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dc.contributor.authorDIZ-KUCUKKAYA, Reyhan
dc.contributor.authorArtim-Esen, Bahar
dc.contributor.authorInanc, Murat
dc.date.accessioned2021-03-06T08:14:37Z
dc.date.available2021-03-06T08:14:37Z
dc.date.issued2015
dc.identifier.citationArtim-Esen B., DIZ-KUCUKKAYA R., Inanc M., "The Significance and Management of Thrombocytopenia in Antiphospholipid Syndrome", CURRENT RHEUMATOLOGY REPORTS, cilt.17, 2015
dc.identifier.issn1523-3774
dc.identifier.otherav_dfefcc12-2f85-4766-9824-bbee7ace8b27
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/147514
dc.identifier.urihttps://doi.org/10.1007/s11926-014-0494-8
dc.description.abstractThe association between antiphospholipid antibodies (aPL) and clinical problems goes beyond what is stated in the antiphospholipid syndrome (APS) classification criteria, namely thrombosis and pregnancy morbidity, and thrombocytopenia is the most common non-criteria hematologic manifestation of aPL with a frequency ranging from 20 to 50 %. Thrombocytopenia is rarely severe, and hemorrhage is far less common than thrombosis. However, when anticoagulation is considered, it may constitute a clinical problem with increased bleeding risk. Furthermore, thrombocytopenia represents a risk factor for thrombosis in aPL-positive patients. Therefore, it is important to understand the pathogenesis and the clinical associations of thrombocytopenia to build the right medical approach in aPL-positive patients. In this paper, we review the literature on aPL/APS-associated thrombocytopenia and briefly discuss the other conditions that can result in thrombocytopenia as they have commonalities with APS and their recognition is important to establish the most appropriate treatment strategy.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectİmmünoloji ve Romatoloji
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleThe Significance and Management of Thrombocytopenia in Antiphospholipid Syndrome
dc.typeMakale
dc.relation.journalCURRENT RHEUMATOLOGY REPORTS
dc.contributor.departmentGrup Florence Nigtingale Hospital Turkey , ,
dc.identifier.volume17
dc.identifier.issue3
dc.contributor.firstauthorID71817


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