Abstract
Four infants in whom choledochal cyst was diagnosed by maternal ultrasound examinations are reviewed. The infants, from different institutions, represent a spectrum with regard to clinical presentation and subsequent course. They show that choledochal cyst can develop at different stages of gestation and is often not associated with biliary obstruction or biliary atresia. Definitive surgery can be safely performed in the neonatal period and is the treatment of choice. Follow-up data indicate that despite marked differences in the initial severity of their hepatic parenchymal disease, all four infants have done well in their early years, with essentially normal liver function. These unique patients provide insights into the possible etiology and pathophysiology of choledochal cyst and suggest guidlines for future evaluation and management of such infants.
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Marchildon, M.B. Antenatal diagnosis of choledochal cyst: the first four cases. Pediatr Surg Int 3, 431–436 (1988). https://doi.org/10.1007/BF00173461
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DOI: https://doi.org/10.1007/BF00173461