rejection is frequent after liver transplantation (LT). pathogenesis of acute cellular rejection (ACR) is attributable to recipient T cells; chronic rejection (CR) has a multifactorial pathogenesis. there is a striking increase in LT among women of reproductive age. thus, it is very important to understand how pregnancy can influence immune system and graft function. an 8-year-old female was liver transplanted in 1990 due to congenital atresia of biliary tract. patient started immunosuppressive therapy with cyclosporine and corticosteroids. a few weeks after transplantation, she had an acute rejection, treated with fourfold therapy. at 18 years old, a hepatic biopsy showed an immune-mediated chronic hepatitis. Immunosuppressive therapy was increased with azathioprine. In 2014 she had a baby and in 2015 she suspended immunosuppressive therapies. after thirty days, she attended Hospital for jaundice. histologic examination revealed both chronic hepatitis in cirrhotic evolution and acute rejection. patient was treated with steroids at high doses. cyclosporine was replaced with tacrolimus and everolimus, azathioprine was stopped. due to the clinical conditions, evaluation for a re-LT was started. In the following years, a progressive improvement in patient's general conditions and liver function was observed and, therefore, re-LT was not necessary. patient developed a sub-clinical CR and then ACR following suspension of immunosuppressive drugs. probably. pregnancy played a contribution in the development of liver damage mediated by the immune system. furthermore, patient completed pregnancy with compensated cirrhosis. anti-rejection therapy needs to be modulated constantly, obtaining a good clinical response.

Mitterhofer, A.p. (2021). Acute rejection on immune-mediated chronic rejection after liver transplantation. GAZZETTA MEDICA ITALIANA. ARCHIVIO PER LE SCIENZE MEDICHE, 180(4), 136-143 [10.23736/S0393-3660.19.04240-2].

Acute rejection on immune-mediated chronic rejection after liver transplantation

MITTERHOFER, ANNA PAOLA
2021-01-01

Abstract

rejection is frequent after liver transplantation (LT). pathogenesis of acute cellular rejection (ACR) is attributable to recipient T cells; chronic rejection (CR) has a multifactorial pathogenesis. there is a striking increase in LT among women of reproductive age. thus, it is very important to understand how pregnancy can influence immune system and graft function. an 8-year-old female was liver transplanted in 1990 due to congenital atresia of biliary tract. patient started immunosuppressive therapy with cyclosporine and corticosteroids. a few weeks after transplantation, she had an acute rejection, treated with fourfold therapy. at 18 years old, a hepatic biopsy showed an immune-mediated chronic hepatitis. Immunosuppressive therapy was increased with azathioprine. In 2014 she had a baby and in 2015 she suspended immunosuppressive therapies. after thirty days, she attended Hospital for jaundice. histologic examination revealed both chronic hepatitis in cirrhotic evolution and acute rejection. patient was treated with steroids at high doses. cyclosporine was replaced with tacrolimus and everolimus, azathioprine was stopped. due to the clinical conditions, evaluation for a re-LT was started. In the following years, a progressive improvement in patient's general conditions and liver function was observed and, therefore, re-LT was not necessary. patient developed a sub-clinical CR and then ACR following suspension of immunosuppressive drugs. probably. pregnancy played a contribution in the development of liver damage mediated by the immune system. furthermore, patient completed pregnancy with compensated cirrhosis. anti-rejection therapy needs to be modulated constantly, obtaining a good clinical response.
2021
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/14
Settore MED/12
English
Liver
Transplants
Therapy
Pregnancy
Mitterhofer, A.p. (2021). Acute rejection on immune-mediated chronic rejection after liver transplantation. GAZZETTA MEDICA ITALIANA. ARCHIVIO PER LE SCIENZE MEDICHE, 180(4), 136-143 [10.23736/S0393-3660.19.04240-2].
Mitterhofer, Ap
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/361290
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
social impact