Sterry W, Siebel A, Mielke V
Department of Dermatology, University of Kiel, Germany.
Br J Dermatol. 1992 May;126(5):456-62. doi: 10.1111/j.1365-2133.1992.tb15116.x.
The peripheral T-cell lymphomas represent a heterogeneous group and include, besides mycosis fungoides and Sézary syndrome, large-cell anaplastic lymphoma. We report 15 cases from our files that fulfil the histological criteria of pleomorphic T-cell lymphoma with primary skin involvement. Most of the cases were elderly with a male-to-female ratio of 1.5:1. The HTLV-1 serology was negative. The clinical features of these patients differed from those with mycosis fungoides and Sézary syndrome, in that eczematous and precursor lesions such as parapsoriasis en plaque were lacking apart from one exception. All the patients with small-cell pleomorphic T-cell lymphomas were alive, although three of the nine patients with medium-to-large tumour cells have died. Pleomorphic T-cell lymphoma should be regarded as a distinct entity among the lymphoproliferative disorders of the skin.
外周T细胞淋巴瘤是一组异质性疾病,除蕈样肉芽肿和 Sézary 综合征外,还包括大细胞间变性淋巴瘤。我们报告了15例符合原发性皮肤受累的多形性T细胞淋巴瘤组织学标准的病例,这些病例来自我们的病例档案。大多数病例为老年人,男女比例为1.5:1。HTLV-1血清学检测为阴性。这些患者的临床特征与蕈样肉芽肿和 Sézary 综合征患者不同,除1例例外,均无湿疹样病变和前期病变,如斑块状副银屑病。所有小细胞多形性T细胞淋巴瘤患者均存活,尽管9例有中至大肿瘤细胞的患者中有3例死亡。多形性T细胞淋巴瘤应被视为皮肤淋巴增殖性疾病中的一种独特实体。