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儿童髓母细胞瘤的骨转移;与流式细胞术DNA分析的相关性

Bone metastases of medulloblastoma in childhood; correlation with flow cytometric DNA analysis.

作者信息

Tomita T, Das L, Radkowski M A

机构信息

Division of Pediatric Neurosurgery, Children's Memorial Hospital, Chicago, Illinois.

出版信息

J Neurooncol. 1990 Apr;8(2):113-20. doi: 10.1007/BF00177833.

DOI:10.1007/BF00177833
PMID:2358845
Abstract

Thirty children with medulloblastoma who were treated between 1980 and 1986 are presented. Flow cytometric DNA analysis using formalin-fixed and paraffin-embedded tissues showed that 15 were DNA aneuploid, 13 diploid and 2 tetraploid. After homogeneous treatment with a combination of radical resection and radiation therapy, patients with DNA aneuploid medulloblastoma showed significantly better outcome (p = 0.003). Among these 30 patients, 6 (20%) had bone metastases of medulloblastoma during a minimum of 2-year follow-up period. DNA ploidy of these patients was diploid in 5 and aneuploid in 1. Incidence of bone metastases appears to correlate with DNA ploidy (p = 0.046). At the time of discovery of bone metastases, 4 had no demonstrable recurrence in the central nervous system (CNS). Radionuclide bone scan was more sensitive in disclosing these lesions, while only one patient had positive results of bone marrow aspirates/biopsy. Three patients were treated with chemotherapy, two had a combination of regional irradiation and chemotherapy and one refused treatment. All treated bone metastases in 5 patients responded clinically and radiographically, but only one patient is alive 66 months after therapy. Four patients died due to either CNS recurrence of septic complication of chemotherapy. Early detection of bone metastases by use of frequent bone scans is important. Patients with diploid medulloblastoma should be treated with adjuvant chemotherapy in order to prevent recurrences and metastases.

摘要

本文报告了1980年至1986年间接受治疗的30例髓母细胞瘤患儿。使用福尔马林固定和石蜡包埋组织进行的流式细胞术DNA分析显示,15例为DNA非整倍体,13例为二倍体,2例为四倍体。在接受根治性切除和放射治疗联合的同质治疗后,DNA非整倍体髓母细胞瘤患者的预后明显更好(p = 0.003)。在这30例患者中,6例(20%)在至少2年的随访期内发生了髓母细胞瘤骨转移。这些患者的DNA倍体中,5例为二倍体,1例为非整倍体。骨转移的发生率似乎与DNA倍体相关(p = 0.046)。在发现骨转移时,4例中枢神经系统(CNS)无明显复发。放射性核素骨扫描在发现这些病变方面更敏感,而只有1例患者骨髓穿刺/活检结果为阳性。3例患者接受了化疗,2例接受了局部放疗和化疗联合治疗,1例拒绝治疗。5例接受治疗的骨转移患者在临床和影像学上均有反应,但治疗后66个月只有1例患者存活。4例患者死于CNS复发或化疗的败血症并发症。通过频繁进行骨扫描早期发现骨转移很重要。二倍体髓母细胞瘤患者应接受辅助化疗以预防复发和转移。

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