2005
DOI: 10.1111/j.1442-2042.2005.01022.x
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Unilateral and segmental cystic disease of the kidney

Abstract: Unilateral and segmental cystic disease is a rare cystic disease of the kidney. Except for its unilaterality, it resembles autosomal dominant polycystic kidney disease on gross and histological examination. It also lacks genetic background and progressive deterioration of renal function. Only a small number of unilateral and segmental cystic disease of the kidney cases have been reported to date. The present case is a report of a 69-year-old man who had a large multicystic mass involving the lower and middle p… Show more

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Cited by 11 publications
(8 citation statements)
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“…Morphologically, it resembles ADPKD, which on the contrary shows progression towards renal failure and has extra-renal complications in the form of hepatic and pancreatic cysts, berry aneurysms, aortic dissections and bowel pathologies [9, 10]. In children, autosomal dominant polycystic kidney disease may manifest as localized cystic disease of kidney, but careful history along with radiological examinations of their parents leads to the diagnosis of autosomal dominant polycystic kidney disease.…”
Section: Discussionmentioning
confidence: 99%
“…Morphologically, it resembles ADPKD, which on the contrary shows progression towards renal failure and has extra-renal complications in the form of hepatic and pancreatic cysts, berry aneurysms, aortic dissections and bowel pathologies [9, 10]. In children, autosomal dominant polycystic kidney disease may manifest as localized cystic disease of kidney, but careful history along with radiological examinations of their parents leads to the diagnosis of autosomal dominant polycystic kidney disease.…”
Section: Discussionmentioning
confidence: 99%
“…However, we still have a limited understanding of segmental MCDK due to the limited number of studies and reports on this disease entity. 2,3,[7][8][9][10][11][12][13][14] Review of previous studies showed M A N U S C R I P T A C C E P T E D ACCEPTED MANUSCRIPT 2 that only 39 cases have been reported worldwide, and most were treated by routine surgical resection. Herein, we focused on conservative management of this relatively rare disease by investigation of involution, associated anomalies requiring surgery, and complications of segmental MCDK.…”
Section: Introductionmentioning
confidence: 97%
“…Unilateral renal cystic disease (URCD) is a rare disease characterized by cysts with various sizes in a diffusely enlarged kidney without forming a distinct encapsulated mass [1], [2], [3], [4], [5], [6]. Hwang et al reported that the prevalence of URCD in their center was 2.4% [1].…”
Section: Introductionmentioning
confidence: 99%
“…Hwang et al reported that the prevalence of URCD in their center was 2.4% [1]. The differential diagnoses of URCD are autosomal dominant polycystic disease (ADPKD), multilocular cystic renal neoplasms, cystic dysplasia, and multiple simple cysts [1], [5], [7], [8]. It is important to distinguish URCD from ADPKD due to their different outcome [1], [3], [6], [8], [9].…”
Section: Introductionmentioning
confidence: 99%