SPONTANEOUS PERFORATION OF INFANTILE CHOLEDOCHAL CYST - A RARE PRESENTATION.

Journal Title: International Journal of Advanced Research (IJAR) - Year 2019, Vol 7, Issue 8

Abstract

Spontaneous perforation is a rare complication of infantile choledochal cyst. We present a case of infantile choledochal cyst in a new born, which presented with abdominal distension, jaundice and acholic stools from 20 days of life. On evaluation was found to have focal dilatation of common bile duct and free fluid with septations. The infant underwent laparotomy and excision of the choledochal cyst followed by a Roux-en-y hepatico jejunostomy. It is important to follow up new born with choledochal cyst and intervene early with definitive management, for better outcome.

Authors and Affiliations

Muthukumaran J , Vembar D , Sam Joel M.

Keywords

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  • EP ID EP634251
  • DOI 10.21474/IJAR01/9591
  • Views 71
  • Downloads 0

How To Cite

Muthukumaran J, Vembar D, Sam Joel M. (2019). SPONTANEOUS PERFORATION OF INFANTILE CHOLEDOCHAL CYST - A RARE PRESENTATION.. International Journal of Advanced Research (IJAR), 7(8), 1040-1042. https://europub.co.uk/articles/-A-634251