Trombocytopenia related to colchicine: Report of two cases

dc.contributor.authorKarakurt, Neslihan
dc.contributor.authorCandir, Mehmet Onur
dc.contributor.authorKosan Culha, Vildan
dc.contributor.authorYarali, Nese
dc.contributor.authorCakar, Nilgun
dc.contributor.authorOzbek, Namik
dc.date.accessioned2022-02-16T13:08:21Z
dc.date.available2022-02-16T13:08:21Z
dc.date.issued2017
dc.departmentİnönü Üniversitesien_US
dc.description.abstractFamilial Mediterranean fever (FMF) is the most frequent autoinflammatory disease which can be well controlled with lifelong use of colchicine. Daily colchicine use has been shown to reduce the frequency, severity, and duration of attacks. Colchicine also has been found to be effective in decreasing the prevalence of amyloidosis. Therapeutic oral dose of colchicine (0.5-2.0 mg/ day) may cause cramping, abdominal pain, hyperperistalsis, diarrhea and vomiting. Besides, colchicine may rarely cause bone marrow failure, agranulocytosis and/ or thrombocytopenia as well. Here in we report two pediatric cases of FMF who developed trombocytopenia after colchicine medication and call attention to colchicine related trombocytopenia.en_US
dc.identifier.citationKarakurt, N., Onur Candir, M., Kosan Culha, V., Yarali, N., Cakar, N., & Ozbek, N. (2021). Trombocytopenia related to colchicine: Report of two cases . Annals of Medical Researchen_US
dc.identifier.doi10.5455/jtomc.2016.09.103en_US
dc.identifier.urihttps://hdl.handle.net/11616/47314
dc.language.isoenen_US
dc.relation.ispartofAnnals of Medical Researchen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleTrombocytopenia related to colchicine: Report of two casesen_US
dc.typeArticleen_US

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