Rapid progression of acquired amegakaryocytic thrombocytopenia to myelodysplastic syndrome: Case report

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dc.authorscopusid8842895600
dc.authorscopusid7004568106
dc.authorscopusid57225396792
dc.authorscopusid12546230000
dc.authorscopusid12544841200
dc.authorscopusid6603472555
dc.authorscopusid56264100700
dc.contributor.authorErkurt M.A.
dc.contributor.authorKaya E.
dc.contributor.authorBaran M.
dc.contributor.authorYitmen E.
dc.contributor.authorŞenel S.
dc.contributor.authorKuku I.
dc.contributor.authorAydo?du I.
dc.date.accessioned2024-08-04T20:01:09Z
dc.date.available2024-08-04T20:01:09Z
dc.date.issued2005
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAcquired amegakaryocytic thrombocytopenia (AAT) is a rare disease characterized by severe thrombocytopenia due to selective reduction or absence of megakaryocytes in the bone marrow. More commonly, patients with AAT have additional hematologic abnormalities such as macrocytosis or dyserythropoiesis, abnormalities which may predict progression to aplastic anemia or myelodysplasia. A 52-year-old female was admitted to hospital with mucosal and gingival bleeding. Megakaryocytes were not seen on the bone marrow aspiration and biopsy. AAT was diagnosed. Although she was treated with immunosuppressive therapy including prednisolone and cyclosporine, her disease progressed to myelodysplastic syndrome. She died at the third month of diagnosis because of cerebral bleeding.en_US
dc.identifier.endpage208en_US
dc.identifier.issn1300-7777
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-33144462959en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage205en_US
dc.identifier.urihttps://hdl.handle.net/11616/91296
dc.identifier.volume22en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Haematologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcquired amegakaryocytic thrombocytopeniaen_US
dc.subjectMyelodysplastic syndromeen_US
dc.titleRapid progression of acquired amegakaryocytic thrombocytopenia to myelodysplastic syndrome: Case reporten_US
dc.typeArticleen_US

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