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dc.contributor.authorYiğit Kaya, Süreyya
dc.contributor.authorAşkın, Abdullah Emre
dc.contributor.authorBektaş, Şebnem
dc.contributor.authorÇakır, Aslı
dc.contributor.authorGökmen Sevindik, Ömür
dc.date.accessioned2023-05-24T07:42:19Z
dc.date.available2023-05-24T07:42:19Z
dc.date.issued2023en_US
dc.identifier.citationYiğit Kaya, S., Aşkın, A. E., Bektaş, Ş., Çakır, A. ve Gökmen Sevindik, Ö. (2023). Newly onset cytopenias not always indicate a relapsing AML after allogeneic HSCT, a case of non-destructive post transplant lymphoproliferative disorder. Leukemia Research Reports, 19. https://doi.org/10.1016/j.lrr.2023.100369en_US
dc.identifier.issn2213-0489
dc.identifier.urihttps://doi.org/10.1016/j.lrr.2023.100369
dc.identifier.urihttps://hdl.handle.net/20.500.12511/10965
dc.description.abstractAllogeneic hematopoietic stem cell transplantation (allo-HSCT) remains an effective option for the treatment of intermediate and high-risk Acute myeloid leukemia (AML). Post-transplant lymphoproliferative disorder (PTLD) is related to the intensity of post-transplant immunosuppression. Although Epstein-Barr virus (EBV) seropositivity and reactivation can be a major risk factor for PTLD. A few PTLDs could be EBV negative. There are a very limited number of PTLD cases following HSCT in patients with AML. We present a differential diagnosis of cytopenias after allo-HSCT. This is the first report of an AML patient developing bone marrow EBV-negative PTLD relatively late in their post-transplant course.en_US
dc.language.isoengen_US
dc.publisherElsevier Ltden_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAcute Myeloid Leukemia (AML)en_US
dc.subjectEpstein-Barr Virusen_US
dc.subjectPost Transplant Lymphoproliferative Disorderen_US
dc.subjectRituximaben_US
dc.titleNewly onset cytopenias not always indicate a relapsing AML after allogeneic HSCT, a case of non-destructive post transplant lymphoproliferative disorderen_US
dc.typearticleen_US
dc.relation.ispartofLeukemia Research Reportsen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Tıbbi Patoloji Ana Bilim Dalıen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0003-0128-6947en_US
dc.authorid0000-0001-9636-4113en_US
dc.identifier.volume19en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1016/j.lrr.2023.100369en_US
dc.institutionauthorYiğit Kaya, Süreyya
dc.institutionauthorAşkın, Abdullah Emre
dc.institutionauthorBektaş, Şebnem
dc.institutionauthorÇakır, Aslı
dc.institutionauthorGökmen Sevindik, Ömür
dc.identifier.wos001051640000001en_US
dc.identifier.scopus2-s2.0-85156144672en_US
dc.identifier.pmid37213444en_US
dc.identifier.scopusqualityQ3en_US


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