Luder A S, Cohen S L, Fisher C
Postgrad Med J. 1980 Apr;56(654):282-7. doi: 10.1136/pgmj.56.654.282.
A 35-year-old-man presented with nephrotic syndrome due to mesangiocapillary glomerulonephritis; he later developed a potassium-losing state, generalized amino aciduria and glycosuria. Clinical and biochemical improvement occurred after steroid therapy. The possible pathophysiological mechanisms are discussed.
一名35岁男性因系膜毛细血管性肾小球肾炎出现肾病综合征;他后来发展为失钾状态、全身性氨基酸尿和糖尿。类固醇治疗后临床和生化指标有所改善。文中讨论了可能的病理生理机制。