Isobe T, Matsumoto J, Fujita T, Maeda S, Sugiyama T
Jpn J Med. 1982 Jan;21(1):12-6. doi: 10.2169/internalmedicine1962.21.12.
Six cases of multiple myeloma were studied regarding functions and pathology of the kidney. Glomerular changes were minimal, whereas tubular and interstitial changes were noted in all cases. Tubular cells were degenerative and atrophic in cases excreting more than 3 g BJP daily in the urine. Cases without BJP had only minor changes. The most severe impairment of renal function was found in a patient with Fanconi's syndrome, with hypercalcemia, calcium in the tubules, tubular atrophy and interstitial fibrosis. In attempting to correlate immunoglobulin abnormalities with renal histology, immunoperoxidase staining of immunoglobulin heavy and light chains were done on kidney sections. Glomerular and interstitial tissues gave a definitely negative reaction. In contrast, positive staining of light chain of corresponding type wrs found in the cytoplasma of the tubules and most tubular casts, with different degrees possibly in accord with the amounts of BJP.
对6例多发性骨髓瘤患者的肾脏功能和病理进行了研究。肾小球变化极小,而所有病例均出现肾小管和间质改变。每日尿中排出超过3g本周蛋白(BJP)的病例中,肾小管细胞发生变性和萎缩。无BJP的病例仅有轻微改变。在一名患有范科尼综合征、高钙血症、肾小管内有钙沉积、肾小管萎缩和间质纤维化的患者中发现了最严重的肾功能损害。为了将免疫球蛋白异常与肾脏组织学联系起来,对肾脏切片进行了免疫球蛋白重链和轻链的免疫过氧化物酶染色。肾小球和间质组织呈明确的阴性反应。相比之下,在肾小管细胞质和大多数肾小管管型中发现了相应类型轻链的阳性染色,其程度可能不同,与BJP的量相符。