[伴有罕见病变部位（所谓的海登海因综合征）的克雅氏病病例]
[Case of Jakob-Creutzfeldt disease with rarely observed location of lesions (the so-called Heidenhain syndrome)].
作者信息
Iwanowski L, Kunicka J
出版信息
Neurol Neurochir Pol. 1977 Mar-Apr;11(2):247-50.
PMID:323741
Abstract
The authors describe a case of Jakob-Creutzfeldt disease in a 64-year-old women. The peculiarity of the case lay in the fact that besides atrophic lesions of frontal lobes, extensive spongiform degeneration was present in both occipital lobes--corresponding to the so-called Heidenhain syndrome of classical neuropathology. The clinical counterpart of this location of the lesions, apart from dementia, were quadrantic hemianopsia and changes in EEG records.
摘要
作者描述了一例64岁女性患雅各布-克雅氏病的病例。该病例的特殊之处在于，除额叶萎缩性病变外，双侧枕叶均出现广泛的海绵状变性，这与经典神经病理学中所谓的海登海因综合征相对应。除痴呆外，这些病变部位在临床上对应的表现为象限性偏盲和脑电图记录的变化。
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