Bakels V, van Oostveen J W, van der Putte S C, Meijer C J, Willemze R
Department of Dermatology, Free University Hospital, Amsterdam, The Netherlands.
Am J Pathol. 1997 Jun;150(6):1941-9.
Differentiation between cutaneous pseudo-T-cell lymphomas and cutaneous T-cell lymphomas (CTCLs) may be extremely difficult. In this study, it was investigated whether demonstration of an aberrant phenotype and detection of clonal T-cell receptor gamma (TCR gamma) gene rearrangements can be used as additional differential diagnostic criteria. Immunohistochemical studies and TCR gamma gene rearrangement analysis using a polymerase chain reaction with primers specific for V gamma 1-8 and V gamma 9 gene segments in combination with denaturing gradient gel electrophoresis (PCR/ DGGE) were performed on frozen material of 11 pseudo-T-cell lymphomas and 17 CTCLs, including 9 cases of mycosis fungoides (MF) and 8 pleomorphic CTCLs. Clonal TCR gamma gene rearrangements were found in 66% of patch/plaque-stage MF and 100% of tumor-stage MF and pleomorphic CTCL, but not in any of 10 pseudo-T-cell lymphomas studied. Aberrant expression of CD2, CD3, and/or CD5 antigens was noted in 3 of 6 (50%) cases of patch/plaque-stage MF, all three cases of tumor-stage MF, and 5 of 8 (62%) pleomorphic CTCLs, but not in any of the 11 pseudo-T-cell lymphomas. Moreover, in pseudo-T-cell lymphomas exhibiting a nodular or diffuse growth pattern, a considerable admixture with reactive CD8+ T cells (15 to 60%), B cells (up to 20%), and macrophages was a characteristic finding. In conclusion, the results of this study suggest that demonstration of clonal TCR gene rearrangements and an aberrant phenotype, as well as demonstration of many admixed CD8+ T cells and B cells can be considered as useful additional criteria in the differentiation between pseudo-T-cell lymphomas and CTCLs.
皮肤假性T细胞淋巴瘤与皮肤T细胞淋巴瘤(CTCL)的鉴别可能极其困难。在本研究中,探讨了异常表型的显示及克隆性T细胞受体γ(TCRγ)基因重排的检测是否可作为额外的鉴别诊断标准。对11例假性T细胞淋巴瘤和17例CTCL(包括9例蕈样肉芽肿(MF)和8例多形性CTCL)的冷冻组织进行了免疫组织化学研究及TCRγ基因重排分析,采用针对Vγ1 - 8和Vγ9基因片段的引物进行聚合酶链反应并结合变性梯度凝胶电泳(PCR / DGGE)。在66%的斑块/斑片期MF、100%的肿瘤期MF和多形性CTCL中发现了克隆性TCRγ基因重排,但在所研究的10例假性T细胞淋巴瘤中均未发现。在6例(50%)斑块/斑片期MF中的3例、所有3例肿瘤期MF以及8例(62%)多形性CTCL中的5例中观察到CD2、CD3和/或CD5抗原的异常表达,但在11例假性T细胞淋巴瘤中均未发现。此外,在呈现结节状或弥漫性生长模式的假性T细胞淋巴瘤中,与反应性CD8 + T细胞(15%至60%)、B细胞(高达20%)和巨噬细胞的大量混合是一个特征性发现。总之,本研究结果表明,克隆性TCR基因重排和异常表型的显示,以及大量混合的CD8 + T细胞和B细胞的显示可被视为假性T细胞淋巴瘤与CTCL鉴别中的有用额外标准。