Improvement in Renal Cystic Disease of Tuberous Sclerosis Complex After Treatment with Mammalian Target of Rapamycin Inhibitor

被引:23
|
作者
Siroky, Brian J. [1 ,2 ]
Towbin, Alexander J. [3 ]
Trout, Andrew T. [3 ]
Schaefer, Hannah [4 ]
Thamann, Anna R. [1 ]
Agricola, Karen D. [2 ]
Tudor, Cynthia [2 ]
Capal, Jamie [2 ]
Dixon, Bradley P. [1 ]
Krueger, Darcy A. [2 ]
Franz, David N. [2 ]
机构
[1] Cincinnati Childrens Hosp, Med Ctr, Div Nephrol & Hypertens, Cincinnati, OH USA
[2] Cincinnati Childrens Hosp, Med Ctr, Div Neurol, Cincinnati, OH USA
[3] Cincinnati Childrens Hosp, Med Ctr, Dept Radiol, Cincinnati, OH USA
[4] Ludwig Maximilians Univ Munchen, Div Nephrol, Munich, Germany
来源
JOURNAL OF PEDIATRICS | 2017年 / 187卷
关键词
POLYCYSTIC KIDNEY-DISEASE; GIANT-CELL ASTROCYTOMAS; DOUBLE-BLIND; EVEROLIMUS; ANGIOMYOLIPOMA; MULTICENTER; SIROLIMUS; FAILURE; PHASE-3; TSC2;
D O I
10.1016/j.jpeds.2017.05.015
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Renal cysts occur in approximately 50% of patients with tuberous sclerosis complex, but their clinical significance and response to treatment are unknown. Abdominal imaging of 15 patients with tuberous sclerosis complex-associated renal cystic disease who had received mammalian target of rapamycin inhibitor therapy for other tuberous sclerosis complex-related indications was evaluated. Reductions in cyst number, sum diameter, and volume were observed.
引用
收藏
页码:318 / +
页数:7
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