Bown N, Reid M M, Pearson A D, Davison E V, Malcolm A J, Craft A W
Department of Human Genetics, University of Newcastle upon Tyne.
J Clin Pathol. 1987 Nov;40(11):1334-6. doi: 10.1136/jcp.40.11.1334.
In a patient with stage IV disseminated neuroblastoma treated by chemotherapy extensive cytogenetic investigations were performed on the residual primary tumour and bone marrow immediately before myeloablative treatment and autologous marrow rescue. Two abnormal clones both showing lp+, a characteristic abnormality of neuroblastoma, were detected in cells from the residual primary tumour, providing direct evidence of persisting viable tumour. Such investigations should be a routine part of the assessment of response to treatment in patients with neuroblastoma, and could be extended to others in whom "second look" surgery is performed.
在一名接受化疗的IV期播散性神经母细胞瘤患者中,在进行清髓性治疗和自体骨髓挽救之前,对残留的原发肿瘤和骨髓进行了广泛的细胞遗传学研究。在残留原发肿瘤的细胞中检测到两个均显示1p+的异常克隆,这是神经母细胞瘤的特征性异常,为持续存在的存活肿瘤提供了直接证据。此类研究应成为神经母细胞瘤患者治疗反应评估的常规部分,并且可以扩展到进行“二次探查”手术的其他患者。