Literature DB >> 24443335

Polycystic liver disease.

Rodrigo Nazário Leão1, Raquel Salustio, José Vaz Ribeiro.   

Abstract

A widespread use of ultrasound (US) examination is contributing to an increase in the diagnosis of renal and hepatic cysts. However, the vast majority of these lesions are benign with an indolent course during the patient's lifespan. Adult polycystic kidney disease (APKD) is one of the most common diagnosed entities. APKD is a genetic disease defined by the presence of multiple kidney cysts, occasionally accompanied by hepatic cysts. The presence of hepatic cysts sparing kidneys is very rare and thereby must be assumed as a different clinical entity. This article describes a case of an exuberant hepatomegaly due to the presence of isolated multiple hepatic cysts without renal involvement.

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Mesh:

Year:  2014        PMID: 24443335      PMCID: PMC3902511          DOI: 10.1136/bcr-2013-202003

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  12 in total

Review 1.  Medical and surgical treatment options for polycystic liver disease.

Authors:  Joost P H Drenth; Melissa Chrispijn; David M Nagorney; Patrick S Kamath; Vicente E Torres
Journal:  Hepatology       Date:  2010-12       Impact factor: 17.425

2.  Randomized clinical trial of long-acting somatostatin for autosomal dominant polycystic kidney and liver disease.

Authors:  Marie C Hogan; Tetyana V Masyuk; Linda J Page; Vickie J Kubly; Eric J Bergstralh; Xujian Li; Bohyun Kim; Bernard F King; James Glockner; David R Holmes; Sandro Rossetti; Peter C Harris; Nicholas F LaRusso; Vicente E Torres
Journal:  J Am Soc Nephrol       Date:  2010-04-29       Impact factor: 10.121

Review 3.  Isolated polycystic liver disease.

Authors:  Qi Qian
Journal:  Adv Chronic Kidney Dis       Date:  2010-03       Impact factor: 3.620

Review 4.  New advances in evaluation and management of patients with polycystic liver disease.

Authors:  Hays L Arnold; Stephen A Harrison
Journal:  Am J Gastroenterol       Date:  2005-11       Impact factor: 10.864

Review 5.  Systematic review: the pathophysiology and management of polycystic liver disease.

Authors:  F Temmerman; L Missiaen; B Bammens; W Laleman; D Cassiman; C Verslype; J van Pelt; F Nevens
Journal:  Aliment Pharmacol Ther       Date:  2011-07-26       Impact factor: 8.171

6.  Volume progression in polycystic kidney disease.

Authors:  Jared J Grantham; Vicente E Torres; Arlene B Chapman; Lisa M Guay-Woodford; Kyongtae T Bae; Bernard F King; Louis H Wetzel; Deborah A Baumgarten; Phillip J Kenney; Peter C Harris; Saulo Klahr; William M Bennett; Gladys N Hirschman; Catherine M Meyers; Xiaoling Zhang; Fang Zhu; John P Miller
Journal:  N Engl J Med       Date:  2006-05-18       Impact factor: 91.245

7.  Carbohydrate antigen 19-9 is extremely elevated in polycystic liver disease.

Authors:  Esmé Waanders; Loes van Keimpema; Johannes T Brouwer; Martijn G H van Oijen; Raymond Aerts; Fred C G J Sweep; Frederik Nevens; Joost P H Drenth
Journal:  Liver Int       Date:  2009-06-03       Impact factor: 5.828

8.  Laparoscopic management of benign liver diseases: where are we?

Authors:  Jean-François Gigot; Catherine Hubert; Radu Banice; Michael L Kendrick
Journal:  HPB (Oxford)       Date:  2004       Impact factor: 3.647

Review 9.  Polycystic liver disease: a clinical review.

Authors:  Natasha Chandok
Journal:  Ann Hepatol       Date:  2012 Nov-Dec       Impact factor: 2.400

10.  Magnetic resonance imaging evaluation of hepatic cysts in early autosomal-dominant polycystic kidney disease: the Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease cohort.

Authors:  Kyongtae T Bae; Fang Zhu; Arlene B Chapman; Vicente E Torres; Jared J Grantham; Lisa M Guay-Woodford; Deborah A Baumgarten; Bernard F King; Louis H Wetzel; Philip J Kenney; Marijn E Brummer; William M Bennett; Saulo Klahr; Catherine M Meyers; Xiaoling Zhang; Paul A Thompson; J Philip Miller
Journal:  Clin J Am Soc Nephrol       Date:  2005-10-26       Impact factor: 8.237

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