Rangsan Niramis MD*, Rajit Narumitsuthon MD**, Sukawat Watanatittan MD*, Maitree Anuntkosol MD*, Veera Buranakitjaroen MD*, Achariya Tongsin MD*, Varaporn Mahatharadol MD*, Suranetr Laorwong MD*
Affiliation : * Department of Surgery, Queen Sirikit National Institute of Child Health, College of Medicine, Rangsit University, Bangkok, Thailand ** Department of Surgery, Yala Hospital, Yala, Thailand
Background : Choledochal cysts (CDC) can become symptomatic at any age. Clinical features of infants and older children
are different and have been documented by many authors.
Objective : The aim of this report was to study the differences in clinical spectrum of CDC between the infants and children
treated at our hospital during a 17-year period.
Material and Method: A retrospective study was conducted of 160 patients with CDC treated at Queen Sirikit National
Institute of Child Health between 1996 and 2012. The patients were categorized into 2 groups based on age at clinical
presentation: an infantile group (up to one year old) and a childhood group (over one year old). Clinical characteristics of
patients in the infantile and childhood groups were compared with statistical analysis using the Chi-square and Fisher’s exact
test.
Results : Of the 160 patients with CDC, 48 cases (30%) were categorized in the infantile group and 112 cases (70%) in the
childhood group. Over three-quarters of the patients in the infantile group presented with jaundice and acholic stool, and this
incidence was significantly higher than in the childhood group (77% vs. 46.4%, p = 0.001 and 50% vs. 13.4%, p<0.001).
Abdominal pain was the most common symptom of patients in the childhood group, whereas it was noted in only a small
number of those in the infantile group (82.1% vs. 8.3%, p<0.001). Average amylase level in CDC content was markedly
elevated in the childhood group but much lower in the infantile group (43,630.5+90,234.5 vs. 79+189.9, p<0.001). Only type
I and type IV CDC as defined by Todani’s classification were found in our patients, and there were no statistical differences in
incidences of type I and type IV in the two groups (79.2% vs. 67.8% and 20.8% vs. 32.2% p>0.05). Neonates and infants with
CDC had a significantly higher risk of liver cirrhosis than did the childhood group (25% vs. 8%, p<0.001). However,
surviving patients with cirrhosis in both groups were doing well at least 3 years after surgical CDC excision.
Conclusion : Neonates and infants with CDC were more likely to present with jaundice and acholic stool, whereas older
children were more likely to present with abdominal pain. Amylase level in CDC content was markedly elevated in the
childhood group but at a much lower level in the infantile group. Neonates and infants with CDC tended to develop liver
cirrhosis earlier and more often than older children.
Keywords : Choledochal cyst, Infancy, Childhood, Todani’s classification
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