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dc.contributor.authorUludag, Murat
dc.contributor.authorOrnek, Nurettin Irem
dc.contributor.authorSari, Hidayet
dc.contributor.authorGulsen, Fatih
dc.contributor.authorAkarirmak, Ulku
dc.contributor.authorGun, Kerem
dc.date.accessioned2021-03-03T12:25:11Z
dc.date.available2021-03-03T12:25:11Z
dc.date.issued2014
dc.identifier.citationSari H., Uludag M., Akarirmak U., Ornek N. I. , Gun K., Gulsen F., "Aggressive vertebral hemangioma as a rare cause of myelopathy", JOURNAL OF BACK AND MUSCULOSKELETAL REHABILITATION, cilt.27, sa.2, ss.125-129, 2014
dc.identifier.issn1053-8127
dc.identifier.othervv_1032021
dc.identifier.otherav_2de6cdbc-4438-4cda-a813-8b93a0a75067
dc.identifier.urihttp://hdl.handle.net/20.500.12627/35438
dc.identifier.urihttps://doi.org/10.3233/bmr-130425
dc.description.abstractVertebral hemangiomas (VHs) are common lesions in the adult population. They are usually asymptomatic and found incidentally on radiological imaging. New-onset back pain followed by subacute progression of thoracal myelopathy is the most common presentation in patients with neurological deficit. Differential diagnoses would include metastasis, multiple myeloma, lymphoma, Paget disease, osseous tumors such as Ewing sarcoma or hemangioblastoma and blood dyscrasia. We present a 41 year-old-male patient with thoracal VH causing myelopathy that completely improved after rehabilitation program with embolization and vertebroplasty procedures.
dc.language.isoeng
dc.subjectREHABİLİTASYON
dc.subjectCerrahi Tıp Bilimleri
dc.subjectORTOPEDİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectOrtopedi ve Travmatoloji
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectFiziksel Tıp ve Rehabilitasyon
dc.titleAggressive vertebral hemangioma as a rare cause of myelopathy
dc.typeMakale
dc.relation.journalJOURNAL OF BACK AND MUSCULOSKELETAL REHABILITATION
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume27
dc.identifier.issue2
dc.identifier.startpage125
dc.identifier.endpage129
dc.contributor.firstauthorID76778


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