Diebold J, Tulliez M, Audouin J, Tricot G, Monsus M, Vilde F, Dubrisay J, Patri B, Arkwright S
Bull Cancer. 1980;67(2):131-8.
A case clinically and morphologically typical angio-immunoblastic lymphadenopathy in a 64-year old man is reported. A sicca syndrome was discovered with histological localization in the labial accessory salivary glands. Death occurred after a course of a few months. The autopsy showed an association of angio-immunoblastic lymphadenopathy lesions of the bone marrow and the lymph node and of typical multivisceral localizations of Kaposi's sarcoma (lymph node, liver, thyroïdd gland) without skin involvement. This association of two diseases characterized by severe dysimmunity with B lymphocytes hyperplasia is discussed, and compared to the others diseases which could be associated with Kaposi's sarcoma.
报告了一例64岁男性临床上和形态学上典型的血管免疫母细胞性淋巴结病病例。发现伴有唇腺组织学定位的干燥综合征。病程数月后死亡。尸检显示骨髓和淋巴结的血管免疫母细胞性淋巴结病病变与卡波西肉瘤的典型多脏器定位(淋巴结、肝脏、甲状腺)相关,无皮肤受累。讨论了这两种以严重免疫失调伴B淋巴细胞增生为特征的疾病的关联,并与其他可能与卡波西肉瘤相关的疾病进行了比较。