Aggressive treatment of severe idiopathic focal segmental glomerulosclerosis

被引:0
作者
Diego H. Aviles
Kimberly C. Irwin
Linda S. Dublin
V. Matti Vehaskari
机构
[1] Department of Pediatrics,
[2] Louisiana State University Medical Center and Children’s Hospital,undefined
[3] New Orleans,undefined
[4] Louisiana,undefined
[5] USA,undefined
[6] Children’s Hospital,undefined
[7] 200 Henry Clay Avenue,undefined
[8] New Orleans,undefined
[9] LA 70118,undefined
[10] USA e-mail: MVehas@mail.peds.lsumc.edu Tel.: +1-504-896-9238,undefined
[11] Fax: +1-504-896-9762,undefined
来源
Pediatric Nephrology | 1999年 / 13卷
关键词
Key words Focal segmental glomerulosclerosis; Chronic renal insufficiency; Proteinuria; Intravenous methylprednisolone; Chlorambucil;
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摘要
 When focal segmental glomerulosclerosis (FSGS) has reached the stage of chronic renal insufficiency, further progression is usually considered inevitable. African-American patients are believed to exhibit a particularly aggressive form of FSGS. We have treated five African-American patients, aged 11–18 years, with FSGS and reduced renal function using intensive intravenous methylprednisolone protocol, combined with chlorambucil in three cases. All patients had a pretreatment creatinine clearance of less than 50 ml/min per 1.73 m2. Three patients responded with normalization of creatinine clearance and serum albumin levels and had no or only minimal proteinuria at latest follow-up. One patient showed no improvement and one patient progressed to end-stage renal disease. These findings indicate, for the first time, that even severe FSGS may respond to aggressive methylprednisolone with or without alkylating agent treatment, and that African-American race does not preclude a favorable response.
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页码:298 / 300
页数:2
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