结节性皮肤狼疮黏蛋白病一例  

Nodular cutaneous lupus mucinosis:a case report

作　　者：于越乾 陈声利 周桂芝[1,2] 刘红 张福仁[1,2] YU Yueqian;CHEN Shengli;ZHOU Guizhi;LIU Hong;ZHANG Furen(Hospital for Skin Diseases,Shandong First Medical University,Jinan 250022,China;Shandong Provincial Institute of Dermatology and Venereology,Shandong Academy of Medical Sciences,Jinan 250022,China)

机构地区：[1]山东第一医科大学附属皮肤病医院,山东济南250022 [2]山东省皮肤病性病防治研究所,山东济南250022

出　　处：《中国麻风皮肤病杂志》2025年第3期207-209,共3页China Journal of Leprosy and Skin Diseases

基　　金：山东省皮肤性病学临床医学研究中心。

摘　　要：结节性皮肤狼疮黏蛋白病(nodular cutaneous lupus mucinosis,NCLM)又名丘疹结节性黏蛋白病,临床表现为红斑狼疮相关的丘疹和结节,组织病理为真皮胶原纤维间黏蛋白弥漫性沉积。该病罕见,于1954年首次被报道,目前中文病例报道共9篇。本文报道1例NCLM青年患者,并回顾国内外报道的NCLM病例特点。Nodular cutaneous lupus mucinosis(NCLM) is also known as papule nodular mucins disease.The clinical manifestations are papules and nodules associated with lupus erythematosus,pathology of dermal collagen fibers mucins diffuse deposits.This rare disease was first reported in 1954,and 9 cases have been reported in China.The complete clinical information,laboratory and histopathological results,diagnosis and treatment plan and prognosis of a young patient with NCLM were reported,and the characteristics of NCLM cases reported at home and abroad were reviewed.

关 键 词：结节性皮肤狼疮黏蛋白病 系统性红斑狼疮 皮肤型红斑狼疮 

分 类 号：R758.62[医药卫生—皮肤病学与性病学]