Evans syndrome: A case report

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dc.contributor.authorTaşkesen M.
dc.contributor.authorOkur N.
dc.contributor.authorOkur N.
dc.contributor.authorSöker M.
dc.date.accessioned2024-04-24T17:59:01Z
dc.date.available2024-04-24T17:59:01Z
dc.date.issued2009
dc.departmentDicle Üniversitesien_US
dc.description.abstractEvans syndrome is rare and characterized with autoimmun thrombocytopenia and hemolytic anemia. Etiology is unknown. The patients may apply with different clinical findings. Seven years old boy was refered for fever, abdominal pain and epistaxis. In physical examination pallor and hepatosplenomegaly were detected. In laboratory anemia, thrombocytopenia, insufficient of thrombocytes and hemolysis in periferic blood smear, high lactic dehydrogenase, low haptoglobulin, increased reticu-locyte count were found and Direct Coombs test were positive. Hypercellularity, increased erytroid series and megacar-yocytes were determined in bone marrow examination. Erythrocyte suspension and intravenous immunglobulin were used for treatment. In 12 days follow-up hemoglobine level and platelet count were in normal limits and patient was discharged succesfully. The patient had no symptoms and normal laboratory findings two months later. The aim of this case report is evaluation of clinical and laboratory features of Evans syndrome.en_US
dc.identifier.endpage45en_US
dc.identifier.issn1300-526X
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-64549139763en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage43en_US
dc.identifier.urihttps://hdl.handle.net/11468/24193
dc.identifier.volume24en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.relation.ispartofGoztepe Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChildhooden_US
dc.subjectHemolytic Anemiaen_US
dc.subjectThrombocytopeniaen_US
dc.titleEvans syndrome: A case reporten_US
dc.title.alternativeEvans sendromu: Bir vaka takdimien_US
dc.typeArticleen_US

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