Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequently occurring hereditary kidney disease, and axial spondyloarthritis (SpA) is one of the most frequently occurring rheumatic diseases. Treatment-related decisions for axial SpA may pose a challenge in case of renal involvement....

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Autores principales: Yurdakul, Ozan Volkan, Tamer, Abdulkerim Furkan, Küçükakkaş, Okan, Rezvani, Aylin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857328/
https://www.ncbi.nlm.nih.gov/pubmed/29686921
http://dx.doi.org/10.1155/2018/6150875
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author Yurdakul, Ozan Volkan
Tamer, Abdulkerim Furkan
Küçükakkaş, Okan
Rezvani, Aylin
author_facet Yurdakul, Ozan Volkan
Tamer, Abdulkerim Furkan
Küçükakkaş, Okan
Rezvani, Aylin
author_sort Yurdakul, Ozan Volkan
collection PubMed
description Autosomal dominant polycystic kidney disease (ADPKD) is the most frequently occurring hereditary kidney disease, and axial spondyloarthritis (SpA) is one of the most frequently occurring rheumatic diseases. Treatment-related decisions for axial SpA may pose a challenge in case of renal involvement. The authors describe two siblings with cooccurrence of these two diseases. The association of these two diseases is not well known. Practitioners should monitor renal function in SpA patients and take treatment-related decisions regarding renal involvement. Antitumor necrosis factor-alpha (anti-TNF-α) agents may be used in case nonsteroidal anti-inflammatory drugs (NSAIDs) cannot be utilized.
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spelling pubmed-58573282018-04-23 Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence Yurdakul, Ozan Volkan Tamer, Abdulkerim Furkan Küçükakkaş, Okan Rezvani, Aylin Case Rep Rheumatol Case Report Autosomal dominant polycystic kidney disease (ADPKD) is the most frequently occurring hereditary kidney disease, and axial spondyloarthritis (SpA) is one of the most frequently occurring rheumatic diseases. Treatment-related decisions for axial SpA may pose a challenge in case of renal involvement. The authors describe two siblings with cooccurrence of these two diseases. The association of these two diseases is not well known. Practitioners should monitor renal function in SpA patients and take treatment-related decisions regarding renal involvement. Antitumor necrosis factor-alpha (anti-TNF-α) agents may be used in case nonsteroidal anti-inflammatory drugs (NSAIDs) cannot be utilized. Hindawi 2018-03-04 /pmc/articles/PMC5857328/ /pubmed/29686921 http://dx.doi.org/10.1155/2018/6150875 Text en Copyright © 2018 Ozan Volkan Yurdakul et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yurdakul, Ozan Volkan
Tamer, Abdulkerim Furkan
Küçükakkaş, Okan
Rezvani, Aylin
Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence
title Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence
title_full Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence
title_fullStr Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence
title_full_unstemmed Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence
title_short Axial Spondyloarthritis and Autosomal Dominant Polycystic Kidney Disease in Two Siblings: A Rare Cooccurrence
title_sort axial spondyloarthritis and autosomal dominant polycystic kidney disease in two siblings: a rare cooccurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857328/
https://www.ncbi.nlm.nih.gov/pubmed/29686921
http://dx.doi.org/10.1155/2018/6150875
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