Kano T, Zama A, Ono N, Nakamura T, Tamura M, Ohe T, Nakazato Y
Department of Neurosurgery, Gunma University School of Medicine.
No Shinkei Geka. 1994 Apr;22(4):367-70.
The patient was a 7-year-old boy who received radiation therapy of 50 Gy after total gross removal of a craniopharyngioma. After two years a follow up CT scan showed a new enhanced lesion in the right temporal tip within the previous irradiation field. Total removal of the tumor was performed and its histological examination showed it to be an atypical meningioma. This atypical meningioma satisfied Cahan's criteria. So we diagnosed this atypical meningioma as radiation-induced meningioma. Immunohistochemically this meningioma stained for Vimentin. An electron-microscopical examination showed neither desmosome nor interdigitation. The score of Ki-67 and BrdU-L. I. was very small. Compared with previously reported juvenile radiation-induced meningioma, the latency was very short. The patient received growth hormone (GH) replacement therapy. We suspected relation between GH replacement therapy and short latency. He was discharged without any new neurological deficits and we haven't detected tumor recurrence for two years.
该患者为一名7岁男孩,在颅咽管瘤全部肉眼切除后接受了50 Gy的放射治疗。两年后,随访CT扫描显示在先前放疗区域内的右颞尖出现一个新的强化病变。对肿瘤进行了全切,组织学检查显示为非典型脑膜瘤。该非典型脑膜瘤符合卡汉标准。因此,我们将此非典型脑膜瘤诊断为放射性诱导性脑膜瘤。免疫组化显示该脑膜瘤波形蛋白染色阳性。电子显微镜检查未发现桥粒和指状交叉。Ki-67和BrdU-L.I.评分非常低。与先前报道的青少年放射性诱导性脑膜瘤相比,潜伏期非常短。患者接受了生长激素(GH)替代治疗。我们怀疑GH替代治疗与短潜伏期之间存在关联。他出院时没有任何新的神经功能缺损,并且我们在两年内未检测到肿瘤复发。