伴多发性骨髓瘤的原发性系统性淀粉样变一例  

Primary systemic amyloidosis with multiple myeloma: a case report

作　　者：成春梅 徐静 马琼 倪昌雯 CHENG Chunmei;XU Jing;MA Qiong;NI Changwen(Clinical Medical College,Dali University,Dali 671000,China;Department of Pathology,First Affiliated Hospital of Dali University,Dali 671000,China)

机构地区：[1]大理大学临床医学院,云南大理671000 [2]大理大学第一附属医院皮肤科,云南大理671000

出　　处：《中国麻风皮肤病杂志》2023年第10期737-740,共4页China Journal of Leprosy and Skin Diseases

基　　金：云南省教育厅科学研究基金项目(编号:2022J0701)。

摘　　要：原发性系统性淀粉样变是一种罕见的单克隆浆细胞病,早期症状缺乏特异性,临床容易误诊。本文报道一例以皮肤紫癜、甲受损、充血性心力衰竭为主要特征的伴多发性骨髓瘤的原发性系统性淀粉样变的临床病例。Primary systemic amyloidosis is a disease of rare monoclonal plasma cell,the early symptoms lack specificity and clinically easily misdiagnosed.We report a clinical case of primary systemic amyloidosis with multiple myeloma characterized by purpura,nail damage,and congestive heart failure.

关 键 词：免疫球蛋白轻链型淀粉样变 系统性淀粉样变 多发性骨髓瘤 紫癜 

分 类 号：R733.3[医药卫生—肿瘤] R597.2[医药卫生—临床医学]