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2016, Number 5

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Gac Med Mex 2016; 152 (5)

Ictericia secundaria a obstrucción de vía biliar por enfermedad hepática poliquística: reporte de un caso

Ramírez-Guillén F, Rosas-Carrasco O, Cajuste-Sequeira F, Barriga-Pérez GB, Cabanillas-Morel A, Rosales-Salinas AE, Peña-Pérez JA

Language: Spanish
References: 17
Page: 715-718
PDF size: 237.31 Kb.


ABSTRACT

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.


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