Abstract
Pancreatic heterotopia is generally asymptomatic and occurs in gut-related sites. An antenatally detected subhepatic cyst was finally diagnosed to be a congenital biliary cystic dilatation (without a caudal duodenal communication) with macroscopic Heinrich Type 2 pancreatic heterotopia. The embryogenesis and pathology of the malformation are discussed.
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Kattepura, S., Nanjegowda, N.B., Babu, M.K. et al. Macroscopic pancreatic heterotopia on a congenital biliary dilatation. Pediatr Surg Int 26, 847–849 (2010). https://doi.org/10.1007/s00383-009-2499-3
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DOI: https://doi.org/10.1007/s00383-009-2499-3