Resumen

ARTIS, María T; BARRIOS ALICE, Alice  y  SOCORRO, Grace. Abdominal pain and recurrent jaundice as demonstration clinic in a child with primary sclerosing cholangitis . Gen [online]. 2012, vol.66, n.2, pp.124-129. ISSN 2477-975X.

Primary sclerosing cholangitis is a disease progressive hepatobiliary characterized by chronic inflammation with bile duct intra periductal fibrosis and extrahepatic that produce widespread biliary tract constrictions and ectasia. The case of a male school of 12 years of age who start current illness from 5 years of age when he presented recurrent abdominal pain located in the epigastrium and mesogastrio, mild to moderate intensity, cramping occurs. From the age of 8 was annexed on skin and mucosa, icteric dye with urine colored intermittently. To 10 years of age, 16/06/2008, abdominal pain increases in intensity accompanied of nausea, he received treatment with sucralfate and ranitidine without improvement for what 06 19, 2008 hospitalized. Laboratory tests which reported elevation of transaminases, alkaline phosphatase and gamma-glutamyl transpeptidase was carried out. Abdominal CT signs suggestive of cholangitis by what took place some virus serology hepatotropic, Magnetic Resonance Cholangiography and then liver biopsy corroborating the diagnosis of primary sclerosing cholangitis. Although is a disease common in the adult cholestatic should be taken into account in children to make an early diagnosis and subsequent follow-up.

Palabras clave : Cholangitis; Sclerosing; Primary; Child.