Nicholson Kimberly M, Patel Keyur P, Duvic Madeleine, Prieto Victor G, Tetzlaff Michael T
Department of Pathology, Division of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
J Cutan Pathol. 2012 Sep;39(9):866-71. doi: 10.1111/j.1600-0560.2012.01954.x. Epub 2012 Jul 19.
Bi-clonality is a rare phenomenon seen in approximately 5% of chronic B-cell lymphoproliferative disorders. Both true bi-clonality and somatic hypermutation resulting in intraclonal evolution have been described. We present the case of a 37-year-old female who developed extranodal marginal zone B-cell lymphoma with immunohistochemical studies showing monotypic immunostaining of plasma cells for immunoglobulin lambda light chain on her right arm in 2008. Three years later, she developed a second focus of extranodal marginal zone B-cell lymphoma on her left arm, but immunohistochemical studies demonstrated monotypic immunostaining of plasma cells for immunoglobulin kappa light chain confirmed after repeat analysis. Evaluation for systemic lymphoma with laboratory and imaging studies was negative. Together, the findings were consistent with bi-clonal, multifocal extranodal primary cutaneous marginal zone B-cell lymphoma. We present this case to highlight a rare phenomenon within primary cutaneous marginal zone lymphomas.
双克隆性是一种罕见现象,约5%的慢性B细胞淋巴增殖性疾病可见此现象。真正的双克隆性以及导致克隆内进化的体细胞超突变均有报道。我们报告一例37岁女性,其于2008年患结外边缘区B细胞淋巴瘤,免疫组化研究显示其右臂浆细胞对免疫球蛋白λ轻链呈单型免疫染色。三年后,她左臂又出现一处结外边缘区B细胞淋巴瘤病灶,但免疫组化研究显示浆细胞对免疫球蛋白κ轻链呈单型免疫染色,重复分析后得以证实。实验室及影像学检查对系统性淋巴瘤的评估为阴性。综合来看,这些发现符合双克隆性、多灶性原发性皮肤边缘区B细胞淋巴瘤。我们呈现此病例以突出原发性皮肤边缘区淋巴瘤内的一种罕见现象。