Garcia-Sanchez F, Menárguez J, Cristobal E, Cantalejo A, Gil J, Algara P, Vicario J L
Regional Transfusion Centre, Madrid, Spain.
Br J Haematol. 1995 Aug;90(4):943-6. doi: 10.1111/j.1365-2141.1995.tb05221.x.
We report the first case of T-cell gamma delta+ hepatosplenic malignant lymphoma in childhood. Tumour-specific oligoprobes were developed against the single V1-J1 rearrangement of the delta T-cell receptor (TCR) gene in order to perform minimal residual disease (MRD) studies. Molecular analysis in serial bone marrow samples proved to be of predictive value concerning the clinical outcome. Clonotypic DNA was not detected in peripheral blood during the course of the disease until a refractory terminal leukaemic phase took place 18 months after the diagnosis. This case demonstrates the usefulness of MRD studies to monitor the course of disease in at least some subsets of peripheral T-cell lymphomas.
我们报告了首例儿童T细胞γδ+肝脾恶性淋巴瘤病例。针对δT细胞受体(TCR)基因的单一V1-J1重排开发了肿瘤特异性寡核苷酸探针,以进行微小残留病(MRD)研究。对系列骨髓样本的分子分析被证明对临床结果具有预测价值。在疾病过程中,外周血中未检测到克隆型DNA,直到诊断后18个月进入难治性终末期白血病阶段。该病例证明了MRD研究在监测至少某些外周T细胞淋巴瘤亚组疾病进程中的有用性。