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Int J Hematol ; 118(2): 299-302, 2023 Aug.
Article in English | MEDLINE | ID: mdl-36802325

ABSTRACT

Autoimmune neutropenia (AIN) is an exceptionally rare condition that occurs after liver transplantation. Here, we report an adult case of refractory AIN 3.5 years after liver transplantation. A 59-year-old man who underwent brain-dead donor liver transplantation in August 2018 developed rapid neutropenia (0.07 × 109/L) in December 2021. The patient was diagnosed with AIN based on positivity for anti-human neutrophil antigen-1a antibody. There was no response to granulocyte colony-stimulating factor (G-CSF), prednisolone, or rituximab, and intravenous immunoglobulin (IVIg) therapy induced only a temporary recovery in neutrophil count. The patient continued to have a low neutrophil count for several months. However, the response to IVIg and G-CSF improved after the post-transplant immunosuppressant was changed from tacrolimus to cyclosporine. Post-transplant AIN has many unknown aspects. Tacrolimus-induced immunomodulation and graft-associated alloimmunity may be involved in its pathogenesis. Further studies are needed to elucidate the underlying mechanisms and explore new treatment options.


Subject(s)
Liver Transplantation , Myelodysplastic Syndromes , Neutropenia , Male , Humans , Adult , Middle Aged , Liver Transplantation/adverse effects , Immunoglobulins, Intravenous , Tacrolimus/adverse effects , Living Donors , Neutropenia/etiology , Neutropenia/chemically induced , Granulocyte Colony-Stimulating Factor/adverse effects
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