Win Khin Than, Hsieh Yen-Chuan, Yang Chun-Chieh, Chang Sheng-Tsung, Su Ying-Zhen, Tien Hwei-Fang, Chuang Shih-Sung
Department of Pathology, Chi-Mei Medical Center, Tainan, Taiwan.
Department of Intensive Care Medicine, Chi-Mei Medical Center, Tainan, Taiwan.
Anal Quant Cytopathol Histpathol. 2013 Aug;35(4):232-6.
Large granular lymphocytes (LGLs) are either cytotoxic T or natural killer (NK) cells exhibiting round nuclei and azurophilic cytoplasmic granules. Morphologically, neoplastic LGLs of T cell lineage (T-LGLLs) are usually indistinguishable from normal LGLs, while there is a wide morphological range of aggressive NK cell leukemia (ANKL).
We present 2 consecutive cases of leukemia comprising pleomorphic LGLs. One patient presented with drowsy consciousness and unstable hemodynamics. Her peripheral blood smear disclosed a significant number of LGLs with pleomorphic nuclei expressing CD2, CD56 and HLA-DR but not surface or cytoplasmic CD3 (cCD3). The second patient, previously healthy, presented with a sudden death. Her peripheral blood revealed LGLs ranging from round to pleomorphic nuclei with a CD2+ cCD3+ surface CD3- CD56+ phenotype and clonally rearranged T cell receptor gene. The findings of the first patient were consistent with ANKL and the second, T-LGLL. Both patients passed away shortly before treatment.
The 2 cases highlight the importance of a multidisciplinary approach in addition to cytological examination to reach accurate diagnoses of such rare leukemia cases.
大颗粒淋巴细胞(LGL)是具有圆形细胞核和嗜天青细胞质颗粒的细胞毒性T细胞或自然杀伤(NK)细胞。在形态学上,T细胞系的肿瘤性大颗粒淋巴细胞(T-LGLL)通常与正常LGL难以区分,而侵袭性NK细胞白血病(ANKL)的形态学范围则很广。
我们报告2例连续性白血病病例,其特征为多形性大颗粒淋巴细胞。1例患者表现为意识模糊和血流动力学不稳定。其外周血涂片显示大量具有多形性细胞核的大颗粒淋巴细胞,表达CD2、CD56和HLA-DR,但不表达表面或细胞质CD3(cCD3)。第2例患者既往健康,突然死亡。其外周血显示大颗粒淋巴细胞细胞核从圆形到多形性不等,具有CD2+cCD3+、表面CD3-、CD56+表型以及克隆性重排的T细胞受体基因。第1例患者的检查结果符合ANKL,第2例符合T-LGLL。2例患者均在治疗前不久死亡。
这2例病例凸显了除细胞学检查外多学科方法对于准确诊断此类罕见白血病病例的重要性。