摘要
患者女,43岁,全身泛发性丘疹、硬化伴瘙痒1年半。皮损组织病理示:真皮内黏蛋白沉积,阿辛兰染色阳性;免疫固定电泳:IgG(+),轻链λ(+);骨髓细胞学检查未见明显异常。诊断:硬化性黏液水肿。
A 43-year-old female presented generalized papules,sclerosis and pruritus for one and a half years.Histopathology examination revealed mucin deposition in the dermis,accompanied by positive alcian blue staining.Immunofixation electrophoresis showed positive of immunoglobulin G and λ light chain.There were no obvious abnormalities in bone marrow cytology examination.Therefore,the patient was diagnosed as scleromyxedema.
作者
张晗
冯永芳
刘雯
黄萌
庹梅
邹亮
陈柳青
ZHANG Han;FENG Yongfang;LIU Wen;HUANG Meng;TUO Mei;ZOU Liang;CHEN Liuqing(Department of Dermatology,Wuhan No.1 Hospital,Wuhan 430022,China)
出处
《中国皮肤性病学杂志》
CAS
CSCD
北大核心
2020年第9期1064-1066,共3页
The Chinese Journal of Dermatovenereology