De novo cholangiocarcinoma after liver transplantation in a pediatric patient

Nandini Channabasappa; Sarah Johnson-Welch; Naveen Mittal

doi:10.1111/j.1399-3046.2009.01220.x

De novo cholangiocarcinoma after liver transplantation in a pediatric patient

Nandini Channabasappa
, Sarah Johnson-Welch
, Naveen Mittal

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

To date, no child has been reported to develop de novo CCA after liver transplantation although patients with transplants have a significantly higher risk of malignancy than the general population. CCA is extremely rare in the pediatric age group, seen mostly in patients with a history of choledochal cysts, Caroli's disease, or PSC. We report the first case of pediatric de novo CCA in the liver allograft 12 yr after liver transplantation.

Original language	English (US)
Pages (from-to)	E110-E114
Journal	Pediatric Transplantation
Volume	14
Issue number	8
DOIs	https://doi.org/10.1111/j.1399-3046.2009.01220.x
State	Published - Dec 2010
Externally published	Yes

Keywords

cholangiocarcinoma
de novo cancer
liver transplant

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Transplantation

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10.1111/j.1399-3046.2009.01220.x

Cite this

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title = "De novo cholangiocarcinoma after liver transplantation in a pediatric patient",

abstract = "To date, no child has been reported to develop de novo CCA after liver transplantation although patients with transplants have a significantly higher risk of malignancy than the general population. CCA is extremely rare in the pediatric age group, seen mostly in patients with a history of choledochal cysts, Caroli's disease, or PSC. We report the first case of pediatric de novo CCA in the liver allograft 12 yr after liver transplantation.",

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AU - Johnson-Welch, Sarah

AU - Mittal, Naveen

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AB - To date, no child has been reported to develop de novo CCA after liver transplantation although patients with transplants have a significantly higher risk of malignancy than the general population. CCA is extremely rare in the pediatric age group, seen mostly in patients with a history of choledochal cysts, Caroli's disease, or PSC. We report the first case of pediatric de novo CCA in the liver allograft 12 yr after liver transplantation.

KW - cholangiocarcinoma

KW - de novo cancer

KW - liver transplant

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De novo cholangiocarcinoma after liver transplantation in a pediatric patient

Abstract

Keywords

ASJC Scopus subject areas

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