Infection of hepatic cysts in polycystic disease
β Scribed by Javier Abascal; Manuel Moya; Fernando Martin
- Publisher
- Springer
- Year
- 1984
- Tongue
- English
- Weight
- 127 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0364-2313
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π SIMILAR VOLUMES
Hepatic cysts are a major manifestation of autosomal dominant polycystic kidney disease. This study examined 239 autosomal dominant polycystic kidney disease patients and 189 unaffected family members to define the factors that influence the presence and severity of hepatic cysts. Autosomal dominant
Polycystic liver disease is a common manifestation of autosomal dominant polycystic kidney disease. However, factors that regulate hepatic cystogenesis have not been defined, and the effect of cyst formation on hepatic parenchymal mass has not been studied. We validated computed tomographic methods
Cyst fluid from a patient with polycystic liver disease was obtained by needle aspiration using ultrasound guidance. The constituents of the fluid resembled the "bile salt-independent" fraction of human bile and supports the hypothesis that such cysts are lined by a functioning, secretory bile duct