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dc.contributor.authorEtli, Mustafa
dc.contributor.authorKarahan, Oğuz
dc.date.accessioned2023-11-30T06:54:44Z
dc.date.available2023-11-30T06:54:44Z
dc.date.issued2021en_US
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-85109865177&origin=resultslist&sort=plf-f&src=s&nlo=&nlr=&nls=&sid=20c4fe371b9b908d4f7e419f791331ff&sot=aff&sdt=cl&cluster=scofreetoread%2c%22all%22%2ct&sl=72&s=AF-ID%28%22Alanya+Alaaddin+Keykubat+University%22+60198720%29+AND+SUBJAREA%28MEDI%29&relpos=132&citeCnt=0&searchTerm=
dc.identifier.urihttps://hdl.handle.net/20.500.12868/2445
dc.identifier.urihttps://www.scielo.br/j/jvb/a/CLd56y8hpp7kDP6Ngjxttxj/?lang=en
dc.identifier.urihttps://www.scielo.br/j/jvb/a/CLd56y8hpp7kDP6Ngjxttxj/?lang=en
dc.description.abstractMoyamoya disease is a rare disorder that involves the cerebrovascular system. Usually, it leads to occlusion of the arteries of the cerebral system and causes cerebral circulatory complaints. A 48-year-old female patient was admitted to our clinic with intermittent claudication in both legs. Biphasic and monophasic waveform patterns were detected bilaterally in distal (trifurcation arteries) lower extremities with Doppler sonography. The patient therefore underwent systemic vascular examination. Computed tomography angiography revealed bilateral carotid occlusion at the level of supraclinoid segments, and opacifications were detected at the distal segments of the bilateral anterior cerebellar and middle cerebellar arteries. The patient was diagnosed with moyamoya disease, and anticoagulant treatment was started. In conclusion, most previous reports have presented the cerebrovascular involvement of moyamoya disease. However, this disease can involve different peripheral vascular systems and careful and systemic vascular examination is necessary for an exact diagnosis.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1590/1677-5449.200216en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMoyamoya diseaseen_US
dc.subjectCerebrovascular diseaseen_US
dc.subjectPopliteal arteryen_US
dc.subjectUnusual involvementen_US
dc.titleUnusual presentation of moyamoya disease with popliteal involvement: Case report and review of the literatureen_US
dc.typearticleen_US
dc.contributor.departmentALKÜ, Fakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.identifier.volume20en_US
dc.relation.journalJornal Vascular Brasileiroen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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