Polycystic Liver Disease: A Case Report

Authors

  • Randy Adiwinata Faculty of Medicine, Atmajaya Catholic University, Jakarta
  • Natalin Allorerung Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Jonathan Arifputra Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Andrea Livina Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Pearla Lasut Division of Hematology and Medical Oncology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Bradley Jimmy Waleleng Division of Gastroentero-hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Fandy Gosal Division of Gastroentero-hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Luciana Rotty Division of Gastroentero-hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Jeanne Winarta Division of Gastroentero-hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Andrew Waleleng Division of Gastroentero-hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado
  • Michael Tendean Division of Digestive Surgery, Department of Surgery, Faculty of Medicine, Universitas Sam Ratulangi/Prof. dr. RD Kandou Hospital, Manado

DOI:

https://doi.org/10.24871/2222021159-163

Keywords:

polycystic liver disease, autosomal dominant polycystic liver disease, cyst, treatment

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.

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Published

2021-09-27

How to Cite

Adiwinata, R., Allorerung, N., Arifputra, J., Livina, A., Lasut, P., Waleleng, B. J., … Tendean, M. (2021). Polycystic Liver Disease: A Case Report. The Indonesian Journal of Gastroenterology, Hepatology, and Digestive Endoscopy, 22(2), 159–163. https://doi.org/10.24871/2222021159-163

Issue

Vol. 22 No. 2 (2021): VOLUME 22, NUMBER 2, August 2021

Section

Case Reports

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