论文部分内容阅读
本文报道3例儿童血管免疫母细胞淋巴结病。该病特征是发热、皮疹、肝脾肿大、全身性淋巴结肿大。免疫学检查显示血清γ球蛋白和免疫球蛋白升高。淋巴结病理改变是特异性的。确诊须靠淋巴结活体组织检查。本病目前无特效治疗。3例患儿于住院期间给予“CVP”(cytoxan,vincristinum,prednisonum)联合化疗,近期疗效尚好。本病预后不良。
This article reports three cases of children with immunoblastic lymphocytic disease. The disease is characterized by fever, rash, hepatosplenomegaly, systemic lymphadenopathy. Immunological tests showed elevated serum gamma globulin and immunoglobulin. Pathological changes in lymph nodes are specific. Diagnosis must rely on lymph node biopsy. The disease is currently no effective treatment. Three patients were given “CVP” (cytoxan, vincristinum, prednisonum) in combination with chemotherapy during their hospital stay, and the immediate effect was good. Poor prognosis of the disease.