{"created":"2023-05-15T12:16:42.025892+00:00","id":348,"links":{},"metadata":{"_buckets":{"deposit":"23756de9-32e4-4c3a-8d9b-f5d37cf627a6"},"_deposit":{"created_by":4,"id":"348","owners":[4],"pid":{"revision_id":0,"type":"depid","value":"348"},"status":"published"},"_oai":{"id":"oai:aino.repo.nii.ac.jp:00000348","sets":["7:39"]},"author_link":["1136","1137"],"item_3_biblio_info_12":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2009-03-31","bibliographicIssueDateType":"Issued"},"bibliographicVolumeNumber":"7","bibliographic_titles":[{},{"bibliographic_title":"Aino journal","bibliographic_titleLang":"en"}]}]},"item_3_description_11":{"attribute_name":"抄録(英)","attribute_value_mlt":[{"subitem_description":"A 76y male suffering from progressive dementia (Hasegawa's dementia scale = 6), urinary incontinence, and gate disturbance received CSF shunting. The clinical findings of MRI, CT-cisternography, and a CSF-tap test were not typical for idiopathic normal pressure hydrocephalus (iNPH); rather, the MRI showed brain atrophy. The decision to perform shunting surgery was made due to the clinical manifestation of progressive dementia, and fortunately, it was successful. Senile brain atrophy does not rule out hydrocephalus. The indication of CSF shunting for senile iNPH is outlined. 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