Macera M J, DiPillo F, Szabo P, Ramirez R, Gogineni S, Verma R S
Department of Medicine, Long Island College Hospital, SUNY, New York.
Leukemia. 1994 Mar;8(3):420-4.
Human T-lymphotropic virus type I (HTLV-1) integration has been associated with the development of adult T-cell leukemia/lymphoma (ATL). Recently, a correlation between T-cell receptor (TCR) gene rearrangements and chromosomal aberrations has been implicated in this leukemia. We present a case of HTLV-1 infected adult T-cell lymphoma that initially presented with a normal karyotype and germline J beta I/J beta II loci. As the disease evolved to the aggressive stage, a complex chromosomal rearrangement with a duplication of chromosome 6p23-->pter translocated to a derivative chromosome 16, was identified by molecular cytogenetic techniques. The nature of this complex abnormality would have been difficult to determine if only conventional banding techniques were performed. Rearrangement involving one J beta allele was also detected at that time. After initiation of chemotherapy, no germline J beta loci were detected, suggesting a possible second rearrangement involving this locus that was homologous. Although no known immune response genes are located at the breakpoints involved in this abnormality, the chromosomal aberration concurred with the initial J beta rearrangement.
人类嗜T淋巴细胞病毒I型(HTLV-1)整合与成人T细胞白血病/淋巴瘤(ATL)的发生有关。最近,T细胞受体(TCR)基因重排与染色体畸变之间的相关性被认为与这种白血病有关。我们报告一例HTLV-1感染的成人T细胞淋巴瘤病例,该病例最初表现为正常核型和种系JβI/JβII基因座。随着疾病发展到侵袭性阶段,通过分子细胞遗传学技术鉴定出一种复杂的染色体重排,即6号染色体p23→pter重复并易位至衍生的16号染色体。如果仅采用传统的显带技术,这种复杂异常的性质将很难确定。当时还检测到涉及一个Jβ等位基因的重排。化疗开始后,未检测到种系Jβ基因座,提示可能存在涉及该基因座的第二次同源重排。尽管在这种异常所涉及的断点处未发现已知的免疫反应基因,但染色体畸变与最初的Jβ重排同时出现。