Mori Akinori, Tamaru Jun-Ichi, Sumi Hajime, Kondo Haruki
Department of Medicine, Shimizu Kohsei Hospital, Shizuoka, Japan.
Eur J Haematol. 2002 Apr;68(4):243-6. doi: 10.1034/j.1600-0609.2002.01667.x.
A case is reported of lymphoplasmacytoid lymphoma (LPL) associated with a monoclonal immunoglobulin (Ig) M and cold agglutinin disease (CAD) that was successfully treated with rituximab. A 52-yr-old male was admitted with a direct antiglobulin test positive haemolytic anaemia and thrombocytopenia associated with monoclonal IgM. Bone marrow examinations disclosed the marked infiltration of medium-sized lymphoma cells with plasmacytoid differentiation that indicated non-Hodgkin's lymphoma of B-cell origin (LPL). Prednisolone and combination chemotherapy were temporarily effective for both anaemia and thrombocytopenia, although these strategies became refractory and bone marrow lymphoplasmacytosis persisted. CAD ameliorated, and the serum level of IgM decreased in association with the disappearance of lymphoma cells and clonal rearrangement of the Ig heavy chains in the bone marrow after treatment with rituximab. Rituximab played a significant role in the treatment of refractory CAD associated with LPL.
报告了1例与单克隆免疫球蛋白(Ig)M和冷凝集素病(CAD)相关的淋巴浆细胞样淋巴瘤(LPL),经利妥昔单抗成功治疗。一名52岁男性因直接抗球蛋白试验阳性的溶血性贫血和与单克隆IgM相关的血小板减少症入院。骨髓检查发现中等大小的淋巴瘤细胞显著浸润,伴有浆细胞样分化,提示B细胞起源的非霍奇金淋巴瘤(LPL)。泼尼松龙和联合化疗对贫血和血小板减少症暂时有效,尽管这些策略变得难治且骨髓淋巴浆细胞增多持续存在。CAD改善,利妥昔单抗治疗后,随着淋巴瘤细胞的消失和骨髓中Ig重链的克隆重排,IgM血清水平下降。利妥昔单抗在治疗与LPL相关的难治性CAD中发挥了重要作用。