Rubinstein A, Dauber L G
Oncology. 1983;40(3):195-9. doi: 10.1159/000225724.
A patient with angioimmunoblastic lymphadenopathy was treated with chemotherapy to complete remission for 13 years. A single relapse, self-limited, occurred followed 2 years later by the appearance of a disseminated non-Hodgkin's lymphoma with prominent cutaneous lesions and hypogammaglobulinemia. Cells from the peripheral blood and an affected lymph node were characterized by immunologic studies as deriving from the T8 subset of lymphocytes, suggesting a functional relationship between these suppressor cells and the patient's clinical manifestations.
一名血管免疫母细胞性淋巴结病患者接受化疗后完全缓解达13年。两年后出现一次自限性复发，随后出现伴有明显皮肤损害和低丙种球蛋白血症的播散性非霍奇金淋巴瘤。通过免疫学研究对来自外周血和一个受累淋巴结的细胞进行特征分析，结果表明这些细胞源自淋巴细胞的T8亚群，提示这些抑制性细胞与患者的临床表现之间存在功能关系。
