Murakami M, Sugiura K
Rinsho Ketsueki. 1989 Jan;30(1):116-21.
A case of immunoblastic lymphadenopathy like T cell lymphoma (IBL like T cell lymphoma) associated with biclonal gammopathy is reported. The patient is a 79 year-old male who was admitted to our hospital for generalized lymphadenopathy in January 1987. The lymph node biopsy revealed complete architectural effacement with replacement by a diffuse cellular infiltrate of immunoblasts and pale cells which have a T cell phenotype. A diagnosis of IBL like T cell lymphoma was made. Of interest, high serum level of IgG (6,630 mg/dl) was noted, and immunoelectrophoresis revealed biclonal gammopathy (IgG kappa, IgG lambda), but no remarkable abnormalities were found in the bone marrow aspiration and bone survey. We treated the patient with two courses of CHOP therapy, which resulted in marked improvement of generalized lymphadenopathy and disappearance of biclonal gammopathy. However, relapse was noted a month later without reappearance of biclonal gammopathy. The rebiopsy of lymph node revealed a new appearance of Lennert's lesions and decrease of immunoblasts in number. The patient received two courses of M-BACOD therapy, which achieved complete remission, and the patient remained in remission for more than 17 months.
报告了一例与双克隆丙种球蛋白病相关的免疫母细胞性淋巴结病样T细胞淋巴瘤(IBL样T细胞淋巴瘤)。患者为79岁男性,1987年1月因全身淋巴结肿大入院。淋巴结活检显示结构完全消失,被免疫母细胞和具有T细胞表型的淡染细胞的弥漫性细胞浸润所取代。诊断为IBL样T细胞淋巴瘤。有趣的是,发现血清IgG水平较高(6630mg/dl),免疫电泳显示双克隆丙种球蛋白病(IgG κ,IgG λ),但骨髓穿刺和骨扫描未发现明显异常。我们用两疗程的CHOP方案治疗该患者,全身淋巴结肿大明显改善,双克隆丙种球蛋白病消失。然而,一个月后复发,双克隆丙种球蛋白病未再次出现。淋巴结再次活检显示出现新的Lennert病变,免疫母细胞数量减少。患者接受了两疗程的M-BACOD方案治疗,达到完全缓解,患者缓解超过17个月。