Hodgkin & Reed-Sternberg細胞がHelper/inducer T細胞型の表面形質を示したホジキン病の1例

豊 森村, 栄子 和知, 正文 阿部, 治毅 若狭, 恵基 川上, 堅吉 北
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Abstract

We report a case of Hodgkin's disease showing helper/inducer T cell phenotype on Hodgkin & Reed-Sternberg cells.A 21 years-old Japanese female was admitted for right cervical lymphadenopathy. Laboratory tests including human T lymphocyte virus-I antibody (HTLV-I antibody) were within normal. A biopsy specimen of the cervical lymph node showed Hodgkin's disease, nodular sclerosis (NS).Immunohistologically, Hodgkin & Reed-Sternberg cells were positive for CD30 (Ki-1), CD15 (Leu-M1), CD25 (IL-2R), HLA-DR, transferrin receptor, CD2 (Leu-5b), CD3 (Leu-4), CD4 (Leu-3a), and CD5 (Leu-1), but were negative for B cell associated antigens and myeloid-monocyte associated antigens. The immunohistochemical data indicate helper/inducer T cell phenotype on Hodgkin & Reed-Sternberg cells.Southern blot analysis revealed six rearranged bands using T cell receptor gene probe (TCR Jγ1 probe), when genomic DNA of the biopsied lymph node was digested with EcoRI. Although the TCRγ gene rearrangement bands were not well evaluated, the finding of TCRγ gene rearrangement is unlikely to consider a clonal prolifaration of Hodgkin & Reed-Stenberg cells with T cell phenotype. It would be speculated in this case that rearranged bands for TCRγ may originate from functional T cell clones with transcription of the CD3 molecule and unique TCRγ rearrangements.The patient is free from the disease 2 years after the biopsy.
Hodgkin & Reed-Sternberg细胞显示Helper/inducer T细胞型表面性状的霍奇金病的一个例子
我们报告一例霍奇金病显示辅助/诱导剂T细胞表型在霍奇金和里德-斯特恩伯格细胞。一名21岁日本女性因右侧颈淋巴肿大入院。实验室检查包括人T淋巴细胞病毒i抗体(HTLV-I抗体)正常。颈部淋巴结活检显示何杰金氏病结节性硬化(NS)。免疫组织学上,霍奇金和里德-斯特恩伯格细胞CD30 (Ki-1)、CD15 (Leu-M1)、CD25 (IL-2R)、HLA-DR、转铁蛋白受体、CD2 (Leu-5b)、CD3 (Leu-4)、CD4 (Leu-3a)和CD5 (Leu-1)呈阳性,但B细胞相关抗原和骨髓单核细胞相关抗原呈阴性。免疫组织化学数据显示霍奇金和里德-斯特恩伯格细胞的辅助/诱导剂T细胞表型。用EcoRI消化活检淋巴结的基因组DNA,用T细胞受体基因探针(TCR j - γ - 1探针)进行Southern blot分析,发现6条重排条带。虽然TCRγ基因重排带没有得到很好的评估,但TCRγ基因重排的发现不太可能考虑具有T细胞表型的霍奇金和里德-斯坦伯格细胞的克隆增殖。在这种情况下,我们可以推测TCRγ重排的条带可能来自具有CD3分子转录和独特TCRγ重排的功能性T细胞克隆。患者在活检后2年不再患病。
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