Biliary cystadenoma: Rare variant of intrahepatic cystic disease

Citation
Aw. Knott et al., Biliary cystadenoma: Rare variant of intrahepatic cystic disease, SOUTH MED J, 93(7), 2000, pp. 698-702
Citations number
36
Categorie Soggetti
General & Internal Medicine
Journal title
SOUTHERN MEDICAL JOURNAL
ISSN journal
00384348 → ACNP
Volume
93
Issue
7
Year of publication
2000
Pages
698 - 702
Database
ISI
SICI code
0038-4348(200007)93:7<698:BCRVOI>2.0.ZU;2-R
Abstract
Intrahepatic nonparasitic cystic disease is rare and may be of congenital o r neoplastic origin, The most frequent symptoms and signs are nonspecific a nd include pain, nausea, fullness, increased girth, and palpable mass. Inte rventional therapy is reserved for symptomatic patients, which usually corr esponds to cysts >5 cm in diameter, Retrospective analysis revealed 26 case s of intrahepatic cystic disease over 15 years at our institution, We discu ss the case of a patient who had bilobular biliary cystadenomatous disease, a rare, benign variant of intrahepatic nonparasitic cystic disease.