Abstract
Biliary atresia remains one of the most intractable gastrointestinal surgical diseases in infancy. The introduction of liver transplantation (LTx) has revolutionized the protocols for the treatment of this condition, hepatic portoenterostomy (the Kasai procedure) is still the first-line surgical treatment.Early diagnosis, correct surgical techniques of the Kasai procedure, careful long-term follow-up, early treatment for complications, and appropriate indication of LTx if needed are keys to best management of patients with biliary atresia.
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© 2019 Springer-Verlag GmbH Germany, part of Springer Nature
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Nio, M., Sasaki, H., Tanaka, H., Ohi, R. (2019). Biliary Atresia. In: Puri, P., Höllwarth, M. (eds) Pediatric Surgery. Springer Surgery Atlas Series. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-56282-6_41
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DOI: https://doi.org/10.1007/978-3-662-56282-6_41
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