Weiss L M, Wood G S, Trela M, Warnke R A, Sklar J
N Engl J Med. 1986 Aug 21;315(8):475-9. doi: 10.1056/NEJM198608213150802.
Lymphomatoid papulosis is a chronic, clinically benign skin disorder that, when examined histologically, is seen to include numerous large, atypical lymphoid cells that display antigenic markers of T lymphocytes. To investigate the disparity between the clinical behavior of this disease and its malignant histologic appearance, we analyzed the DNA from skin lesions of six patients for rearrangements of beta and gamma T-cell receptor genes. Lesions from five of these patients showed between one and three clonal rearrangements for at least one T-cell receptor gene. Three separate biopsy specimens from a single patient showed different patterns of rearrangements for the beta gene in each specimen. Our results indicate that lymphomatoid papulosis is a clonal T-cell lymphoproliferative process that may possibly be multiclonal in origin. We conclude that this disease has both biologic and histologic features consistent with a malignant T-cell neoplasm despite its indolent course.
淋巴瘤样丘疹病是一种慢性、临床良性的皮肤疾病,组织学检查时可见其中包含大量显示T淋巴细胞抗原标志物的大型非典型淋巴细胞。为研究该疾病临床行为与其恶性组织学表现之间的差异,我们分析了6例患者皮肤病变处的DNA,以检测β和γ T细胞受体基因的重排情况。其中5例患者的病变至少有一个T细胞受体基因出现了1至3种克隆性重排。来自一名患者的3份独立活检标本显示,每份标本中β基因的重排模式均不同。我们的结果表明,淋巴瘤样丘疹病是一种克隆性T细胞淋巴增殖性过程,其起源可能为多克隆性。我们得出结论,尽管该病病程进展缓慢,但具有与恶性T细胞肿瘤相符的生物学和组织学特征。