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Unilateral renal cystic disease in adults
Author(s) -
Dae Yeon Hwang,
Curie Ahn,
Jung Geon Lee,
Seung Hyup Kim,
Ha Young Oh,
Y. Kim,
E. S. Lee,
Jin Suk Han,
Suhnggwon Kim,
Jung Sang Lee
Publication year - 1999
Publication title -
nephrology dialysis transplantation
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/14.8.1999
Subject(s) - medicine , autosomal dominant polycystic kidney disease , differential diagnosis , renal function , disease , polycystic kidney disease , abdominal ultrasonography , ultrasonography , kidney , family history , cystic kidney disease , pathology , radiology
Unilateral renal cystic disease (URCD) is morphologically indistinguishable from autosomal dominant polycystic kidney disease (ADPKD) except for its unilaterality. Unlike ADPKD, URCD patients show neither a genetic background nor progressive deterioration in renal function; thus, the differential diagnosis of URCD from ADPKD is important. Only a few cases of URCD have been reported. This study reports two cases of URCD in adults together with a literature review. We identified these two cases using abdominal computerized tomography and family screening with renal ultrasonography.

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