» Articles » PMID: 21152937

Clinical and Molecular Insights into Tuberous Sclerosis Complex Renal Disease

Overview
Journal Pediatr Nephrol
Specialties Nephrology
Pediatrics
Date 2010 Dec 15
PMID 21152937
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Patients with tuberous sclerosis complex are at great risk of developing renal lesions as part of their disease. These lesions include renal cysts and tumors. Significant advances in understanding the cell biology of these renal lesions has already led to clinical trials demonstrating that pharmacological interventions are likely possible. This review focuses on the pathology of these renal lesions, their underlying cell biology, and the possible therapeutic strategies that may prove to significantly improve care for these patients.

Citing Articles

Brachial artery aneurysm and bilateral posterior circulation strokes in a young child with tuberous sclerosis complex.

Meyer J, Graydon A, Muthukumaraswamy C, Jones H BMJ Case Rep. 2023; 16(11).

PMID: 37963668 PMC: 10649671. DOI: 10.1136/bcr-2023-255694.


Arginine depletion attenuates renal cystogenesis in tuberous sclerosis complex model.

Amleh A, Pri Chen H, Watad L, Abramovich I, Agranovich B, Gottlieb E Cell Rep Med. 2023; 4(6):101073.

PMID: 37290438 PMC: 10313931. DOI: 10.1016/j.xcrm.2023.101073.


Single Gene Mutations in or Alter Extracellular Vesicle Production and Trafficking.

Kumar P, Zadjali F, Yao Y, Kottgen M, Hofherr A, Gross K Biology (Basel). 2022; 11(5).

PMID: 35625437 PMC: 9139108. DOI: 10.3390/biology11050709.


Benign Renal Tumors in Pediatric Age Group: Retrospective Analysis.

Menon P, Narasimha Rao K, Nazki S, Behera S, Gupta K, Samujh R J Indian Assoc Pediatr Surg. 2021; 26(6):380-392.

PMID: 34912134 PMC: 8637978. DOI: 10.4103/jiaps.JIAPS_214_20.


Rare variant of genetically confirmed tuberous sclerosis complex presenting with bilateral renal angiomyolipoma in Wünderlich syndrome.

Larrazabal R, Chiu H, Sacdalan D BMJ Case Rep. 2021; 14(8).

PMID: 34344650 PMC: 8336137. DOI: 10.1136/bcr-2021-243380.


References
1.
McCullough D, Scott Jr R, Seybold H . Renal angiomyolipoma (hamartoma): review of the literature and report of 7 cases. J Urol. 1971; 105(1):32-44. DOI: 10.1016/s0022-5347(17)61455-1. View

2.
Pea M, Bonetti F, Martignoni G, Henske E, Manfrin E, Colato C . Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous: the identification of malignant epithelioid angiomyolipoma. Am J Surg Pathol. 1998; 22(2):180-7. DOI: 10.1097/00000478-199802000-00005. View

3.
Shillingford J, Piontek K, Germino G, Weimbs T . Rapamycin ameliorates PKD resulting from conditional inactivation of Pkd1. J Am Soc Nephrol. 2010; 21(3):489-97. PMC: 2831854. DOI: 10.1681/ASN.2009040421. View

4.
Stillwell T, Gomez M, KELALIS P . Renal lesions in tuberous sclerosis. J Urol. 1987; 138(3):477-81. DOI: 10.1016/s0022-5347(17)43234-4. View

5.
TWEEDDALE D, DAWE C, McDonald J, CULP O . Angiolipo-leiomyoma of the kidney; report of a case with observations on histogenesis. Cancer. 1955; 8(4):764-70. DOI: 10.1002/1097-0142(1955)8:4<764::aid-cncr2820080419>3.0.co;2-w. View