Robson Alistair
Department of Dermatopathology, St. John's Institute of Dermatology, London, United Kingdom.
Oncology (Williston Park). 2007 Feb;21(2 Suppl 1):9-12.
The diagnosis of cutaneous T-cell lymphoma (CTCL) requires accurate histopathology, including immunocytochemistry, as well as careful clinical appraisal and analysis for T-cell clonality. This paper reviews the key histologic features of mycosis fungoides (MF) and its variants, and of lymphomatoid papulosis (LyP). Mycosis fungoides is an epidermotropic CTCL that evolves through distinct disease stages of patch, plaque, and tumor, often leading to transformation in the final stages. Disease staging is made clinically, and diagnosis may be difficult during the early stages because several common dermatologic conditions share features with MF. Therefore, clinical appraisal plus the presence of characteristic histopathologic features are needed to ensure accurate diagnosis. Clinical information is particularly important in the diagnosis of LyP, as the disease appears malignant histologically, but has a benign clinical course. Several other T-cell lymphomas were defined in a recent classification of these cutaneous lymphomas, and some key features of these disorders are also briefly reviewed.
皮肤T细胞淋巴瘤(CTCL)的诊断需要准确的组织病理学检查,包括免疫细胞化学,以及对T细胞克隆性进行仔细的临床评估和分析。本文综述了蕈样肉芽肿(MF)及其变异型和淋巴瘤样丘疹病(LyP)的关键组织学特征。蕈样肉芽肿是一种亲表皮性CTCL,它通过斑片、斑块和肿瘤等不同疾病阶段演变,常在最后阶段发生转化。疾病分期通过临床进行,早期诊断可能困难,因为几种常见的皮肤病与MF有共同特征。因此,需要临床评估加上特征性组织病理学特征的存在来确保准确诊断。临床信息在LyP的诊断中尤为重要,因为该疾病在组织学上看似恶性,但临床病程良性。在这些皮肤淋巴瘤的近期分类中定义了其他几种T细胞淋巴瘤,本文也简要综述了这些疾病的一些关键特征。