Monova D, Belovezhdov N, Minova V, Doĭchinov D
Vutr Boles. 1988;27(6):100-3.
A case is presented of a woman with idiopathic nephrotic syndrome--mesangioproliferative glomerulonephritis who after a 7-year therapeutic remission developed a rapidly progressing (semilunar) glomerulonephritis with a severe nephrotic syndrome, arterial hypertension, anemia, renal failure. The patient was not influenced by the treatment with ordinary doses of glucocorticosteroids and temporarily improved by the combined "pulse" methylprednisolone, immunosuppressive and heparin treatment. The possible pathogenetic mechanisms which may have played a role in the transition of the idiopathic nephrotic syndrome into a rapidly progressing glomerulonephritis are discussed.
本文报告一例患有特发性肾病综合征——系膜增生性肾小球肾炎的女性患者,该患者在经过7年的治疗缓解期后,发展为快速进展性(半月形)肾小球肾炎,并伴有严重肾病综合征、动脉高血压、贫血和肾衰竭。普通剂量糖皮质激素治疗对该患者无效,联合“冲击”甲基强的松龙、免疫抑制和肝素治疗后病情暂时改善。文中讨论了可能在特发性肾病综合征转变为快速进展性肾小球肾炎过程中起作用的发病机制。