T细胞受体
淋巴细胞增多症
T淋巴细胞
断点
染色体异常
医学
基因重排
异常
基因
淋巴细胞
核型
生物
T细胞
染色体易位
病理
免疫学
遗传学
染色体
抗原
免疫系统
精神科
作者
K. F. Wong,J. Chan,H. S. Y. Liu,C. Man,Yok‐Lam Kwong
标识
DOI:10.1046/j.0007-1048.2001.03315.x
摘要
Summary. Cytogenetic information on T‐cell large granular lymphocyte leukaemia (T‐LGL; large granular lymphocytosis) is limited. We report two cases of T‐LGL with unusual karyotypic aberrations. The first case showed a novel inv(7)(p15q22) as the sole chromosomal abnormality, while the second case showed an inv(14)(q11q32) with evidence of clonal evolution. The breakpoints 7p14–p15 and 14q11 coincide with the T‐cell receptor (TCR)‐γ and TCR‐α/TCR‐δ gene loci respectively. This is the first report describing the possible involvement of T‐cell receptor genes in karyotypic aberrations in T‐LGL.
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