Mourtzinos Nikki, Puri Puja K, Wang Guanghua, Liu Min-Ling
Department of Pathology, George Washington University Hospital, Washington, DC, USA.
J Cutan Pathol. 2010 Apr;37(4):491-6. doi: 10.1111/j.1600-0560.2009.01323.x. Epub 2009 Jul 10.
Pagetoid reticulosis is an indolent primary cutaneous T-cell lymphoma. It typically presents as a solitary and slowly growing patch or plaque on the extremity, histologically characterized by an acanthotic epidermis infiltrated with atypical lymphocytes. Here, we present histological, immunophenotypical and molecular findings of a 29-year-old Jamaican man with bilateral wrist plaques. Histology showed marked acanthosis, hyperkeratosis and an intraepidermal infiltration consisting of large atypical lymphocytes. Immunohistochemical stains showed CD3 and CD5 positive T cells with significant loss of CD7, double negative CD4 and CD8 and strong positive CD30. Molecular analysis showed a monoclonal T-cell receptor (TCR) gamma gene rearrangement. Review of the literature confirms that the immunophenotype of pagetoid reticulosis is variable with decreasing frequency of CD8+ cytotoxic/suppressor T cell, CD4+ helper T cell and least commonly CD4/CD8 double negative phenotypes. Although CD4/CD8 double negative phenotype appears to be associated with higher proliferation index, it does not appear to confer prognostic significance.
派杰样网状细胞增生症是一种惰性原发性皮肤T细胞淋巴瘤。它通常表现为肢体上的单个且生长缓慢的斑片或斑块,组织学特征为棘层肥厚的表皮中有非典型淋巴细胞浸润。在此,我们展示了一名患有双侧腕部斑块的29岁牙买加男性的组织学、免疫表型和分子学研究结果。组织学显示明显的棘层肥厚、角化过度以及由大量非典型淋巴细胞组成的表皮内浸润。免疫组织化学染色显示CD3和CD5阳性的T细胞,CD7显著缺失,CD4和CD8双阴性,CD30强阳性。分子分析显示单克隆T细胞受体(TCR)γ基因重排。文献回顾证实,派杰样网状细胞增生症的免疫表型是可变的,CD8 + 细胞毒性/抑制性T细胞、CD4 + 辅助性T细胞的频率逐渐降低,最不常见的是CD4/CD8双阴性表型。尽管CD4/CD8双阴性表型似乎与较高的增殖指数相关,但它似乎不具有预后意义。