Stone G C, Wall B A, Oppliger I R, Wener M H, Jolly S L, Aguirre A, Dwyer R, Simkin P A
University of Washington, Seattle.
Ann Intern Med. 1989 Feb 15;110(4):275-8. doi: 10.7326/0003-4819-110-4-275.
An 82-year-old man and a 34-year-old woman developed subacute, obstructive, fatal vasculopathies characterized by extensive crystalline tissue deposits and monoclonal lambda light chain serum components. Cryocrystalglobulinemia was also present in one patient, and the purified crystals contained only lambda light chain dimers. Although the presentation of these patients resembled that of systemic necrotizing vasculitis, histologic evidence of inflammation was lacking and their subsequent rapid clinical deterioration was not altered by corticosteroid therapy, and in one case cyclophosphamide and plasmapheresis. Both patients died within 3 weeks of presentation.
一名82岁男性和一名34岁女性患上了亚急性、阻塞性、致命性血管病变,其特征为广泛的结晶组织沉积和单克隆λ轻链血清成分。其中一名患者还存在冷球蛋白血症,纯化的晶体仅包含λ轻链二聚体。尽管这些患者的临床表现类似于系统性坏死性血管炎,但缺乏炎症的组织学证据,且皮质类固醇治疗以及一例使用环磷酰胺和血浆置换治疗均未改变他们随后迅速的临床恶化情况。两名患者均在出现症状后的3周内死亡。