Matsumoto Masato, Horiuchi Kazuomi, Sato Taku, Oinuma Masahiro, Sakuma Jun, Suzuki Kyouichi, Sasaki Tatsuya, Kodama Namio, Watanabe Kazuo, Suzuki Toshimitsu
Department of Neurosurgery, Fukushima Medical University, Japan.
Neurol Med Chir (Tokyo). 2007 Sep;47(9):428-33. doi: 10.2176/nmc.47.428.
An 8-year-old boy presented with a rare cerebral medulloepithelioma manifesting as headache, nausea, and vomiting. Neuroimaging demonstrated a mass containing a cyst in the left frontal lobe. Gross total resection of the tumor with a 1-cm margin was performed under intraoperative monitoring. The histological diagnosis was medulloepithelioma. Stereotactic radiotherapy (total dose 20 Gy) was given to the brain up to 1 cm from the surgical margin. Follow-up neuroimaging 5 years later showed no signs of recurrence. He now attends junior high school, with normal mental and physiological development. Medulloepitheliomas are rare, highly malignant embryonal tumors of the central nervous system. Combined gross total tumor resection and radiotherapy are recommended to obtain the most favorable outcome.
一名8岁男孩因罕见的脑髓上皮瘤就诊,表现为头痛、恶心和呕吐。神经影像学检查显示左额叶有一个含囊肿的肿块。在术中监测下对肿瘤进行了全切,切缘为1厘米。组织学诊断为髓上皮瘤。对手术切缘外1厘米范围内的脑部进行了立体定向放射治疗(总剂量20 Gy)。5年后的随访神经影像学检查未显示复发迹象。他现在上初中,心理和生理发育正常。髓上皮瘤是中枢神经系统罕见的高度恶性胚胎性肿瘤。建议联合肿瘤全切和放射治疗以获得最有利的结果。