Literature DB >> 25123318

Increasing occurrence of choledochal malformations in children: a single-center 37-year experience from Finland.

Maria Hukkinen1, Antti Koivusalo, Harry Lindahl, Risto Rintala, Mikko P Pakarinen.   

Abstract

OBJECTIVE: Few reports on choledochal malformations (CMs) in European populations exist.
MATERIALS AND METHODS: The medical records of pediatric CM patients managed in our nationwide referral center for pediatric hepatobiliary surgery between 1976 and 2013 (n = 38; 71% females) were reviewed.
RESULTS: Over follow-up time, the relative proportion of fusiform CMs increased significantly (p = 0.007) and the estimated total incidence rose from 1:128,000 to 1:38,000 (p = 0.017). Cystic CMs (42%) presented at younger age than fusiform CMs (47%) (0.8 vs. 4.6 years, p = 0.001). Two-thirds had abdominal pain and half were cholestatic at presentation. Pancreatitis had occurred in 16%. In addition to ultrasound, 71% underwent magnetic resonance cholangiopancreatography and 39% underwent endoscopic retrograde cholangiopancreatography. Median CM dilatation was 15 (10-28) mm and a 12 (9-13) mm long common pancreaticobiliary channel was confirmed in 61%, increasingly during recent years. Intrahepatic biliary tree was dilated in 19%, whereas main ducts were dilated in 50%. Apart from two operated in the 1970s and one with choledochocele, patients underwent resection of extrahepatic bile ducts with Roux-en-Y hepaticojejunostomy at age of 4.2 (0.8-9.2) years. Postoperative bile leakage and hemorrhage required reoperations in two. At last follow-up 4.8 (1.3-13.2) years postoperatively, none had dilated intrahepatic biliary ducts or elevated plasma bilirubin (5 [3-7] µmol/l). Single cholangitis episodes had occurred in two, whereas others were asymptomatic.
CONCLUSION: CM incidence has increased significantly in Finland, being currently over threefold higher than previous estimates in the Western world would suggest. Removal of the extrahepatic biliary tree with hepaticojejunostomy for type I and IV CMs yielded excellent results.

Entities:  

Keywords:  Choledochal cysts; choledochal malformations

Mesh:

Year:  2014        PMID: 25123318     DOI: 10.3109/00365521.2014.946084

Source DB:  PubMed          Journal:  Scand J Gastroenterol        ISSN: 0036-5521            Impact factor:   2.423


  3 in total

Review 1.  Laparoscopic management of choledochal cysts: is a keyhole view missing the big picture?

Authors:  Mark D Stringer
Journal:  Pediatr Surg Int       Date:  2017-04-19       Impact factor: 1.827

2.  Choledochal malformation: terminology and aetiology.

Authors:  Filippo Parolini; Mark Davenport
Journal:  Pediatr Surg Int       Date:  2017-11-13       Impact factor: 1.827

3.  De novo somatic mutations and KRAS amplification are associated with cholangiocarcinoma in a patient with a history of choledochal cyst.

Authors:  Marisa E Schwab; Hanbing Song; Aras Mattis; Andrew Phelps; Lan T Vu; Franklin W Huang; Amar Nijagal
Journal:  J Pediatr Surg       Date:  2020-03-24       Impact factor: 2.545

  3 in total

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