Literature DB >> 12692431

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

Gyun Ho Jeong1, Byoung Seok Park, Taek Kyun Jeong, Seong Kwon Ma, Chung Ho Yeum, Soo Wan Kim, Nam Ho Kim, Ki Chul Choi.   

Abstract

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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Year:  2003        PMID: 12692431      PMCID: PMC3055028          DOI: 10.3346/jkms.2003.18.2.284

Source DB:  PubMed          Journal:  J Korean Med Sci        ISSN: 1011-8934            Impact factor:   2.153


  2 in total

1.  Autosomal dominant polycystic kidney disease with congenital absence of contralateral kidney.

Authors:  A E Sirvent; R Enríquez; F Ardoy; F Amorós; C González; A Reyes
Journal:  Int Urol Nephrol       Date:  2006       Impact factor: 2.370

2.  Case report: Atypical polycystic kidney disease.

Authors:  Christopher Shin; Leonard Berliner
Journal:  Radiol Case Rep       Date:  2021-04-30
  2 in total

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