Serres J J, Butori P J, Coussement A, Cassuto G P
J Radiol Electrol Med Nucl. 1977 Oct;58(10):641-5.
Angio-immunoblastic lymphadenopathy, which has been recently individualized, is seen clinically as a stade III or IV haematosarcoma. Its etiopathogeny is mysterious and histological diagnosis is often difficult. Lymphography can assist diagnosis for, in an appreciable number of cases, the pictures which appear in association make it possible to distinguish between haematosarcomas occurring in Hodgkin's disease and others.
血管免疫母细胞性淋巴结病，最近已被独立分类，临床上被视为III期或IV期血肉瘤。其病因不明，组织学诊断往往困难。淋巴造影有助于诊断，因为在相当数量的病例中，相关出现的影像能够区分霍奇金病中发生的血肉瘤和其他血肉瘤。
