血管免疫母细胞性淋巴结病：一例长达17年随访的病例
Angio-immunoblastic lymphadenopathy: a case with a 17-year follow-up.
作者信息
Ochshorn M, Michalevicz R, Tchetchik M, Behar A, Seligsohn U
出版信息
Postgrad Med J. 1982 Jun;58(680):367-70. doi: 10.1136/pgmj.58.680.367.
Abstract
A case of angioimmunoblastic lymphadenopathy with a 17-year follow-up is reported. The patient, who first presented with benign hypergammaglobulinaemic purpura of Waldenstrom and autoimmune haemolytic anaemia appears to be the longest survivor with this condition reported so far. The marked variations in the clinical course of patients with angio-immunoblastic lymphadenopathy in conjunction with immunological characteristics are discussed.
摘要
报告了1例血管免疫母细胞性淋巴结病患者，随访长达17年。该患者最初表现为瓦尔登斯特伦良性高球蛋白血症性紫癜和自身免疫性溶血性贫血，似乎是目前报道的患有此病的最长存活者。本文讨论了血管免疫母细胞性淋巴结病患者临床病程的显著差异及其免疫学特征。
Zotero 插件