Bertoia B, Marin M G, Tinarelli G
Minerva Med. 1985 Jun 30;76(26-27):1289-92.
A case of acquired systemic amyloidosis with monoclonal gammopathy in a woman aged 67 years is reported. Clinical features included macroglossia, restrictive cardiomyopathy, cutaneous purpura and carpal-tunnel syndrome. A short review on amyloidosis appears in the case discussion.
报告了一例67岁女性获得性系统性淀粉样变性伴单克隆丙种球蛋白病。临床特征包括巨舌、限制性心肌病、皮肤紫癜和腕管综合征。病例讨论中对淀粉样变性进行了简要综述。