MacDonald D M, Black M M, Ramnarain N
Br J Dermatol. 1977 Jun;96(6):635-41. doi: 10.1111/j.1365-2133.1977.tb05208.x.
Immunofluorescence studies were carried out on 47 patients with primary localized cutaneous amyloidosis. The majority had the macular, maculopapular or papular forms of lichen amyloidosus, although 3 patients had the nodular type. All biopsies fluoresced positively for immunoglobulins or complement, particularly IgM and C3. Staining for kappa and lambda light chains was positive. The consistent immunofluorescent patterns observed were similar in some respects to lichen planus, suggesting that colloid bodies and amyloid may share similar properties in acting as a filamentous sponge on to which immunoglobulins and complement are absorbed. The pathogenesis of lichen amyloidosus is compared with that of lichen planus.
对47例原发性局限性皮肤淀粉样变患者进行了免疫荧光研究。大多数患者患有苔藓样淀粉样变的斑疹、斑丘疹或丘疹型,不过有3例患者为结节型。所有活检标本的免疫球蛋白或补体呈阳性荧光,尤其是IgM和C3。κ和λ轻链染色呈阳性。观察到的一致免疫荧光模式在某些方面与扁平苔藓相似,这表明胶样小体和淀粉样物质在作为吸收免疫球蛋白和补体的丝状海绵方面可能具有相似的特性。将苔藓样淀粉样变的发病机制与扁平苔藓的发病机制进行了比较。