tomogr. 1979 Dec;3(4):251-7. doi: 10.1016/0149-936x(79)90028-6.
Six patients with histologically proven retinoblastomas were examined by computed tomography, two at the time of initial diagnosis and four from 2 to 30 years following treatment, which consisted of radiation therapy alone or with surgery. The spectrum of computed tomographic findings includes: calcified retinal tumor, intracranial subarachnoid spread of tumor, radiation-induced tumors (papillary adenocarcinoma and undifferentiated sarcoma) in the field of prior radiation, and second, primary central nervous system tumor, a pineoblastoma.
对6例经组织学证实的视网膜母细胞瘤患者进行了计算机断层扫描检查,其中2例在初诊时检查,4例在单独接受放射治疗或联合手术治疗后的2至30年进行检查。计算机断层扫描的发现包括:视网膜肿瘤钙化、肿瘤的颅内蛛网膜下腔播散、既往放疗区域的放射性诱导肿瘤(乳头状腺癌和未分化肉瘤),以及第二原发性中枢神经系统肿瘤——松果体母细胞瘤。