| Literature DB >> 24868329 |
Vikrant Sood1, Rajeev Khanna1, Seema Alam1, Dinesh Rawat1, Shorav Bhatnagar1, Archana Rastogi1.
Abstract
An eleven-year-old clinically dysmorphic and developmentally retarded male child presenting with complaints of 5 episodes of recurrent cholestatic jaundice since 3 years of age was evaluated. Imaging revealed features consistent with congenital extrahepatic portocaval shunt (Abernethy type 1b), multiple regenerative liver nodules and intrahepatic biliary radical dilatation. The presence of ductal paucity and trisomy 8 were confirmed on liver biopsy and karyotyping. The explanation for unusual and previously unreported features in the present case has been proposed.Entities:
Keywords: Congenital extrahepatic portocaval shunt; Ductal paucity; Trisomy 8; Warkany syndrome
Year: 2014 PMID: 24868329 PMCID: PMC4033293 DOI: 10.4254/wjh.v6.i5.358
Source DB: PubMed Journal: World J Hepatol