Hofmann-Guilaine C, Nochy D, Jacquot C, Tricottet V, Bariety J, Camilleri J P
Pathol Res Pract. 1985 Aug;180(2):214-9. doi: 10.1016/S0344-0338(85)80177-1.
Up to now, light chain deposition disease (L.C.D.D.) and amyloidosis have been shown to occur in different individuals. A case of association is described in a 76 year old man with terminal renal failure and normal size kidneys. Percutaneous renal biopsy showed glomerular and peritubular fixation of labeled antikappa light chain serum. Stains for amyloidosis were positive in small vessels. Kappa free chains were found in both serum and urine and the bone marrow showed predominantly kappa-containing plasma cells. By electron microscopy both electron-dense granular deposits and amyloid like fibrils were found in the wall of arterioles and small arteries.
到目前为止,轻链沉积病(LCDD)和淀粉样变性已被证明发生在不同个体中。本文描述了一例76岁终末期肾衰竭且肾脏大小正常男性患者出现两者关联的病例。经皮肾活检显示标记的抗κ轻链血清在肾小球和肾小管周围固定。淀粉样变性染色在小血管中呈阳性。血清和尿液中均发现κ游离链,骨髓中主要为含κ的浆细胞。通过电子显微镜检查,在小动脉和小动脉壁中发现了电子致密颗粒沉积物和淀粉样纤维。