Long-term follow-up of hepatitis-associated aplastic anaemia

Prognosis of hepatitis-associated aplastic anaemia (HAAA) was improved with haematopoietic stem cell transplantation (HSCT) and immunosuppression, but the long-term outcome remains undefined. Case 1: a girl aged 3 years with acute liver failure (ALF) submitted to orthotopic liver transplantation (OLT) subsequently developed aplastic anaemia and HSCT from a compatible sibling was performed. Post-HSCT, the patient developed post-transplant lymphoproliferative disorder and rituximab was administered with good response. Fifteen years later, both grafts show good outcome. Case 2: a girl aged 10 years submitted to OLT due to ALF, developed pancytopenia 2 months later. Due to the absence of a human leucocyte antigen compatible donor, she was treated with ciclosporin and antithymocyte globulin with very good long-term outcome. These clinical cases suggest that, for patients with HAAA that underwent OLT, aggressive therapy with HSCT or immunosuppression may provide a benign long-term outcome.

[1]  A. Bertuch,et al.  Features of Hepatitis in Hepatitis-associated Aplastic Anemia: Clinical and Histopathologic Study , 2017, Journal of pediatric gastroenterology and nutrition.

[2]  G. Guariso,et al.  Inside and outside the liver: the challenge of hepatitis-associated aplastic anemia in children. , 2016, Minerva pediatrica.

[3]  T. Olson,et al.  Disrupted lymphocyte homeostasis in hepatitis‐associated acquired aplastic anemia is associated with short telomeres , 2016, American journal of hematology.

[4]  Jing-jing Zhu,et al.  Efficacy and safety of immunosuppressive therapy in the treatment of seronegative hepatitis associated aplastic anemia , 2014, Drug design, development and therapy.

[5]  Hong Liu,et al.  The Clinical and Immune Characteristics of Patients with Hepatitis-Associated Aplastic Anemia in China , 2014, PloS one.

[6]  N. Young,et al.  A Pilot Study Of Rituximab In Patients With Moderate Aplastic Anemia, Diamond-Blackfan Anemia and Pure Red Cell Aplasia , 2013 .

[7]  E. Yoshida,et al.  Recurrent idiopathic acute hepatitis-associated aplastic anemia/pancytopenia fourteen years after initial episode. , 2010, Annals of hepatology.

[8]  J. Passweg,et al.  Hepatitis‐associated aplastic anaemia: epidemiology and treatment results obtained in Europe. A report of The EBMT aplastic anaemia working party , 2010, British journal of haematology.

[9]  J. Gisbert,et al.  Systematic review: hepatitis‐associated aplastic anaemia – a syndrome associated with abnormal immunological function , 2009, Alimentary pharmacology & therapeutics.

[10]  Allen R. Chen,et al.  Treatment of hepatitis‐associated aplastic anemia with high‐dose cyclophosphamide , 2006, Pediatric blood & cancer.

[11]  Masuji Yamamoto,et al.  Antithymocyte globulin and cyclosporine for treatment of 44 children with hepatitis associated aplastic anemia , 2007, Haematologica.

[12]  A. Németh,et al.  Acquired aplastic anaemia in seven children with severe hepatitis with or without liver failure , 2007, Acta paediatrica.

[13]  P. B. Hansen,et al.  Aplastic anemia successfully treated with rituximab , 2005, American journal of hematology.

[14]  Y. Romero,et al.  HEPATITIS-ASSOCIATED APLASTIC ANEMIA AND ACUTE PARVOVIRUS B19 INFECTION: A REPORT OF TWO CASES AND A REVIEW OF THE LITERATURE , 1998, American Journal of Gastroenterology.

[15]  F. Bosch,et al.  Transient pancytopenia after non-A non-B non-C acute hepatitis preceding acute lymphoblastic leukemia. , 1998, Haematologica.

[16]  R. Storb,et al.  Hepatitis-associated aplastic anemia. , 1997, The New England journal of medicine.

[17]  N. Young,et al.  Prevalence of GBV‐C/HGV, a novel ‘hepatitis’ virus, in patients with aplastic anaemia , 1997, British journal of haematology.

[18]  P. Stock,et al.  Aplastic anemia complicating orthotopic liver transplantation for non-A, non-B hepatitis. , 1988, The New England journal of medicine.

[19]  E. Lorenz,et al.  [Panmyelopathy following epidemic hepatitis]. , 1955, Wiener medizinische Wochenschrift.