Nicolai A, Lazzarino L G, Alari E
Divisione Neurologica, Ospedale Civile, Gorizia, Italy.
Clin Neuropathol. 1991 Jan-Feb;10(1):16-20.
The authors describe the case of a patient showing clinical symptoms consistent with a partial Klüver-Bucy syndrome. CT-scan, macroscopic and histological findings showed the presence of a multicentric glioblastoma with almost exclusive involvement of subcortical gray nuclei and white matter. The possible anatomo-clinical correlations of these unusual locations in KBS are discussed. In addition, the authors emphasize that KBS can arise not only from lesions located in the temporal cortex and/or amygdala, but also from strategically located subcortical lesions particularly involving striatal nuclei and subcortical white matter in the insular area.
作者描述了一例表现出与部分克吕弗-布西综合征相符的临床症状的患者病例。CT扫描、大体及组织学检查结果显示存在多中心性胶质母细胞瘤，几乎仅累及皮质下灰质核团和白质。文中讨论了这些在克吕弗-布西综合征中不寻常部位可能的解剖学与临床关联。此外，作者强调克吕弗-布西综合征不仅可由位于颞叶皮质和/或杏仁核的病变引起，还可由位于关键部位的皮质下病变引起，特别是累及岛叶区域的纹状体核团和皮质下白质的病变。
