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dc.contributor.authorDevecioglu, Omer
dc.contributor.authorDemir, Muzaffer
dc.contributor.authorBiner, Betul
dc.date.accessioned2021-03-05T17:06:38Z
dc.date.available2021-03-05T17:06:38Z
dc.date.issued2007
dc.identifier.citationBiner B., Devecioglu O., Demir M., "Pitfalls in the diagnosis of immune thrombocytopenic purpura in children: 4 case reports", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, cilt.13, ss.329-333, 2007
dc.identifier.issn1076-0296
dc.identifier.othervv_1032021
dc.identifier.otherav_c3ec2a54-1d93-4f48-9b5a-c85032fe7e58
dc.identifier.urihttp://hdl.handle.net/20.500.12627/129976
dc.identifier.urihttps://doi.org/10.1177/1076029607302444
dc.description.abstractAcute idiopathic thrombocytopenic purpura is the most common cause of thrombocytopenia in childhood, and diagnosis of idiopathic thrombocytopenic purpura is made clinically based on the exclusion of other causes of thrombocytopenia. Patients with diverse causes of thrombocytopenia are sometimes erroneously diagnosed as having idiopathic thrombocytopenic purpura. However, for the prevention of misdiagnoses, careful inspection of peripheral blood smear is of utmost importance. This report presents 4 cases presumed as acute idiopathic thrombocytopenic purpura that were finally identified as pseudothrombocytopenia, inherited macrothrombocytopenia (MHY9 disorders) possibly Epstein syndrome, Bernard-Soulier syndrome, and drug-induced thrombocytopenia. They draw attention to the importance of platelet morphology to exclude inherited macrodirombocytopenia and history to exclude drug-induced thrombocytopenia. Better diagnostic approaches would be possible by the awareness of these relatively rare causes of isolated thrombocytopenia.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectHematoloji
dc.subjectHEMATOLOJİ
dc.subjectİç Hastalıkları
dc.subjectKlinik Tıp (MED)
dc.subjectPERİFERAL VASKÜLER HASTALIĞI
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titlePitfalls in the diagnosis of immune thrombocytopenic purpura in children: 4 case reports
dc.typeMakale
dc.relation.journalCLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
dc.contributor.department, ,
dc.identifier.volume13
dc.identifier.issue3
dc.identifier.startpage329
dc.identifier.endpage333
dc.contributor.firstauthorID183318


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