Petrella Tony, Maubec Eve, Cornillet-Lefebvre Pascale, Willemze Rein, Pluot Michel, Durlach Anne, Marinho Eduardo, Benhamou Jean-Luc, Jansen Patty, Robson Alistair, Grange Florent
Department of Pathology of Dijon's University Hospital and the Centre de Pathologie of Dijon, 2100-DIJON, France.
Am J Surg Pathol. 2007 Dec;31(12):1887-92. doi: 10.1097/PAS.0b013e318068b527.
The authors report 4 cases of cutaneous lymphoproliferation unusual by their histology and their clinical presentation. Each presented with a history of a slow growing nodule on the ear. Despite the indolent clinical evolution, the histology suggested a high-grade lymphoma. All lesions consisted of a dense, diffuse proliferation of monomorphous medium-sized T cells throughout the dermis and subcutis. There was no epidermotropism and a grenz zone was clearly present in each case. The tumor cells displayed irregular blastlike nuclei, with small nucleoli and clear chromatin and had a CD3+, CD8+, CD4+, TIA1+, granzyme B(-)immunophenotype with a loss of other T-cell antigens. The 3 cases with available material for polymerase chain reaction studies displayed a monoclonal T-cell rearrangement of the T-cell receptor-gamma chain. These cases do not correspond to a recognized cutaneous T-cell lymphoma as described in the recent WHO/EORTC classification. The apparent striking propensity for the ear suggests that they might represent a specific entity. Further cases are needed to confirm this hypothesis. It is important for such indolent lesions to be known to avoid over treatment.
作者报告了4例皮肤淋巴细胞增生性疾病,其组织学和临床表现均不寻常。每例均有耳部缓慢生长结节的病史。尽管临床进展缓慢,但组织学提示为高级别淋巴瘤。所有病变均由整个真皮和皮下组织中密集、弥漫性增生的单形性中等大小T细胞组成。无亲表皮现象,每例均可见无细胞带。肿瘤细胞显示核呈不规则母细胞样,核仁小,染色质清晰,免疫表型为CD3 +、CD8 +、CD4 +、TIA1 +、颗粒酶B(-),其他T细胞抗原缺失。3例有材料可用于聚合酶链反应研究的病例显示T细胞受体γ链的单克隆T细胞重排。这些病例与最近世界卫生组织/欧洲癌症研究与治疗组织分类中描述的公认皮肤T细胞淋巴瘤不符。耳部明显的显著倾向表明它们可能代表一种特殊的实体。需要更多病例来证实这一假设。了解此类惰性病变很重要,以避免过度治疗。