Kang S K, Chang S E, Choi J H, Sung K J, Moon K C, Koh J K
Department of Dermatology, Asan Medical Center, College of Medicine, University of Ulsan, Seoul, Korea.
Clin Exp Dermatol. 2002 May;27(3):212-5. doi: 10.1046/j.1365-2230.2002.01023.x.
Primary cutaneous T-cell lymphomas, including lymphomatoid papulosis, mycosis fungoides and CD30+ anaplastic large cell lymphoma (ALCL) overlap clinicopathologically and form part of a spectrum of lymphoproliferative disorders. There have been several case reports of these diseases coexisting. We describe a 59-year-old Korean man who presented with a recurrent, solitary CD30+ ALCL of 25 years' duration as well as patch stage mycosis fungoides of 11 years' duration. Such occurrences may represent different clinical manifestations of the same clonal T-cell abnormality, and provide further insight into the pathogenesis of these related disorders.
原发性皮肤T细胞淋巴瘤,包括淋巴瘤样丘疹病、蕈样肉芽肿和CD30+间变性大细胞淋巴瘤(ALCL)在临床病理上相互重叠,是淋巴增殖性疾病谱的一部分。已有数例这些疾病共存的病例报告。我们描述了一名59岁的韩国男性,他患有持续25年的复发性孤立性CD30+ALCL以及持续11年的斑块期蕈样肉芽肿。这种情况可能代表同一克隆性T细胞异常的不同临床表现,并为这些相关疾病的发病机制提供进一步的见解。