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Gac Med Mex ; 152(5): 715-718, 2016.
Article in Spanish | MEDLINE | ID: mdl-27792710

ABSTRACT

Polycystic liver disease is an autosomal dominant disorder commonly associated with autosomal dominant polycystic kidney disease. It is a rare disease that usually occurs asymptomatically in 85% of cases and diagnosis is incidentally. We present the case of 57 years old woman with progressive pruritus and jaundice secondary to stenosis of the common hepatic duct and common bile by liver cyst, rare presentation which only has been documented in case reports: Deepak, et al., Wittig, et al. and Howard, et al.1-3.


Subject(s)
Cholestasis/complications , Cysts/complications , Jaundice, Obstructive/etiology , Liver Diseases/complications , Female , Hepatic Duct, Common , Humans , Middle Aged
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