Tefferi A, Wiltsie J C, Kurtin P J
Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905.
Am J Hematol. 1992 Jul;40(3):232-3. doi: 10.1002/ajh.2830400315.
Lymphocyte predominance Hodgkin's disease (LPHD) can be histologically subdivided into a nodular and diffuse variety. The two subtypes differ in immunophenotypic characteristics but have a similar long-term clinical outcome. Nodular LPHD has immunophenotypic and histological characteristics suggestive of a B-cell derived neoplastic process. Nodular LPHD is associated with an increased risk of secondary large cell lymphoma (LCL). Gene rearrangement studies in some of these cases have revealed a B-cell clonal process, further supporting the association between nodular LPHD and the B-cell system. In addition, it has been suggested that the apparent secondary LCL, at least in some cases, may represent a histologic progression of nodular LPHD. We report a unique case of T-cell lymphoma, confirmed by T-cell receptor gene rearrangement studies, which developed in the setting of nodular LPHD. Our observation demonstrates that the association of nodular LPHD and LCL is complex and that LCL developing in the context of nodular LPHD may be an independent secondary process sometimes involving T-cell lymphomas.
淋巴细胞为主型霍奇金淋巴瘤(LPHD)在组织学上可细分为结节型和弥漫型。这两种亚型在免疫表型特征上有所不同,但长期临床结局相似。结节型LPHD具有提示B细胞来源肿瘤性过程的免疫表型和组织学特征。结节型LPHD与继发大细胞淋巴瘤(LCL)的风险增加有关。对其中一些病例的基因重排研究显示了B细胞克隆过程,进一步支持了结节型LPHD与B细胞系统之间的关联。此外,有人提出,至少在某些情况下,明显的继发LCL可能代表结节型LPHD的组织学进展。我们报告了1例独特的T细胞淋巴瘤病例,经T细胞受体基因重排研究证实,该病例发生于结节型LPHD背景下。我们的观察表明,结节型LPHD与LCL的关联很复杂,在结节型LPHD背景下发生的LCL可能是一个独立的继发过程,有时涉及T细胞淋巴瘤。