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Bilateral cysts in the choroid plexus in a patient with autosomal dominant polycystic kidney disease.

Authors :
Casteleijn NF
Spithoven EM
Rookmaaker MB
Vergouwen MD
Gansevoort RT
Source :
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 2015 May; Vol. 30 (5), pp. 859-60. Date of Electronic Publication: 2014 Aug 07.
Publication Year :
2015

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder, which is associated with cyst formation in several organs, renal function decline and a higher prevalence of intracranial aneurysms. We report a 52-year-old, otherwise healthy, man with ADPKD who had asymptomatic, bilateral, multiple cysts in the choroid plexus, which is an extremely rare abnormality. Recent evidence suggests that the polycystin proteins, which are dysfunctional in ADPKD, are found in ciliated choroid plexus cells that are involved with regulation of cerebrospinal fluid homeostasis. We hypothesize therefore that choroid plexus cysts may be part of the ADPKD phenotype, which has not been described before.<br /> (© The Author 2014. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.)

Details

Language :
English
ISSN :
1460-2385
Volume :
30
Issue :
5
Database :
MEDLINE
Journal :
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Publication Type :
Academic Journal
Accession number :
25104083
Full Text :
https://doi.org/10.1093/ndt/gfu264