Renal manifestation of tuberous sclerosis complex

被引:45
作者
Bissler, John J. [1 ,2 ]
Kingswood, J. Christopher [3 ]
机构
[1] Univ Tennessee, Dept Pediat, Hlth Sci Ctr, Memphis, TN USA
[2] St Jude Childrens Res Hosp, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] St Georges Univ London, Cardiol Clin Acad Grp, Mol & Clin Sci Res Ctr, London, England
关键词
angiomyolipoma; chronic; kidney disease; renal cystic disease; tuberous sclerosis complex; POLYCYSTIC KIDNEY-DISEASE; PRACTICE RESEARCH DATALINK; CONTIGUOUS GENE SYNDROME; GIANT-CELL ASTROCYTOMA; OF-THE-LITERATURE; PRIMARY CILIA; RETROSPECTIVE COHORT; CONSENSUS CONFERENCE; ECONOMIC BURDEN; STEM-CELLS;
D O I
10.1002/ajmg.c.31654
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tuberous sclerosis complex (TSC) is a tumor predisposition syndrome with significant renal cystic and solid tumor disease. It commonly causes several types of cystic disease and benign tumors (angiomyolipomata) in the kidneys that can both lead to significant premature loss of glomerular filtration rate. The main risks of angiomyolipomata, severe bleeding, loss of renal function, and pulmonary lymphangioleiomyomatosis, can be ameliorated by active surveillance and preemptive therapy with mTOR inhibitors. The cystogenic mechanism may involve primary cilia, but also appears to also involve a majority of normal tubular cells and may be driven by a minority of cells with mutations inactivating both their TSC1 or TSC2 genes. Malignant tumors are rare.
引用
收藏
页码:338 / 347
页数:10
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