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All Journal The Indonesian Journal of Gastroenterology, Hepatology and Digestive Endoscopy
Jeanne Winarta
Division of Gastroentero-hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
Medicine & Pharmacology

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Polycystic Liver Disease: A Case Report Randy Adiwinata; Natalin Allorerung; Jonathan Arifputra; Andrea Livina; Pearla Lasut; Bradley Jimmy Waleleng; Fandy Gosal; Luciana Rotty; Jeanne Winarta; Andrew Waleleng; Michael Tendean
The Indonesian Journal of Gastroenterology, Hepatology, and Digestive Endoscopy Vol 22, No 2 (2021): VOLUME 22, NUMBER 2, August 2021
Publisher : The Indonesian Society for Digestive Endoscopy

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (883.669 KB) | DOI: 10.24871/2222021159-163

Abstract

Polycystic liver disease is characterized by multiple cystic lesions on the liver. Liver cysts are typically incidental findings, with occasional complications including cyst hemorrhage, infection and rupture. Polycystic liver disease may be part of autosomal dominant polycystic liver disease (ADPLD). Autosomal dominant polycystic liver disease is considered rare autosomal dominant disease, with prevalence of 1/100,000-1,000,000. Without family history of polycystic liver disease, ADPLD is defined as the presence of more than 20 liver cysts with no renal cysts, however up to third of ADPLD may have small number of renal cysts without kidney function impairment. This case of a 73-year-old woman with symptomatic polycystic liver disease, and we performed cyst fenestration-deroofing via laparoscopic.
Co-Authors Andrea Livina Andrew Waleleng Bradley Jimmy Waleleng Fandy Gosal Jonathan Arifputra Luciana Rotty Michael Tendean Natalin Allorerung Pearla Lasut Randy Adiwinata