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

نویسندگان

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

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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عنوان ژورنال:
  • Journal of Korean Medical Science

دوره 18  شماره 

صفحات  -

تاریخ انتشار 2003