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儿童低级别星形细胞瘤间变的发展

Development of anaplastic changes in low-grade astrocytomas of childhood.

作者信息

Dirks P B, Jay V, Becker L E, Drake J M, Humphreys R P, Hoffman H J, Rutka J T

机构信息

Division of Neurosurgery, Hospital for Sick Children, University of Toronto, Ontario, Canada.

出版信息

Neurosurgery. 1994 Jan;34(1):68-78.

PMID:8121571
Abstract

The authors present their experience with six children who developed anaplastic astrocytomas after receiving treatment for low-grade astrocytomas. Five children were from a series of 55 children with optic chiasmatic-hypothalamic gliomas who have been studied since 1976. The sixth child initially had a low-grade astrocytoma of the thalamus. The mean age of the children at initial presentation was 5.3 years. Five children were treated with surgery and radiation therapy; one child with a chiasmatic-hypothalamic glioma received radiation therapy alone. The amount of external radiation therapy used in all children was 50-52.5 Gy delivered in standard fractionations over approximately 6 weeks to include the volume of the original tumor plus a margin of 2 cm. The time to anaplastic transformation varied between 2 and 10 years (mean, 6.4 years). At tumor recurrence, the children had seizures or symptoms and signs of raised intracranial pressure. The location of the second tumor in all patients was either at the primary site or within the field of radiation therapy. Five of the six children underwent a second craniotomy and subtotal resection of their malignant gliomas. One child had positive cerebrospinal fluid cytology and multiple intraspinal metastatic tumor nodules detected by magnetic resonance imaging. On histopathological examination, four children had anaplastic astrocytoma, and two had glioblastoma multiforme. Four of the six children have died of their anaplastic astrocytomas (mean time from diagnosis of anaplastic astrocytoma to death, 10 months). Two children underwent chemotherapy and spinal irradiation for their anaplastic astrocytomas, and are currently alive and undergoing treatment. The possible mechanisms by which anaplastic tumors have developed in children treated previously for low-grade astrocytomas is discussed. The data suggest that radiation therapy may have played an integral role in the genesis of anaplastic astrocytomas in these children.

摘要

作者介绍了6例儿童在接受低级别星形细胞瘤治疗后发生间变性星形细胞瘤的经验。其中5例儿童来自自1976年以来一直在研究的55例视交叉 - 下丘脑胶质瘤患儿系列。第6例儿童最初患有丘脑低级别星形细胞瘤。这些儿童初次就诊时的平均年龄为5.3岁。5例儿童接受了手术和放射治疗;1例视交叉 - 下丘脑胶质瘤患儿仅接受了放射治疗。所有儿童使用的外照射剂量为50 - 52.5 Gy,在约6周内以标准分割方式给予,照射范围包括原肿瘤体积加上2 cm的边缘。间变性转化的时间在2至10年之间(平均6.4年)。肿瘤复发时,儿童出现癫痫发作或颅内压升高的症状和体征。所有患者的第二个肿瘤位置要么在原发部位,要么在放射治疗野内。6例儿童中有5例接受了第二次开颅手术并次全切除了恶性胶质瘤。1例儿童脑脊液细胞学检查呈阳性,磁共振成像检测到多个脊髓转移瘤结节。组织病理学检查显示,4例儿童为间变性星形细胞瘤,2例为多形性胶质母细胞瘤。6例儿童中有4例死于间变性星形细胞瘤(从间变性星形细胞瘤诊断到死亡的平均时间为10个月)。2例儿童因间变性星形细胞瘤接受了化疗和脊髓照射,目前尚存活并正在接受治疗。本文讨论了先前接受低级别星形细胞瘤治疗的儿童发生间变性肿瘤的可能机制。数据表明,放射治疗可能在这些儿童间变性星形细胞瘤的发生中起到了重要作用。

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