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Percutaneous transhepatic cholangiodrainage as a bridging procedure for liver transplantation in biliary atresia

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Abstract

This case report describes a patient with an unusual type of biliary atresia that precluded the Kasai operation but who survived for 2 years and 6 months with percutaneous transhepatic cholangiodrainage (PTCD) and was successfully bridged to liver transplantation. PTCD is recommended when there is no bile excretion after a Kasai operation.

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References

  1. Ken Kimura, Shinji Hashimoto, Eiji Nishijima (1980) Percutaneous transhepatic cholangiodrainage after hepatic protenterosotmy for biliary atresia. J Pediatr Surg 15: 811–816

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  2. Ken Kimura, Toshihiro Muraji, Katsuhiko Ueoka (1987) Percutaneous transhepatic cholangiodrainage for patients with biliary atresia. Biliary Atresia. Professional Postgraduate Services. Ryoji Ohi. pp 211–215

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Muraji, T., Lynch, S., Ong, T. et al. Percutaneous transhepatic cholangiodrainage as a bridging procedure for liver transplantation in biliary atresia. Pediatr Surg Int 5, 361–363 (1990). https://doi.org/10.1007/BF00177107

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  • DOI: https://doi.org/10.1007/BF00177107

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