Sato K C, Kumakiri M, Koizumi H, Ando M, Ohkawara A, Fujioka Y, Kon T
Department of Dermatology, Hokkaido University School of Medicine, Sapporo, Japan.
Br J Dermatol. 1993 Jun;128(6):686-9. doi: 10.1111/j.1365-2133.1993.tb00266.x.
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.
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。