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dc.contributor.authorKayatas, Kadir
dc.contributor.authorKARATOPRAK, CUMALİ
dc.contributor.authorBenzer, Muhammet
dc.contributor.authorDemirtunc, Refik
dc.contributor.authorDemirkesen, Cuyan
dc.contributor.authorCebeci, Filiz
dc.date.accessioned2021-03-04T11:12:45Z
dc.date.available2021-03-04T11:12:45Z
dc.date.issued2013
dc.identifier.citationKayatas K., Cebeci F., KARATOPRAK C., Benzer M., Demirtunc R., Demirkesen C., "Factor V Leiden Mutation-Related Chronic Skin Ulcers", INTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS, cilt.12, sa.1, ss.35-38, 2013
dc.identifier.issn1534-7346
dc.identifier.othervv_1032021
dc.identifier.otherav_71265936-e14c-4d04-988d-e41d9d57bb97
dc.identifier.urihttp://hdl.handle.net/20.500.12627/77963
dc.identifier.urihttps://doi.org/10.1177/1534734613479379
dc.description.abstractChronic skin ulcers require extensive, systemic differential diagnosis; thus, they are difficult to diagnose and treat. Transient or persistent hypercoagulable states are among the rare causes of skin ulcers. Here, we present the case of a 27-year-old woman patient with recurrent, nonhealing skin ulcers of 8 years' duration, who had been treated unsuccessfully with various medications under different diagnoses at different clinics. On admission, a skin biopsy demonstrated occlusive vasculopathy, and the search for an inherited hypercoagulable state revealed a heterozygous factor V Leiden mutation. The patient was treated with anticoagulants and hyperbaric oxygen. On treatment, the skin lesions healed and did not recur.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectDermatoloji
dc.subjectCerrahi Tıp Bilimleri
dc.subjectDERMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectCERRAHİ
dc.subjectTıp
dc.titleFactor V Leiden Mutation-Related Chronic Skin Ulcers
dc.typeMakale
dc.relation.journalINTERNATIONAL JOURNAL OF LOWER EXTREMITY WOUNDS
dc.contributor.departmentIstanbul Haydarpasa Numune Training & Research Hospital , ,
dc.identifier.volume12
dc.identifier.issue1
dc.identifier.startpage35
dc.identifier.endpage38
dc.contributor.firstauthorID208577


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