Furuta T, Tabuchi A, Adachi Y, Mizumatsu S, Tamesa N, Ichikawa T, Tamiya T, Matsumoto K, Ohmoto T
Department of Neurological Surgery, Okayama University Medical School, Japan.
Brain Tumor Pathol. 1998;15(1):7-12. doi: 10.1007/BF02482094.
During the period from 1966 to 1996 the authors analyzed the clinicopathological characteristics of 46 cases of histologically verified primary brain tumors with symptomatic onset during the first 3 years of life. The patient group included 27 males and 19 females. There were 14 patients during the first year, 13 during the second year, and 19 during the third year. Supratentorial tumors (60.9%) were more common than infratentorial tumors. Histologically, neuroepithelial tumors predominated. The incidence of ependymal tumors, particularly malignant ones, and of neuronal/mixed neuronal-glial tumors was higher than in previous reports. Congenital brain tumors, those occurring within 2 months after birth, or tumors of dysplastic origin comprised 42.9% of the tumors that developed within 1 year of birth. At the onset, macrocephaly, failure to thrive, and seizures were prominent symptoms or signs in the younger patients. Focal neurological deficits and increased intracranial pressure predominated in the older patients. All but one patient underwent surgical treatment, and 17 patients received adjuvant therapy after surgery. The prognosis was mainly related to the histology of the malignancy. The outcome of medulloblastomas was poor. The quality of life of surviving patients was relatively good, 77.8% having better performance status (PS) than the Eastern Cooperative Oncology Group PS 2.
在1966年至1996年期间,作者分析了46例经组织学证实的原发性脑肿瘤的临床病理特征,这些肿瘤在生命的前3年出现症状。患者组包括27名男性和19名女性。第一年有14例患者,第二年有13例,第三年有19例。幕上肿瘤(60.9%)比幕下肿瘤更常见。从组织学上看,神经上皮肿瘤占主导地位。室管膜瘤,尤其是恶性室管膜瘤以及神经元/混合性神经元-胶质细胞瘤的发生率高于以往报道。先天性脑肿瘤,即出生后2个月内发生的肿瘤,或发育异常起源的肿瘤占出生后1年内发生的肿瘤的42.9%。发病时,头大、发育不良和癫痫是较年轻患者的突出症状或体征。年长患者以局灶性神经功能缺损和颅内压升高为主。除1例患者外,所有患者均接受了手术治疗,17例患者术后接受了辅助治疗。预后主要与恶性肿瘤的组织学有关。髓母细胞瘤的预后较差。存活患者的生活质量相对较好,77.8%的患者表现状态(PS)优于东部肿瘤协作组的PS 2。