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. 2018 Jan 1;29(1):89–93. doi: 10.5152/tjg.2017.17089

Table 1.

Features of the patients who developed PTLD

Age at Tx, years Primary diagnosis Sex Oncologic diagnosis Diagnosis time, months Rejection EBV Immunosuppression Prognosis Pre-transplant EBV serology
6 Congenital hepatic fibrosis M PTLD 60 No Positive Tacrolimus Alive Positive
1 Biliary atresia F PTLD 36 No Negative Tacrolimus Alive Negative
11 Autoimmune hepatitis F PTLD 96 No Positive Cyclosporine Alive Positive
9 Fulminan Hepatitis A F PTLD 7 N Negative Tacrolimus Alive Positive
1 Bile acid synthesis defect F PTLD 24 Yes Negative Tacrolimus Alive Negative
3 PFIC M PTLD 12 No Negative Tacrolimus Died Negative
4 Biliary atresia F PTLD 7 No Negative Tacrolimus Alive Negative

PFIC: progressive familial intrahepatic cholestasis; PTLD: post-transplant lymphoproliferative disease; EBV: Epstein-Barr virus; M: male; F: female; Tx: transplantation