Suppr超能文献

苔藓样皮肤病变作为长期血液透析患者β2-微球蛋白诱导的淀粉样变性的一个体征。

Lichenoid skin lesions as a sign of beta 2-microglobulin-induced amyloidosis in a long-term haemodialysis patient.

作者信息

Sato K C, Kumakiri M, Koizumi H, Ando M, Ohkawara A, Fujioka Y, Kon T

机构信息

Department of Dermatology, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Br J Dermatol. 1993 Jun;128(6):686-9. doi: 10.1111/j.1365-2133.1993.tb00266.x.

Abstract

We report a case of beta 2-microglobulin-induced amyloidosis. The patient was a 40-year-old man suffering from non-amyloid nephropathy, who had been treated by haemodialysis for 20 years. Lichenoid skin lesions, consisting of groups of pin-head-sized shiny papules, were present on the arms and trunk. On histological examination, amyloid deposits were present, principally in the dermal papillae, but also around the sweat ducts and hair follicles. The amyloid displayed potassium-permanganate-resistant Congo red affinity, and green birefringence under polarized light. Immunohistochemically, beta 2-microglobulin was demonstrated in the lesions, confirming that they were a manifestation of beta 2-microglobulin-associated amyloidosis. Skin lesions of this type have not been reported previously in beta 2-microglobulin-associated amyloidosis.

摘要

我们报告一例β2-微球蛋白诱导的淀粉样变性病。患者为一名40岁男性,患有非淀粉样肾病,已接受血液透析治疗20年。手臂和躯干出现苔藓样皮肤损害,由针头大小的发亮丘疹群组成。组织学检查显示存在淀粉样沉积物,主要位于真皮乳头,但也见于汗腺导管和毛囊周围。淀粉样物质对高锰酸钾具有抗性刚果红亲和力,在偏振光下呈绿色双折射。免疫组织化学显示病变中有β2-微球蛋白,证实它们是β2-微球蛋白相关淀粉样变性病的一种表现。此前尚未有β2-微球蛋白相关淀粉样变性病出现这种类型皮肤损害的报道。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验