Roggero E, Zucca E, Mainetti C, Bertoni F, Valsangiacomo C, Pedrinis E, Borisch B, Piffaretti J C, Cavalli F, Isaacson P G
Istituto Oncologico Svizzera Italiana, Department of Medical Oncology, Ospedale San Giovanni, Bellinzona, Switzerland.
Hum Pathol. 2000 Feb;31(2):263-8. doi: 10.1016/s0046-8177(00)80233-6.
Primary cutaneous B-cell lymphomas have been associated with Borrelia burgdorferi, the spirochete responsible for Lyme disease. Recently, cutaneous marginal zone B-cell lymphoma has been proposed as a distinct clinical-pathological entity. We report a case of primary cutaneous marginal zone lymphoma, associated with B burgdorferi infection. Polymerase chain reaction (PCR) amplification of the third complementarity determining region (CDR3) of the immunoglobulin heavy chain gene showed the presence of a monoclonal lymphoproliferation, therefore strengthening the histological diagnosis of a malignant process. B burgdorfer-specific hbb gene sequences were detected by PCR in the lymphoma tissue at diagnosis but not after antibiotic treatment. A nearly complete clinical and histological regression was observed after B burgdorferi eradication, with immunohistochemistry studies showing disappearance of plasma cell differentiation and a marked decline in the number of CD3+ T cells and Ki-67+ cells. Our case confirms the link between B burgdorferi and some cutaneous lymphomas. The disappearance of the microorganism accompanied by the unequivocal decrease of most indicators of active T- and B-cell immune response strongly supported a pathogenetic role for B burgdorferi in sustaining an antigen-driven development and growth of this cutaneous marginal zone lymphoma. Antibiotic therapy (analogous to Helicobacter pylori infection in gastric MALT lymphoma) might be helpful with the aim of averting or at least deferring the indication for more aggressive treatment.
原发性皮肤B细胞淋巴瘤与莱姆病的病原体伯氏疏螺旋体有关。最近,皮肤边缘区B细胞淋巴瘤被认为是一种独特的临床病理实体。我们报告一例与伯氏疏螺旋体感染相关的原发性皮肤边缘区淋巴瘤病例。免疫球蛋白重链基因第三互补决定区(CDR3)的聚合酶链反应(PCR)扩增显示存在单克隆淋巴细胞增殖,从而强化了恶性病变的组织学诊断。诊断时在淋巴瘤组织中通过PCR检测到伯氏疏螺旋体特异性hbb基因序列,但抗生素治疗后未检测到。根除伯氏疏螺旋体后观察到近乎完全的临床和组织学缓解,免疫组化研究显示浆细胞分化消失,CD3+T细胞和Ki-67+细胞数量显著下降。我们的病例证实了伯氏疏螺旋体与某些皮肤淋巴瘤之间的联系。微生物的消失伴随着活跃的T细胞和B细胞免疫反应的大多数指标明确下降,有力地支持了伯氏疏螺旋体在维持这种皮肤边缘区淋巴瘤的抗原驱动发展和生长中起致病作用。抗生素治疗(类似于胃黏膜相关淋巴组织淋巴瘤中的幽门螺杆菌感染)可能有助于避免或至少推迟更积极治疗的指征。