Banik S, Ward R L, Hasleton P S
J Clin Pathol. 1979 Nov;32(11):1110-20. doi: 10.1136/jcp.32.11.1110.
A case of immunoblastic lymphadenopathy which underwent transformation into immunoblastic sarcoma is reported. A 64-year-old man presented with a rash, generalised lymphadenopathy, and hepatosplenomegaly. A cervical lymph node removed at biopsy showed the features of immunoblastic lymphadenopathy with the presence of heavy chain classes IgG, IgM, and IgA and both kappa and lambda light chain types in the cytoplasm of the immunoblasts. No such immunoglobulins could be demonstrated in the lymph nodes obtained at necropsy when the patient died of widespread immunoblastic sarcoma. The biological evolution and histogenesis of the disease are discussed and the current literature is reviewed.
报告了一例免疫母细胞性淋巴结病转化为免疫母细胞肉瘤的病例。一名64岁男性出现皮疹、全身淋巴结肿大和肝脾肿大。活检切除的颈部淋巴结显示出免疫母细胞性淋巴结病的特征,免疫母细胞胞质内存在IgG、IgM和IgA重链类别以及kappa和lambda轻链类型。当患者死于广泛播散的免疫母细胞肉瘤时,尸检获得的淋巴结中未发现此类免疫球蛋白。讨论了该疾病的生物学演变和组织发生,并回顾了当前的文献。