Department of Medicine and Clinical Science, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Int J Hematol. 2012 Jan;95(1):77-85. doi: 10.1007/s12185-011-0986-5. Epub 2011 Dec 23.
T-cell prolymphocytic leukemia (T-PLL) is a rare type of peripheral T-cell leukemia. In this study, we examined the clinical and biological characteristics of 11 Japanese patients with T-PLL. Median age was 74 years, with male predominance. Median lymphocyte frequency was 85.3% in blood. Physical characteristics were splenomegaly (36.4%), tiny lymph adenopathy (63.6%), skin lesion (9.1%) and pleural effusion (27.3%). Median survival was 30.1 months, despite treatment with various chemotherapeutic modalities. Although complex chromosomal abnormalities were observed in 5 of 11 cases (45.5%), typical 14q32 and Xq28 abnormalities were not detected. TCL1A mRNA expression was observed in 6 of 11 cases (54.5%) on real-time quantitative PCR. In 5 of these 6 cases, flow cytometric analysis and/or immunohistochemistry confirmed the expression of TCLA1 protein. Split signals for the TCL1 region on fluorescence in situ hybridization confirmed rearrangement in 3 out of 7 cases evaluated. These cases corresponded to cases that were positive for TCL1A expression, suggesting that rearrangement of the TCL1 region induced high expression of TCL1A gene. In summary, a substantial number of T-PLL cases in Japan had abnormal expression of TCL1A, probably due to rearrangement of TCL1 region. Expression and/or rearrangement of TCL1A may, therefore, be a useful marker for diagnosing T-PLL, regardless of chromosomal abnormalities.
T 细胞前淋巴细胞白血病(T-PLL)是一种罕见的外周 T 细胞白血病。在这项研究中,我们检查了 11 例日本 T-PLL 患者的临床和生物学特征。中位年龄为 74 岁,男性居多。血液中淋巴细胞频率的中位数为 85.3%。体格特征包括脾肿大(36.4%)、小结节性淋巴结病(63.6%)、皮肤病变(9.1%)和胸腔积液(27.3%)。尽管采用了各种化疗方式,但中位生存时间仅为 30.1 个月。尽管在 11 例中有 5 例(45.5%)观察到复杂的染色体异常,但未检测到典型的 14q32 和 Xq28 异常。在实时定量 PCR 中,在 11 例中有 6 例(54.5%)观察到 TCL1A mRNA 的表达。在这 6 例中的 5 例中,通过流式细胞术分析和/或免疫组织化学证实了 TCLA1 蛋白的表达。在 7 例中评估的荧光原位杂交的 TCL1 区域的分裂信号证实了重排。这些病例与 TCL1A 表达阳性的病例相对应,表明 TCL1 区域的重排诱导了 TCL1A 基因的高表达。总之,日本的大量 T-PLL 病例存在 TCL1A 的异常表达,可能是由于 TCL1 区域的重排。因此,TCL1A 的表达和/或重排可能是诊断 T-PLL 的有用标志物,而与染色体异常无关。