Lange-Wantzin G, Thomsen K, Hou-Jensen K
Acta Derm Venereol. 1984;64(1):46-51.
A follow-up study has been performed on 16 patients with lymphomatoid papulosis diagnosed at the Finsen Institute during the years 1970-81. In none of the patients did malignant lymphoma develop during the observation period (7 months to 22 years). During this period the nature of the lesions and the tendency to recurrence were unchanged in 11 patients, spontaneous remission took place in 4, and 1 patient went into complete remission after PUVA treatment (8-methoxsalen followed by UVA). The histological material (32 punch biopsies) could be divided into two major groups diagnosed as either typical (16 biopsies) or consistent with lymphomatoid papulosis (16 biopsies). Based on our present knowledge, we suggest the following classification of lymphomatoid papulosis: 1) "classical" lymphomatoid papulosis, 2) lymphomatoid papulosis associated with parapsoriasis en plaque or mycosis fungoides and 3) primary cutaneous T-cell lymphoma.
对1970年至1981年间在芬森研究所确诊的16例淋巴瘤样丘疹病患者进行了一项随访研究。在观察期(7个月至22年)内,没有一例患者发生恶性淋巴瘤。在此期间,11例患者的病变性质和复发倾向未发生变化,4例患者出现自发缓解,1例患者在接受光化学疗法(8-甲氧补骨脂素随后进行紫外线A照射)治疗后完全缓解。组织学材料(32次钻孔活检)可分为两大组,分别诊断为典型(16次活检)或符合淋巴瘤样丘疹病(16次活检)。基于我们目前的认识,我们建议对淋巴瘤样丘疹病进行如下分类:1)“经典”淋巴瘤样丘疹病,2)与斑块状副银屑病或蕈样肉芽肿相关的淋巴瘤样丘疹病,以及3)原发性皮肤T细胞淋巴瘤。