Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases of unilateral ADPKD with agenesis of contralateral kidney have been reported. We present a case...

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Detalles Bibliográficos
Autores principales: Jeong, Gyun Ho, Park, Byoung Seok, Jeong, Taek Kyun, Ma, Seong Kwon, Yeum, Chung Ho, Kim, Soo Wan, Kim, Nam Ho, Choi, Ki Chul
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2003
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055028/
https://www.ncbi.nlm.nih.gov/pubmed/12692431
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author Jeong, Gyun Ho
Park, Byoung Seok
Jeong, Taek Kyun
Ma, Seong Kwon
Yeum, Chung Ho
Kim, Soo Wan
Kim, Nam Ho
Choi, Ki Chul
author_facet Jeong, Gyun Ho
Park, Byoung Seok
Jeong, Taek Kyun
Ma, Seong Kwon
Yeum, Chung Ho
Kim, Soo Wan
Kim, Nam Ho
Choi, Ki Chul
author_sort Jeong, Gyun Ho
collection PubMed
description Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases of unilateral ADPKD with agenesis of contralateral kidney have been reported. We present a case of unilateral ADPKD with agenesis of contralateral kidney in a 66-yr-old man. Radiographic images showed the enlarged right kidney with multiple variable-sized cysts and the absence of the left kidney. The diagnosis of ADPKD was confirmed by the family screening. The patient received maintenance hemodialysis for endstage renal disease. We report a case of unilateral ADPKD associated with contralateral renal agenesis in a 66-yr-old male patient with a literature review.
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spelling pubmed-30550282011-03-15 Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report. Jeong, Gyun Ho Park, Byoung Seok Jeong, Taek Kyun Ma, Seong Kwon Yeum, Chung Ho Kim, Soo Wan Kim, Nam Ho Choi, Ki Chul J Korean Med Sci Research Article Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases of unilateral ADPKD with agenesis of contralateral kidney have been reported. We present a case of unilateral ADPKD with agenesis of contralateral kidney in a 66-yr-old man. Radiographic images showed the enlarged right kidney with multiple variable-sized cysts and the absence of the left kidney. The diagnosis of ADPKD was confirmed by the family screening. The patient received maintenance hemodialysis for endstage renal disease. We report a case of unilateral ADPKD associated with contralateral renal agenesis in a 66-yr-old male patient with a literature review. Korean Academy of Medical Sciences 2003-04 /pmc/articles/PMC3055028/ /pubmed/12692431 Text en
spellingShingle Research Article
Jeong, Gyun Ho
Park, Byoung Seok
Jeong, Taek Kyun
Ma, Seong Kwon
Yeum, Chung Ho
Kim, Soo Wan
Kim, Nam Ho
Choi, Ki Chul
Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
title Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
title_full Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
title_fullStr Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
title_full_unstemmed Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
title_short Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
title_sort unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: a case report.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3055028/
https://www.ncbi.nlm.nih.gov/pubmed/12692431
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