Transcatheter arterial embolization therapy for a massive polycystic liver in autosomal dominant polycystic kidney disease patients

Polycystic liver is the most common extra-renal manifestation associated with autosomal dominant polycystic kidney disease (ADPKD), comprising up to 80% of all features. Patients with polycystic liver often suffer from abdominal discomfort, dyspepsia, or dyspnea; however, there have been few ways to...

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Published inJournal of Korean medical science Vol. 24; no. 1; pp. 57 - 61
Main Authors Park, Hayne Cho, Kim, Chi Weon, Ro, Han, Moon, Ju-Young, Oh, Kook-Hwan, Kim, Yonsu, Lee, Jung Sang, Yin, Yong Hu, Jae, Hwan Jun, Chung, Jin Wook, Ahn, Curie, Hwang, Young-Hwan
Format Journal Article
LanguageEnglish
Published Korea (South) The Korean Academy of Medical Sciences 01.02.2009
대한의학회
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Summary:Polycystic liver is the most common extra-renal manifestation associated with autosomal dominant polycystic kidney disease (ADPKD), comprising up to 80% of all features. Patients with polycystic liver often suffer from abdominal discomfort, dyspepsia, or dyspnea; however, there have been few ways to relieve their symptoms effectively and safely. Therefore, we tried transcatheter arterial embolization (TAE), which has been used in treating hepatocellular carcinoma. We enrolled four patients with ADPKD in Seoul National University Hospital, suffering from enlarged polycystic liver. We embolized the hepatic arteries supplying the dominant hepatic segments replaced by cysts using polyvinyl alcohol particles and micro-coils. The patients were evaluated 12 months after embolization for the change in both liver and cyst volumes. Among four patients, one patient was lost in follow up and 3 patients were included in the analysis. Both liver (33%; 10%) and cyst volume (47.7%; 11.4%) substantially decreased in two patients. Common adverse events were fever, epigastric pain, nausea, and vomiting. We suggest that TAE is effective and safe in treating symptomatic polycystic liver in selected ADPKD patients.
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G704-000345.2009.24.1.008
http://kmbase.medric.or.kr/Main.aspx?d=KMBASE&m=VIEW&i=0191120090240010057
ISSN:1011-8934
1598-6357
DOI:10.3346/jkms.2009.24.1.57