Ghiringhelli P, Margaroli P, Crivelli F, Zampatti C
Ospedale Provinciale, Gallarate.
Minerva Med. 1989 Sep;80(9):1035-43.
Of the two cases of angioimmunoblastic lymphadenopathy described, one had arisen after infection by a non-A non-B hepatitis virus and HIV. The possible cause of the immunological changes that triggered the disease are discussed as are its clinical picture, course and treatment. In the first case a 6 month remission period was obtained after a short cycle of cortisone treatment, a second remission followed treatment with CVP. Unfortunately the bronchial pneumonia that followed the second cycle proved fatal. The second case featured recurring infections of the middle ear and respiratory tract causing the patient's death about a year after the onset of the disease.
在所描述的两例血管免疫母细胞性淋巴结病中,一例在感染非甲非乙型肝炎病毒和人类免疫缺陷病毒后发病。文中讨论了引发该疾病的免疫变化的可能原因以及其临床表现、病程和治疗方法。第一例患者在短期使用可的松治疗后获得了6个月的缓解期,第二次缓解是在接受CVP治疗后出现的。不幸的是,第二个疗程后发生的支气管肺炎导致了患者死亡。第二例患者的中耳和呼吸道反复感染,在疾病发作约一年后导致患者死亡。