Brain stem MRI signal abnormalities in CADASIL

被引:65
作者
Chabriat, H
Mrissa, R
Levy, C
Vahedi, K
Taillia, H
Iba-Zizen, MT
Joutel, A
Tournier-Lasserve, E
Bousser, MG
机构
[1] Hop Lariboisiere, Serv Neurol, F-75475 Paris, France
[2] Hop St Antoine, Serv Radiol, F-75571 Paris, France
[3] Fac Med Necker, Hop 15 20, Serv Neuroradiol, Paris, France
[4] Fac Med Necker, INSERM, U25, Paris, France
关键词
brain stem; CADASIL; cerebral arteries; hypersignals; magnetic resonance imaging;
D O I
10.1161/01.STR.30.2.457
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background-We recently showed that the severity of MRI signal abnormalities increases with age in CADASIL, an arteriopathy due to mutations of notch 3 gene on chromosome 19. Previous results also suggest that the various hemispheric subcortical areas have a different vulnerability to ischemia in this disease. The distribution of the lesions at the brain stem level has not yet been reported. Case Descriptions-We reviewed the MRIs of 68 affected patients having signal abnormalities in the hemispheric white matter to assess the distribution and clinical consequences of brain stem signal abnormalities in CADASIL. We found hypersignals on T2-weighted images in the brain stem in 45% of the subjects. The pens was more frequently involved (100%) than the mesencephalon (69%) and the medulla (35%). Hyposignals on T1-weighted images, at the brain stem level, were observed only in two thirds of these subjects. The lack of signal abnormalities reaching the brain stem surface and the absence of cerebellar lesions were noteworthy. Conclusions-Brain stem signal abnormalities observed in CADASIL are found in regions irrigated only by perforating arteries. These results support parallel observations made for CADASIL-associated signal abnormalities in the cerebral hemispheres and emphasize the importance of the angioarchitecture of the cerebral vasculature to explain why a condition characterized by a systemic vessel wall pathology is manifested only as a brain disease.
引用
收藏
页码:457 / 459
页数:3
相关论文
共 19 条
  • [1] AUTOSOMAL DOMINANT LEUKOENCEPHALOPATHY AND SUBCORTICAL ISCHEMIC STROKE - A CLINICOPATHOLOGICAL STUDY
    BAUDRIMONT, M
    DUBAS, F
    JOUTEL, A
    TOURNIERLASSERVE, E
    BOUSSER, MG
    [J]. STROKE, 1993, 24 (01) : 122 - 125
  • [2] Chabriat H., 1996, Neurology, V46, pA212
  • [3] CHABRIAT H, 1995, STROKE, V26, P1729
  • [4] Patterns of MRI lesions in CADASIL
    Chabriat, H
    Levy, C
    Taillia, H
    Iba-Zizen, MT
    Vahedi, K
    Joutel, A
    Tournier-Lasserve, E
    Bousser, MG
    [J]. NEUROLOGY, 1998, 51 (02) : 452 - 457
  • [5] CLINICAL SPECTRUM OF CADASIL - A STUDY OF 7 FAMILIES
    CHABRIAT, H
    VAHEDI, K
    IBAZIZEN, MT
    JOUTEL, A
    NIBBIO, A
    NAGY, TG
    KREBS, MO
    JULIEN, J
    DUBOIS, B
    DUCROCQ, X
    LEVASSEUR, M
    HOMEYER, P
    MAS, JL
    LYONCAEN, O
    LASSERVE, ET
    BOUSSER, MG
    [J]. LANCET, 1995, 346 (8980): : 934 - 939
  • [6] Ducros A, 1996, AM J HUM GENET, V58, P171
  • [7] Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
    Joutel, A
    Corpechot, C
    Ducros, A
    Vahedi, K
    Chabriat, H
    Mouton, P
    Alamowitch, S
    Domenga, V
    Cecillion, M
    Marechal, E
    Maciazek, J
    Vayssiere, C
    Cruaud, C
    Cabanis, EA
    Ruchoux, MM
    Weissenbach, J
    Bach, JF
    Bousser, MG
    TournierLasserve, E
    [J]. NATURE, 1996, 383 (6602) : 707 - 710
  • [8] Asymptomatic pontine lesions found by magnetic resonance imaging: Are they central pontine myelinolysis?
    KleinschmidtDeMasters, BK
    Anderson, CA
    Rubinstein, D
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 149 (01) : 27 - 35
  • [9] NAKAI K, 1989, SCANNING MICROSCOPY, V3, P337
  • [10] PONTINE ISCHEMIC RAREFACTION
    PULLICINO, P
    OSTROW, P
    MILLER, L
    SNYDER, W
    MUNSCHAUER, F
    [J]. ANNALS OF NEUROLOGY, 1995, 37 (04) : 460 - 466