2015
DOI: 10.1159/000375117
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Peritoneal Recurrence of Initially Controlled Hepatocellular Carcinoma after Living Donor Liver Transplantation

Abstract: It is well known that the presence of end-stage liver disease increases the risk of developing hepatocellular carcinoma (HCC). Liver transplantation (LT) for patients within the Milan criteria has become a standard treatment for HCC in most developed centers worldwide. However, a major cause of death in cirrhotic patients with HCC after transplantation is tumor recurrence, including peritoneal recurrences, which develops rarely but presents a significant problem with regard to their management. Our experience … Show more

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Cited by 3 publications
(2 citation statements)
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“…The patient received LDLT 11 months after the bridging period, while downstaging of HCC with three cycles of TACE and no recurrence was observed 20 months after the operation. Data and outcomes of previous studies on LT after HCC rupture and our present study results are described in Table 3 ( 13 15 , 20 ). The present study contributes significantly to the field compared to previous case reports because this study had multiple cases treated with a similar protocol at a single center and was limited to patients who received a liver from a living donor.…”
Section: Discussionmentioning
confidence: 92%
“…The patient received LDLT 11 months after the bridging period, while downstaging of HCC with three cycles of TACE and no recurrence was observed 20 months after the operation. Data and outcomes of previous studies on LT after HCC rupture and our present study results are described in Table 3 ( 13 15 , 20 ). The present study contributes significantly to the field compared to previous case reports because this study had multiple cases treated with a similar protocol at a single center and was limited to patients who received a liver from a living donor.…”
Section: Discussionmentioning
confidence: 92%
“…[3][4][5] Hepatocellular carcinoma recurrence after LDLT has long been recognized as a reason for high patient mortality. [6][7][8] In addition, the risk of HBV reinfection after LDLT can be minimized by efficient combinations of therapeutic prophylactic agents. [9][10][11][12][13] However, emergence of drug mutations, such as emergence of the HBV polymerase gene locus known as tyrosine-methionine-aspartate-aspartate (YMDD), can result in resistance to the commonly used HBV prophylactic agents, including the purine nucleoside analog reverse-transcriptase inhibitor lamivudine.…”
Section: Introductionmentioning
confidence: 99%