首页 | 本学科首页   官方微博 | 高级检索  
     


Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work
Authors:Takehiro Takahashi  Yoshihide Asano  Maiko Hirakawa  Kouki Nakamura  Ryosuke Saigusa  Naohiko Aozasa  Hayakazu Sumida  Hideki Fujita  Makoto Sugaya  Aki Ohmori  Jun Shimizu  Shinichi Sato
Affiliation:1. Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan;2. Department of Neurology, University of Tokyo Graduate School of Medicine, Tokyo, Japan
Abstract:Localized scleroderma is an inflammatory disorder affecting the skin and underlying tissues, a certain subset of which develops other autoimmune diseases on the basis of a prominent autoimmune background. We here report a unique case of linear scleroderma presenting with a sclerotic plaque on the left thigh, multiple lymphadenopathy in bilateral inguinal and para‐aortic lymph nodes, and hepatosplenomegaly, who later developed polymyositis. We describe the detailed disease course of our case and discuss the clinical significance of multiple lymphadenopathy in localized scleroderma based on a review of published work.
Keywords:hepatosplenomegaly  immune abnormality  linear scleroderma  lymphadenopathy  polymyositis
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号