Sporadic Creutzfeldt-Jakob Disease. First Clinical-Pathological Case Report in Ecuador.

被引:0
作者
Alarcon, Fernando [1 ]
Salinas, Roberto
Rabano, Alberto
机构
[1] Hosp Eugenio Espejo, Dept Neurol, Quito, Ecuador
来源
REVISTA ECUATORIANA DE NEUROLOGIA | 2009年 / 18卷 / 03期
关键词
Sporadic Creutzfeldt Jakob Disease; Heidenhain Variant; Clinical Pathological Findings; DIAGNOSIS; MRI; MARKER; FLUID;
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction Sporadic Creutzfeldt-Jakob disease (sCJD) has not yet been described in Ecuador Methods We present a 53-year-old patient who came to the Neurology Department of the Eugenio Espejo Hospital because of clinical symptoms and EEG and MRI tests that met the criteria for a diagnosis of CJD. which was later confirmed by neuropathological findings Results That patient was admitted to the hospital because of visual impairments and ataxia During his stay in the hospital, in addition to blindness, myoclonus and bilateral cortico-spinal signs. the patient's cognitive functions declined rapidly and progressively The clinical symptoms, the EEG and MRI were highly suggestive of CJD. The neuropathological findings confirmed this diagnosis Conclusion We report the first case in Ecuador, with neuropathological confirmation, of a patient diagnosed with the Heidenham variant of sCJD
引用
收藏
页码:71 / 75
页数:5
相关论文
共 20 条
  • [1] [Anonymous], 1998, WKLY EPIDEMIOL REC, V73, P361
  • [2] Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease
    Bahn, MM
    Parchi, P
    [J]. ARCHIVES OF NEUROLOGY, 1999, 56 (05) : 577 - 583
  • [3] Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant"
    Cooper, SA
    Murray, KL
    Heath, CA
    Will, RG
    Knight, RSG
    [J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 2005, 89 (10) : 1341 - 1342
  • [4] Accuracy of diffusion-weighted MR imaging in the diagnosis of sporadic Creutzfeldt-Jakob disease
    Demaerel, P
    Sciot, R
    Robberecht, W
    Dom, R
    Vandermeulen, D
    Maes, F
    Wilms, G
    [J]. JOURNAL OF NEUROLOGY, 2003, 250 (02) : 222 - 225
  • [5] MR imaging of Creutzfeldt-Jakob disease
    Finkenstaedt, M
    Szudra, A
    Zerr, I
    Poser, S
    Hise, JH
    Stoebner, JM
    Weber, T
    [J]. RADIOLOGY, 1996, 199 (03) : 793 - 798
  • [6] The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
    Hsich, G
    Kinney, K
    Gibbs, CJ
    Lee, KH
    Harrington, MG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (13) : 924 - 930
  • [7] Prion diseases
    Knight, RSG
    Will, RG
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2004, 75 : I36 - I42
  • [8] Sporadic Creutzfeldt-Jakob disease -: Magnetic resonance imaging and clinical findings
    Meissner, B
    Köhler, K
    Körtner, K
    Bartl, M
    Jastrow, U
    Mollenhauer, B
    Schröter, A
    Finkenstaedt, M
    Windl, O
    Poser, S
    Kretzschmar, HA
    Zerr, I
    [J]. NEUROLOGY, 2004, 63 (03) : 450 - 456
  • [9] The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance
    Nozaki, I.
    Hamaguchi, T.
    Noguchi-Shinohara, M.
    Ono, K.
    Shirasaki, H.
    Komai, K.
    Kitamoto, T.
    Yamada, M.
    [J]. NEUROLOGY, 2006, 67 (03) : 531 - 533
  • [10] First symptom in sporadic Creutzfeldt-Jakob disease
    Rabinovici, GD
    Wang, PN
    Levin, J
    Cook, L
    Pravdin, M
    Davis, J
    DeArmond, SJ
    Barbaro, NM
    Martindale, J
    Miller, BL
    Geschwind, MD
    [J]. NEUROLOGY, 2006, 66 (02) : 286 - 287