Storch H, Püschel W, Raabe F, Schmidt F
Haematologia (Budap). 1986;19(3):219-25.
An extramedullary plasmocytoma in a right inguinal lymph node was observed in a 62-year-old woman. The tumor showed monoclonal proliferation of plasma cells which revealed highly positive stainings of both IgD and lambda light chain using the PAP-technique. Monoclonal IgD-lambda was also secreted in serum and urine. Clinical data, lymphography and bone biopsy showed a tumor spreading in the right inguinal, left iliacal and lumbar regions without systemic involvement of bone. In contrast to extramedullary plasmocytomas of other immunoglobulin classes the disease progressed rapidly and the patient died 8 months after the onset. The present case is the first reported IgD-plasmocytoma in lymph nodes.
一名62岁女性右腹股沟淋巴结出现髓外浆细胞瘤。肿瘤显示浆细胞单克隆增殖,采用PAP技术检测发现其IgD和λ轻链染色均呈强阳性。血清和尿液中也分泌单克隆IgD-λ。临床资料、淋巴造影和骨活检显示肿瘤扩散至右腹股沟、左髂骨和腰部区域,但无骨骼系统受累。与其他免疫球蛋白类别的髓外浆细胞瘤不同,该疾病进展迅速,患者发病8个月后死亡。本病例是首例报道的淋巴结IgD浆细胞瘤。