Fisher P G, Breiter S N, Carson B S, Wharam M D, Williams J A, Weingart J D, Foer D R, Goldthwaite P T, Tihan T, Burger P C
Department of Neurology, Stanford University School of Medicine, Palo Alto, California 94305-5235, USA.
Cancer. 2000 Oct 1;89(7):1569-76. doi: 10.1002/1097-0142(20001001)89:7<1569::aid-cncr22>3.0.co;2-0.
Brain stem tumors in children have been classified pathologically as low grade or high grade gliomas and descriptively as diffuse gliomas, intrinsic gliomas, midbrain tumors, tectal gliomas, pencil gliomas, dorsal exophytic brain stem tumors, pontine gliomas, focal medullary tumors, cervicomedullary tumors, focal gliomas, or cystic gliomas.
To search for a simplified and prognostic clinicopathologic scheme for brain stem tumors, the authors reviewed a consecutive cohort of patients younger than age 21 years with tumors diagnosed from 1980 through 1997. Pathology specimens and neuroimaging were classified by masked review. Statistical and survival analysis along with Cox proportional hazards regression was performed.
Seventy-six patients were identified, with initial diagnostic magnetic resonance imaging available for 51 and pathology specimens for 48 patients. Twenty cases were classified histologically as pilocytic astrocytoma (PA), 14 as fibrillary astrocytoma (FA), and 14 as other tumors or indeterminate pathology. For all tumors, characteristics significantly associated with a worse survival rate were: symptom duration less than 6 months before diagnosis (P = 0.004); abducens palsy at presentation (P < 0.0001); pontine location (P = 0.0002); and engulfment of the basilar artery (P = 0.006). Pilocytic astrocytoma was associated with location outside the ventral pons (P = 0.001) and dorsal exophytic growth (P = 0.013); Fibrillary astrocytoma was associated with symptoms less than 6 months (P = 0. 006), abducens palsy (P < 0.001), and engulfment of the basilar artery (P = 0.002). Pilocytic astrocytoma showed 5-year overall survival (OS) of 95% (standard error [SE], 5%) compared with FA 1-year OS of 23% (SE, 11%;P < 0.0001).
Brain stem tumors can be succinctly and better biologically classified as diffusely infiltrative brain stem gliomas-generally FA located in the ventral pons that present with abducens palsy, often engulf the basilar artery, and carry a grim prognosis-and focal brain stem gliomas-frequently PA arising outside the ventral pons, often with dorsal exophytic growth, a long clinical prodrome, and outstanding prognosis for survival. Our findings emphasize the individuality of PA as a distinct clinicopathologic entity with an exceptional prognosis.
儿童脑干肿瘤在病理上被分类为低级别或高级别胶质瘤,在描述上被分类为弥漫性胶质瘤、原发性胶质瘤、中脑肿瘤、顶盖胶质瘤、铅笔状胶质瘤、背侧外生性脑干肿瘤、脑桥胶质瘤、局灶性延髓肿瘤、颈髓肿瘤、局灶性胶质瘤或囊性胶质瘤。
为了寻找一种简化的、具有预后价值的脑干肿瘤临床病理方案,作者回顾了1980年至1997年期间诊断的连续队列的21岁以下肿瘤患者。病理标本和神经影像学通过盲法评估进行分类。进行了统计和生存分析以及Cox比例风险回归分析。
共确定76例患者,51例有初始诊断性磁共振成像,48例有病理标本。20例组织学分类为毛细胞型星形细胞瘤(PA),14例为纤维型星形细胞瘤(FA),14例为其他肿瘤或病理诊断不明确。对于所有肿瘤,与较差生存率显著相关的特征为:诊断前症状持续时间少于6个月(P = 0.004);就诊时展神经麻痹(P < 0.0001);脑桥部位(P = 0.0002);以及基底动脉包绕(P = 0.006)。毛细胞型星形细胞瘤与脑桥腹侧以外的部位相关(P = 0.001)和背侧外生性生长相关(P = 0.013);纤维型星形细胞瘤与症状持续时间少于6个月(P = 0.006)、展神经麻痹(P < 0.001)和基底动脉包绕相关(P = 0.002)。毛细胞型星形细胞瘤的5年总生存率(OS)为95%(标准误[SE],5%),而纤维型星形细胞瘤的1年总生存率为23%(SE,11%;P < 0.0001)。
脑干肿瘤可以简洁地、在生物学上更好地分类为弥漫性浸润性脑干胶质瘤——通常是位于脑桥腹侧的纤维型星形细胞瘤,表现为展神经麻痹,常包绕基底动脉,预后不良——以及局灶性脑干胶质瘤——通常是起源于脑桥腹侧以外的毛细胞型星形细胞瘤,常伴有背侧外生性生长,临床前期较长,生存预后良好。我们的研究结果强调了毛细胞型星形细胞瘤作为一种具有特殊预后的独特临床病理实体的个体性。