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儿童间脑胶质瘤。一项临床病理研究。

Diencephalic gliomas of children. A clinicopathologic study.

作者信息

Albright A L, Price R A, Guthkelch A N

出版信息

Cancer. 1985 Jun 15;55(12):2789-93. doi: 10.1002/1097-0142(19850615)55:12<2789::aid-cncr2820551212>3.0.co;2-a.

Abstract

The authors reviewed the clinical information and pathology specimens from 29 children with diencephalic gliomas to determine whether any clinical or histopathologic feature correlated with prognosis. The median survival time for the entire group was 3.96 years. No symptom or sign at the time of diagnosis correlated with outcome. The tumors consisted of 25 astrocytomas or mixed gliomas and 4 malignant astrocytomas-mixed gliomas. Median survival time of the 25 children with astrocytomas-mixed gliomas was 4.8 years, compared with 0.5 years for the 4 children with malignant tumors. The tumor histology was relatively uniform: most tumors were moderately cellular astrocytomas with pleomorphism and hyperchromatism but without mitoses, hemorrhage, or necrosis. High cell density and the presence of mitoses were the two histologic features significantly associated with poor prognosis; no child with mitosis survived longer than 14 months.

摘要

作者回顾了29例间脑胶质瘤患儿的临床信息和病理标本,以确定是否有任何临床或组织病理学特征与预后相关。整个组的中位生存时间为3.96年。诊断时的任何症状或体征均与预后无关。肿瘤包括25例星形细胞瘤或混合性胶质瘤以及4例恶性星形细胞瘤-混合性胶质瘤。25例星形细胞瘤-混合性胶质瘤患儿的中位生存时间为4.8年,而4例患有恶性肿瘤的患儿的中位生存时间为0.5年。肿瘤组织学相对一致:大多数肿瘤为中度细胞性星形细胞瘤,具有多形性和核深染,但无有丝分裂、出血或坏死。高细胞密度和有丝分裂的存在是与预后不良显著相关的两个组织学特征;有丝分裂的患儿无一人存活超过14个月。

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