Publication:
Evaluation of parenchymal neuro-Behcet disease by using susceptibility-weighted imaging

dc.contributor.coauthorAlbayram, S.
dc.contributor.coauthorSaip, S.
dc.contributor.coauthorHasiloglu, Z. I.
dc.contributor.coauthorTeke, M.
dc.contributor.coauthorTutuncu, M.
dc.contributor.coauthorSelcuk, H.
dc.contributor.coauthorKina, A.
dc.contributor.coauthorSiva, A.
dc.contributor.kuauthorCeyhan, Elvan
dc.date.accessioned2024-11-09T23:10:16Z
dc.date.issued2011
dc.description.abstractBACKGROUND and PURPOSE: Neurologic involvement in Behcet disease, also known as NBD, is one of the most devastating manifestations of the disease. The precise pathologic mechanism of parenchymal NBD lesions has not been established. We evaluated lesion characteristics and probable venous hemorrhage in parenchymal NBD by using SWI, and we compared the imaging results with conventional MR imaging sequences. MATERIALS and METHODS: We performed cranial MR imaging by using a 1.5T scanner in 23 patients with a definitive diagnosis of parenchymal NBD. We compared the proportion of lesion detection and the performance of hemorrhagic detection with the T2 FSE, T2*GE, and SWI magnitude, and SWI mIP by using the chi(2) test. RESULTS: The proportion of lesion detection with both SWI magnitude and SWI MinMIP was significantly larger than that with T2*GE. The proportions of lesion detection among all other pairs of methods were not significantly different according to the corresponding P value (chi(2) = 17.4929, df = 3, P = .0006). Proportions of hypointense hemorrhagic lesions with 12 FSE and T2*GE were not significantly different, and likewise for the proportions of hypointense hemorrhagic lesions with SWI magnitude and SWI mIP. In contrast, the proportions of hypointense hemorrhagic lesions with SWI magnitude and SWI mIP were significantly larger than that with 12 FSE and T2*GE (chi(2) = 108.5396, df = 3, P < .0001). CONCLUSIONS: Most of the lesions in parenchymal NBD were found to be hemorrhagic with SWI, supporting the proposed venous theory in pathology. In addition, compared with T2 FSE and T2*GE sequences, SWI was more successful in the determination of widespread involvement of the disease, particularly in nonchronic cases.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.issue6
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume32
dc.identifier.doi10.3174/ajnr.A2477
dc.identifier.eissn1936-959X
dc.identifier.issn0195-6108
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-79959315334
dc.identifier.urihttps://doi.org/10.3174/ajnr.A2477
dc.identifier.urihttps://hdl.handle.net/20.500.14288/9445
dc.identifier.wos292066600016
dc.keywordsDiffuse Axonal Injury
dc.keywordsNervous-System
dc.keywordsNeurological Involvement
dc.keywordsMr Venography
dc.keywordsLesions
dc.keywordsContrast
dc.keywordsChildren
dc.language.isoeng
dc.publisherAmer Soc Neuroradiology
dc.relation.ispartofAmerican Journal of Neuroradiology
dc.subjectClinical neurology
dc.subjectNeuroimaging
dc.subjectRadiology, Nuclear medicine
dc.subjectMedical imaging
dc.titleEvaluation of parenchymal neuro-Behcet disease by using susceptibility-weighted imaging
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorCeyhan, Elvan

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