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Choledochal cyst : a case report / Maria Angela P. Hernando.

Contributor(s): Language: english Publication details: Fairview, Quezon City Department of Child Heath, FEU-NRMF, 2009Description: tables; (in folder)Content type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
LOC classification:
  • CH 2009 0001
Summary: Abstract: A 1 year and 10 month old, female infant presented with abdominal enlargement for 9 months and jaundice for one month. Physical findings included generalized jaundice, abdominal enlargement and a firm, palpable mass on the right upper quadrant measuring 12cms x 7 cms. Patient underwent excision of choledochal cyst and hepaticoduodenostomy. The importance of constant follow up was explained to the parents. Choledochal cyst is a rare condition occurring in less than 1% of the population. It is a congenital dilatation of the hepatic and biliary ducts with 5 different types. Ultrasound is the initial imaging study of choice. Diagnosis was confirmed by upper abdominal CT scan. At present, surgery is the only mode of therapy for all forms of choledochal cysts.
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Includes appendices and bibliographical references.

Abstract: A 1 year and 10 month old, female infant presented with abdominal enlargement for 9 months and jaundice for one month. Physical findings included generalized jaundice, abdominal enlargement and a firm, palpable mass on the right upper quadrant measuring 12cms x 7 cms. Patient underwent excision of choledochal cyst and hepaticoduodenostomy. The importance of constant follow up was explained to the parents. Choledochal cyst is a rare condition occurring in less than 1% of the population. It is a congenital dilatation of the hepatic and biliary ducts with 5 different types. Ultrasound is the initial imaging study of choice. Diagnosis was confirmed by upper abdominal CT scan. At present, surgery is the only mode of therapy for all forms of choledochal cysts.

Research - Department of Child Health

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