Tanahashi Takahiro, Sekiguchi Nodoka, Matsuda Kazuyuki, Takezawa Yuka, Ito Toshiro, Kobayashi Hikaru, Ichikawa Naoaki, Nishina Sayaka, Senoo Noriko, Sakai Hitoshi, Nakazawa Hideyuki, Ishida Fumihiro
Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan.
Division of Hematology, Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan; Department of Comprehensive Cancer Therapy, Shinshu University School of Medicine, Matsumoto, Japan.
Leuk Res. 2016 Jun;45:8-13. doi: 10.1016/j.leukres.2016.04.001. Epub 2016 Apr 4.
Large granular lymphocyte leukemia (LGL-L) has been morphologically defined as a group of lymphoproliferative disorders, including T-cell large granular lymphocytic leukemia (T-LGL-L), chronic lymphoproliferative disorders of NK cells (CLPD-NK) and aggressive NK cell leukemia. We investigated the morphological features of LGL leukemic cells in 26 LGL-L patients in order to elucidate relationships with current classifications and molecular backgrounds. LGL-L cells were mostly indistinguishable from normal LGL. Patients with STAT3 SH2 domain mutations showed significantly smaller cells compared with patients without STAT3 mutations. Four patients with T-LGL-L showed smaller granular lymphocytes with a median diameter of less than 13μm, which were rarely seen in normal subjects. This small subtype of T-LGL-L was recognized among rather young patients and was associated with D661Y mutations in the STAT3 gene SH2 domain. In addition, all of them showed anemia including two cases with pure red cell aplasia. These results suggest the heterogeneity of T-LGL-L and a specific subtype with small variants of T-LGL-L.
大颗粒淋巴细胞白血病(LGL-L)在形态学上被定义为一组淋巴增殖性疾病,包括T细胞大颗粒淋巴细胞白血病(T-LGL-L)、NK细胞慢性淋巴增殖性疾病(CLPD-NK)和侵袭性NK细胞白血病。我们研究了26例LGL-L患者中LGL白血病细胞的形态学特征,以阐明其与当前分类和分子背景的关系。LGL-L细胞大多与正常LGL难以区分。与无STAT3突变的患者相比,有STAT3 SH2结构域突变的患者细胞明显更小。4例T-LGL-L患者的颗粒淋巴细胞较小,中位直径小于13μm,这在正常受试者中很少见。这种T-LGL-L的小细胞亚型在相当年轻的患者中被识别出来,并且与STAT3基因SH2结构域中的D661Y突变相关。此外,他们均表现出贫血,其中2例为纯红细胞再生障碍。这些结果提示了T-LGL-L的异质性以及T-LGL-L小细胞变体的一种特定亚型。