Bibliographic Details
| Title: |
Polycystic Liver Disease: A Case Report. |
| Authors: |
Adiwinata, Randy, Allorerung, Natalin, Arifputra, Jonathan, Livina, Andrea, Lasut, Pearla, Waleleng, Bradley Jimmy, Gosal, Fandy, Rotty, Luciana, Winarta, Jeanne, Waleleng, Andrew, Tendean, Michael |
| Source: |
Indonesian Journal of Gastroenterology, Hepatology & Digestive Endoscopy; Aug2021, Vol. 22 Issue 2, p159-163, 5p |
| Subject Terms: |
LIVER diseases, CYSTIC kidney disease, KIDNEY physiology |
| Abstract (English): |
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. [ABSTRACT FROM AUTHOR] |
| Abstract (Indonesian): |
Penyakit hati polikistik dikarakteristikan dengan adanya lesi kista multipel pada hati. Kista hati seringkali hanya merupakan temuan insidentil, dengan potensi komplikasi yang jarang yaitu berupa perdarahan, infeksi, dan ruptur kista. Penyakit hati polikistik dapat merupakan bagian dari penyakit hati polikistik yang bersifat autosomal dominan. Penyakit hati polikistik autosomal dominan merupakan suatu penyakit yang jarang ditemukan dengan prevalensi dilaporkan antara 1/100.000 hingga 1/1.000.000 kasus. Pada pasien tanpa riwayat keturunan penyakit polikistik, penyakit hati polikistik autosomal dominan didefinisikan sebagai ditemukannya lebih dari 20 kista hati dengan tanpa adanya kista ginjal, akan tetapi pada sepertiga kasus dapat ditemukan kista ginjal dalam jumlah sedikit tanpa adanya perubahan fungsi ginjal. Pada laporan kasus ini dilaporkan seorang wanita berusia 73 tahun dengan penyakit polikistik hati simptomatik, dan pada pasien dilakukan tindakan fenestrasi dan deroofing kista secara laparoskopik. [ABSTRACT FROM AUTHOR] |
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Copyright of Indonesian Journal of Gastroenterology, Hepatology & Digestive Endoscopy is the property of Indonesian Society of Gastroenterology/Assoc for the Study of the Liver/Soc. for Digestive Endoscopy and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
| Database: |
Complementary Index |
