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儿童髓母细胞瘤:根治性切除及低剂量全脑脊髓放疗的结果

Medulloblastoma in childhood: results of radical resection and low-dose neuraxis radiation therapy.

作者信息

Tomita T, McLone D G

出版信息

J Neurosurg. 1986 Feb;64(2):238-42. doi: 10.3171/jns.1986.64.2.0238.

DOI:10.3171/jns.1986.64.2.0238
PMID:3944633
Abstract

This review concerns 22 children who were treated from 1980 through 1983 for medulloblastoma in the posterior fossa. Treatment included attempts at radical resection of the tumor and postoperative craniospinal radiation therapy, with 5000 to 5500 rads directed to the posterior fossa and 2500 rads to the remaining craniospinal axis. This lower radiation dose to the neuraxis was used to avoid late adverse effects upon the growing central nervous system of the children. Gross confirmation of total resection was obtained in 13 patients (the "total resection group"); however, nine patients had a subtotal resection leaving a small portion of the tumor extending into the cerebellar peduncles or the cerebellopontine angle, or else encasing the posterior inferior cerebellar artery (the "subtotal resection group"). Six patients in the total resection group demonstrated tumor extension into the cerebellar peduncles, which was removed by means of a surgical carbon dioxide laser without neurological sequelae. Biopsy of the arachnoid membrane from the cisterna magna and cytological examination of the cerebrospinal fluid (CSF) prior to manipulation of the tumor were carried out in 12 patients. All but one showed dissemination of medulloblastoma cells. Myelography and CSF cytological study were undertaken 2 months after radiation therapy in 12 patients and were positive in two. There were no case mortalities in the total resection group during the 24- to 67-month follow-up period, whereas the 1-year survival rate in the "subtotal resection group" was only 44.4%. This study suggests that medulloblastoma can be controlled with a low radiation dose to the neuraxis, should a grossly confirmed total resection be achieved at craniotomy.

摘要

本综述涉及1980年至1983年期间接受治疗的22例后颅窝髓母细胞瘤患儿。治疗方法包括尝试根治性切除肿瘤以及术后颅脊髓放射治疗,后颅窝接受5000至5500拉德的照射,其余颅脊髓轴接受2500拉德的照射。对神经轴采用较低的放射剂量是为了避免对儿童生长中的中枢神经系统产生晚期不良影响。13例患者(“全切组”)获得了肿瘤全切的大体确认;然而,9例患者为次全切除,残留一小部分肿瘤延伸至小脑脚或桥小脑角,或者包绕小脑后下动脉(“次全切组”)。全切组中有6例患者的肿瘤延伸至小脑脚,通过手术二氧化碳激光切除,未出现神经后遗症。12例患者在处理肿瘤前对枕大池蛛网膜进行了活检并对脑脊液(CSF)进行了细胞学检查。除1例患者外,其余均显示有髓母细胞瘤细胞播散。12例患者在放射治疗后2个月进行了脊髓造影和脑脊液细胞学检查,2例结果呈阳性。在24至67个月的随访期内,全切组无病例死亡,而“次全切组”的1年生存率仅为44.4%。本研究表明,如果在开颅手术时实现了大体确认的肿瘤全切,髓母细胞瘤可以通过对神经轴采用低放射剂量来控制。

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