淀粉样变性
医学
关节病
淀粉样蛋白(真菌学)
β-2微球蛋白
发病机制
病理
背景(考古学)
淀粉样疾病
疾病
免疫学
淀粉样纤维
骨关节炎
淀粉样β
生物
古生物学
替代医学
作者
Julio A. Díaz-Pérez,Sheila Conway,Yiqin Zuo,G. Petur Nielsen,Martin K. Selig,Andrew E. Rosenberg
标识
DOI:10.1097/pap.0000000000000317
摘要
Amyloid arthropathy is a joint disease associated with systemic amyloidosis. Herein, we present a model case and review the clinicopathologic features and pathophysiology of this disorder. Amyloid arthropathy results from elevation of serum amyloidogenic proteins and their deposition as aggregates in synovial fluid and articular tissues. The most common proteins are beta-2-microglobulin in the context of long-term hemodialysis therapy and immunoglobulin light chains associated with plasma cell proliferations. We provide a comprehensive update on the pathogenesis, clinical manifestations, and pathologic features of amyloid arthropathy. We provide detailed insights on amyloid protein deposition and aggregation in joints and proper details for diagnosis.
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