Tuberous sclerosis complex-associated kidney disease in children

被引:0
|
作者
Marlais, Matko [1 ,2 ]
Mekahli, Djalila [3 ,4 ]
机构
[1] Great Ormond St Hosp Children NHS Fdn Trust, Dept Paediat Nephrol, Great Ormond St, London WC1N 3JH, England
[2] UCL, UCL Great Ormond St Inst Child Hlth, London, England
[3] Katholieke Univ Leuven, Lab Ion Channel Res, Dept Cellular & Mol Med, PKD Res Grp, Louvain, Belgium
[4] Univ Hosp Leuven, Dept Paediat Nephrol, Louvain, Belgium
关键词
Tuberous sclerosis; Imaging; Kidney; Child; Genetics; RENAL CYSTIC-DISEASE; DIAGNOSTIC-CRITERIA; BLOOD-PRESSURE; MANAGEMENT; ANGIOMYOLIPOMA; RECOMMENDATIONS; SURVEILLANCE; EVEROLIMUS; GROWTH;
D O I
10.1007/s00467-024-06642-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder which can have manifestations in the kidneys, along with other organ systems. Children with TSC may develop kidney lesions at any point during childhood, and typically these are angiomyolipomata (AML) and/or kidney cysts. Children may also have hypertension associated with TSC-associated kidney disease, and rarely reduced kidney function. New guidelines for the management of TSC-associated kidney disease in children and adults were published in 2024. This educational review summarises the relevant clinical aspects of these guidelines for paediatric nephrologists through a series of four clinical cases. These cases cover management of hypertension, frequency of follow-up and frequency of kidney imaging. Difficult clinical scenarios are reviewed, such as the management of TSC2-PKD1 contiguous gene syndrome and the management of large AMLs in children with TSC.Graphical abstractA higher resolution version of the Graphical abstract is available as Supplementary information
引用
收藏
页码:1871 / 1877
页数:7
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