Multiparametric MRI Evaluation of Developmental Venous Anomalies in the Brain: Association with Signal Changes on FLAIR in Patients with Multiple Sclerosis

被引:2
|
作者
Sagtas, Ergin [1 ]
Guneyli, Serkan [2 ]
Akyilmaz, Dincer Aydin [3 ]
Yavas, Huseyin Gokhan [1 ]
Cakmak, Pinar [1 ]
Ufuk, Furkan [1 ]
机构
[1] Pamukkale Univ, Dept Radiol, Sch Med, Denizli, Turkey
[2] Koc Univ, Dept Radiol, Sch Med, Davutpasa Cad,4 Topkapi, TR-34010 Istanbul, Turkey
[3] Gaziantep Hatem Hosp, Dept Radiol, Gaziantep, Turkey
关键词
Developmental venous anomaly; fluid-attenuated inversion recovery; magnetic resonance imaging; multiple sclerosis; susceptibility-weighted imaging; FLAIR; CENTRAL VEIN SIGN; INTENSITY ABNORMALITIES; COLLAGENOSIS; PERFUSION; LESIONS; PREVALENCE; VENOGRAPHY; DIAGNOSIS; CHILDREN; ANGIOMA;
D O I
10.2174/1573405616666200516172759
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Developmental venous anomalies (DVAs) can be determined on magnetic resonance imaging (MRI), and they may be associated with multiple sclerosis (MS) lesions. Purpose: The objective was to evaluate the MRI findings of DVAs in the brain, to compare the prevalence of them between MS patients and control subjects, and to investigate the correlation of DVA-associated fluid-attenuated inversion recovery (FLAIR) hyperintensities and MRI-derived parameters between MS patients and control subjects having DVA. Methods: Total 160 patients with a mean age of 45 +/- 16 years who underwent multiparametric MRI including susceptibility-weighted imaging (SWI), diffusion-weighted imaging, 3D FLAIR, and contrast-enhanced imaging were included in this retrospective study. First, the presence of DVA was compared between the MS and control groups using the Chi-square test. Then, among the subjects having DVA, age, gender, and MRI-derived parameters such as the signal increase of DVA on FLAIR, location, and drainage of DVA were compared between the MS and control groups using Chi-square test. Results: The presence of DVA did not differ between the MS and control groups (P = 0.828). Signal increase around DVA on FLAIR (P = 0.03) and the age of less than 45 years demonstrated a significant correlation with MS group (P = 0.022). Conclusion: In our study, DVAs were effectively detected using SWI and 3D contrast-enhanced T-1-weighted imaging on MRI. The signal increase of DVA was better revealed on 3D FLAIR on MRI, and it was the only significant MRI-derived parameter in patients with MS.
引用
收藏
页码:928 / 935
页数:8
相关论文
共 50 条
  • [41] Sex-related differences in upper limb motor function in healthy subjects and multiple sclerosis patients: a multiparametric MRI study
    Bonacchi, Raffaello
    Valsasina, Paola
    Pagani, Elisabetta
    Meani, Alessandro
    Preziosa, Paolo
    Rocca, Maria A.
    Filippi, Massimo
    JOURNAL OF NEUROLOGY, 2023, 270 (11) : 5235 - 5250
  • [42] Sex-related differences in upper limb motor function in healthy subjects and multiple sclerosis patients: a multiparametric MRI study
    Raffaello Bonacchi
    Paola Valsasina
    Elisabetta Pagani
    Alessandro Meani
    Paolo Preziosa
    Maria A. Rocca
    Massimo Filippi
    Journal of Neurology, 2023, 270 : 5235 - 5250
  • [43] Contribution of cervical cord MRI and brain magnetization transfer imaging to the assessment of individual patients with multiple sclerosis:: a preliminary study
    Rovaris, M
    Holtmannspötter, M
    Rocca, MA
    Iannucci, G
    Codella, M
    Viti, B
    Campi, A
    Comi, G
    Yousry, TA
    Filippi, M
    MULTIPLE SCLEROSIS JOURNAL, 2002, 8 (01) : 52 - 58
  • [44] Structural and metabolic changes in the brain of patients with upper motor neuron disorders: A multiparametric MRI study
    Charil, Arnaud
    Corbo, Massimo
    Filippi, Massimo
    Kesavadas, Chandrasekharan
    Agosta, Federica
    Munerati, Elisabetta
    Gambini, Anna
    Comi, Giancarlo
    Scotti, Giuseppe
    Falini, Andrea
    AMYOTROPHIC LATERAL SCLEROSIS, 2009, 10 (5-6): : 269 - 279
  • [45] Using multiple imputation to efficiently correct cerebral MRI whole brain lesion and atrophy data in patients with multiple sclerosis
    Chua, Alicia S.
    Egorova, Svetlana
    Anderson, Mark C.
    Polgar-Turcsanyi, Mariann
    Chitnis, Tanuja
    Weiner, Howard L.
    Guttmann, Charles R. G.
    Bakshi, Rohit
    Healy, Brian C.
    NEUROIMAGE, 2015, 119 : 81 - 88
  • [46] Brain MRI lesions and atrophy are associated with employment status in patients with multiple sclerosis
    Shahamat Tauhid
    Renxin Chu
    Rahul Sasane
    Bonnie I. Glanz
    Mohit Neema
    Jennifer R. Miller
    Gloria Kim
    James E. Signorovitch
    Brian C. Healy
    Tanuja Chitnis
    Howard L. Weiner
    Rohit Bakshi
    Journal of Neurology, 2015, 262 : 2425 - 2432
  • [47] Brain MRI lesions and atrophy are associated with employment status in patients with multiple sclerosis
    Tauhid, Shahamat
    Chu, Renxin
    Sasane, Rahul
    Glanz, Bonnie I.
    Neema, Mohit
    Miller, Jennifer R.
    Kim, Gloria
    Signorovitch, James E.
    Healy, Brian C.
    Chitnis, Tanuja
    Weiner, Howard L.
    Bakshi, Rohit
    JOURNAL OF NEUROLOGY, 2015, 262 (11) : 2425 - 2432
  • [48] Correlation between brain MRI lesion volume and disability in patients with multiple sclerosis
    Mammi, S
    Filippi, M
    Martinelli, V
    Campi, A
    Colombo, B
    Scotti, G
    Canal, N
    Comi, G
    ACTA NEUROLOGICA SCANDINAVICA, 1996, 94 (02): : 93 - 96
  • [49] Brain Hemodynamic Changes Associated with Chronic Cerebrospinal Venous Insufficiency Are Not Specific to Multiple Sclerosis and Do Not Increase Its Severity
    Garaci, Francesco G.
    Marziali, Simone
    Meschini, Alessandro
    Fornari, Maria
    Rossi, Silvia
    Melis, Milena
    Fabiano, Sebastiano
    Stefanini, Matteo
    Simonetti, Giovanni
    Centonze, Diego
    Floris, Roberto
    RADIOLOGY, 2012, 265 (01) : 233 - 239
  • [50] Olfactory Evoked Potentials and Brain MRI Outcomes in Multiple Sclerosis Patients: A Cross-Sectional Study
    Ciurleo, Rosella
    De Salvo, Simona
    Caminiti, Fabrizia
    Militi, Annalisa
    Bonanno, Lilla
    JOURNAL OF CLINICAL MEDICINE, 2025, 14 (01)