Abstract:Aplastic anemia is a rare blood disease characterized by the destruction of the hematopoietic stem cells (HSC) in the bone marrow that, in the majority of cases, is caused by an autoimmune reaction. Patients with aplastic anemia are treated with immunosuppressive drugs and some of them, especially younger individuals with a donor available, can be successfully treated with hematopoietic stem cell transplantation (HSCT). We report here a rare case of post-transplant lymphoproliferative disorder (PTLD) associate… Show more
“…The rare condition of post-transplant lymphoproliferative disorder (PTLD) linked with EBV reactivation was detected in a case report on a female patient (30-year-old) who experienced allogeneic hematopoietic stem cell transplantation (HSCT) for acute aplastic anemia. A full clinical recovery with no signs of EBV reactivation and neurotoxicity was attained by treating the patient with three cycles of a high dose of methotrexate along with rituximab [11].…”
Infection with certain types of deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) viruses, known as tumor viruses or oncogenic viruses, can lead to cancer [...]
“…The rare condition of post-transplant lymphoproliferative disorder (PTLD) linked with EBV reactivation was detected in a case report on a female patient (30-year-old) who experienced allogeneic hematopoietic stem cell transplantation (HSCT) for acute aplastic anemia. A full clinical recovery with no signs of EBV reactivation and neurotoxicity was attained by treating the patient with three cycles of a high dose of methotrexate along with rituximab [11].…”
Infection with certain types of deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) viruses, known as tumor viruses or oncogenic viruses, can lead to cancer [...]
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