Ichinohasama R, Endoh K, Ishizawa K, Okuda M, Kameoka J, Meguro K, Myers J, Kadin M E, Mori S, Sawai T
Department of Pathology, Tohoku University Hospital, Sendai, Japan.
Cancer. 1996 Jun 15;77(12):2592-603. doi: 10.1002/(SICI)1097-0142(19960615)77:12<2592::AID-CNCR25>3.0.CO;2-M.
Recently, it was demonstrated that the human fetal thymocyte contains a bipotential progenitor capable of both T lymphocyte and natural killer (NK) cell differentiation. However, prior to this report a malignant neoplasm arising from these cells had not been documented.
A Japanese female age 38 years was examined by morphology of light and electron microscopy, immunohistochemistry, 3-color flow cytometry, cytotoxic assay, and Southern blotting.
The patient presented with a mediastinal mass and pleural effusion. Leukemic progression was identified following chemotherapy and complete clinical remission. Immunophenotyping of lymphoma revealed CD45++, c-kit dim+, terminal deoxynucleotidyl transferase (TdT)-<+, CD38++, CD34+<++, CD33+<-, CD13dim+approximately+, HLA-DR+, CD7+, cytoplasmic CD3 (cCD3)+, surface CD3 (sCD3)-, CD2dim+, CD56+, CD16-, CD11b+, CD57-, CD1a-, CD5-, TCR alpha beta-, TCR gamma delta-, CD4-, CD8-, CD28-, CD10-, CD19-, CD20-, CD22-, surface immunoglobulins-, and CD14-. Functional NK activity of the lymphoma cells was extremely low. DNA analysis revealed no gene rearrangement in TCR beta, gamma, and delta or immunoglobulin heavy and light chain genes.
Lymphoma cells of this case were derived from a distinct subtype of lymphocyte that originate from a thymic precursor committed to NK cell differentiation. This category is different from those of thymic T or precursor B cell pheno-/genotype.
最近有研究表明,人类胎儿胸腺细胞含有一种双能祖细胞,能够分化为T淋巴细胞和自然杀伤(NK)细胞。然而,在该报告之前,尚未有文献记载由这些细胞产生的恶性肿瘤。
对一名38岁的日本女性进行了光镜和电镜形态学、免疫组织化学、三色流式细胞术、细胞毒性测定和Southern印迹分析。
该患者表现为纵隔肿块和胸腔积液。化疗后出现白血病进展,随后达到完全临床缓解。淋巴瘤的免疫表型分析显示CD45++、c-kit dim+、末端脱氧核苷酸转移酶(TdT)-<+、CD38++、CD34+<++、CD33+< -、CD13dim+约+、HLA-DR+、CD7+、胞质CD3(cCD3)+、表面CD3(sCD3)-、CD2dim+、CD56+、CD16-、CD11b+、CD57-、CD1a-、CD5-、TCRαβ-、TCRγδ-、CD4-、CD8-、CD28-、CD10-、CD19-、CD20-、CD22-、表面免疫球蛋白-和CD14-。淋巴瘤细胞的功能性NK活性极低。DNA分析显示TCRβ、γ和δ或免疫球蛋白重链和轻链基因无基因重排。
该病例的淋巴瘤细胞来源于一种独特的淋巴细胞亚型,起源于致力于NK细胞分化的胸腺前体细胞。这一类别与胸腺T或前体B细胞表型/基因型不同。