Literature DB >> 7377224

Liver cysts in patients with autosomal dominant polycystic kidney disease.

J Milutinovic, P J Fialkow, T G Rudd, L Y Agodoa, L A Phillips, J I Bryant.   

Abstract

Liver cysts were found in 46 (29 per cent) of 158 patients over 10 years of age with documented autosomal dominant-type polycystic kidney disease (PKD) from 62 unrelated families. Hepatic cysts were not found in any patient at risk for PKD in whom renal cysts were not detected. The prevalence of liver cysts increased with advancing age and with declining rate of glomerular filtration. Results of clinical and laboratory studies indicate that polycystic liver disease in patients with autosomal dominant-type PKD is a benign condition, rarely, if ever, causing impaired liver function or portal hypertension.

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Year:  1980        PMID: 7377224     DOI: 10.1016/0002-9343(80)90266-1

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  29 in total

1.  Polycystic liver disease with obstructive jaundice: treatment with ultrasound-guided cyst aspiration.

Authors:  M E Lerner; J E Roshkow; A Smithline; C Ng
Journal:  Gastrointest Radiol       Date:  1992

2.  A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2).

Authors:  B Veldhuisen; J J Saris; S de Haij; T Hayashi; D M Reynolds; T Mochizuki; R Elles; R Fossdal; N Bogdanova; M A van Dijk; E Coto; D Ravine; S Nørby; C Verellen-Dumoulin; M H Breuning; S Somlo; D J Peters
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

3.  Mutation detection in the repeated part of the PKD1 gene.

Authors:  J H Roelfsema; L Spruit; J J Saris; P Chang; Y Pirson; G J van Ommen; D J Peters; M H Breuning
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

4.  Bleeding oesophageal varices and hepatic dysfunction in adult polycystic kidney disease.

Authors:  P J Ratcliffe; S Reeders; J M Theaker
Journal:  Br Med J (Clin Res Ed)       Date:  1984-05-05

5.  Treatment of highly symptomatic polycystic liver disease. Preliminary experience with a combined hepatic resection-fenestration procedure.

Authors:  K D Newman; V E Torres; J Rakela; D M Nagorney
Journal:  Ann Surg       Date:  1990-07       Impact factor: 12.969

6.  Adult polycystic kidney disease: a disorder of connective tissue?

Authors:  Anwar Ul Haque; Ambreen Moatasim
Journal:  Int J Clin Exp Pathol       Date:  2008-01-01

7.  Aneurysms of coronary arteries in a patient with adult polycystic kidney disease: arteriosclerosis or involvement by the primary disease?

Authors:  M Christ; U Bechtel; S Schnaack; K Theisen; M Wehling
Journal:  Clin Investig       Date:  1993-02

8.  Treatment of polycystic liver disease with resection-fenestration and a new classification.

Authors:  Tuan-Jie Li; Hai-Bin Zhang; Jun-Hua Lu; Jun Zhao; Ning Yang; Guang-Shun Yang
Journal:  World J Gastroenterol       Date:  2008-08-28       Impact factor: 5.742

9.  Two cases of 5q deletions in patients with familial adenomatous polyposis: possible link with Caroli's disease.

Authors:  S V Hodgson; A S Coonar; P J Hanson; S Cottrell; P N Scriven; T Jones; P R Hawley; M L Wilkinson
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

10.  Downregulation of Ke 6, a novel gene encoded within the major histocompatibility complex, in murine polycystic kidney disease.

Authors:  N Aziz; M M Maxwell; B St Jacques; B M Brenner
Journal:  Mol Cell Biol       Date:  1993-03       Impact factor: 4.272

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