Brusellaya Bagli Trombositopenik Purpura

dc.contributor.authorOzen, Metehan
dc.contributor.authorOzgen, Unsal
dc.contributor.authorGungor, Serdal
dc.date.accessioned2024-08-04T20:57:19Z
dc.date.available2024-08-04T20:57:19Z
dc.date.issued2009
dc.departmentİnönü Üniversitesien_US
dc.description.abstractBrucellar infections are still a major public health issue in Mediterranean countries. Brucellosis may cause hematological abnormalities, particularly cytopenias. Severe thrombocytopenia leading to mucosal bleeding and purpuric rash is relatively infrequent. We herewith present three patients who were admitted with mucosal bleeding and purpura, and were finally diagnosed as brucellosis. The severe isolated thrombocytopenia, purpuric rash and compatible bone marrow findings on admission suggested the presumed diagnosis of ITP in all cases. All three patients received different treatment regimens and finally recovered without complications. There is no consensus regarding the management of brucella-induced thrombocytopenic purpura in the literature. The hematological consequences of brucellosis should always be kept in mind in the differential diagnosis of isolated thrombocytopenia in endemic areas.en_US
dc.identifier.endpage85en_US
dc.identifier.issn1307-1068
dc.identifier.issn1308-5271
dc.identifier.issue2en_US
dc.identifier.startpage83en_US
dc.identifier.urihttps://hdl.handle.net/11616/102509
dc.identifier.volume3en_US
dc.identifier.wosWOS:000422189100008en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherAves Yayincilik, Ibrahim Karaen_US
dc.relation.ispartofJournal of Pediatric Infectionen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectIVIGen_US
dc.subjectBrucellaen_US
dc.subjectCorticosteroiden_US
dc.subjectThrombocytopeniaen_US
dc.titleBrusellaya Bagli Trombositopenik Purpuraen_US
dc.typeArticleen_US

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