Miller L D, Brown E C, Arnett F C
J Rheumatol. 1979 Mar-Apr;6(2):225-31.
A patient with a 27-year-history of chronic relapsing Reiter's syndrome who developed secondary amyloidosis is described. While there are only 2 reports of this association in the English literature, additional cases are suggested in the light of our present concepts. The patient represents the only case of clinically apparent secondary amyloidosis among 158 patients with HLA B27 associated arthropathies currently followed at our institution. Our patient's amyloidosis was treated for nearly 1 year with colchicine without response.
本文描述了一名患有慢性复发性赖特综合征27年并继发淀粉样变性的患者。虽然英文文献中仅有2例这种关联的报道,但根据我们目前的认识提示可能还有其他病例。该患者是我们机构目前随访的158例HLA B27相关关节病患者中唯一一例临床明显的继发性淀粉样变性病例。我们的患者接受秋水仙碱治疗淀粉样变性近1年但无反应。