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Published Online: May 2000

Relationship Between MRI Findings and Prognosis for Patients With General Paresis

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences

Abstract

MRI was performed in 7 patients with general paresis before or at a very early stage of treatment. A large dose of antibiotics, mainly penicillin, was given to all patients, and the effects of treatment, the patients' outcome, and MRI findings were investigated. Three of the 7 patients had MRI findings of atrophy of the medial temporal lobe including the hippocampus. In the medial temporal lobe atrophy group, a personality change or general dementia remained even after the treatment was completed, and outcome in social functioning was poor. Medial temporal lobe atrophy may be a poor prognostic sign in general paresis.

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Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: 246 - 250
PubMed: 11001604

History

Published in print: May 2000
Published online: 24 January 2015

Authors

Affiliations

Kazuhiro Kodama, M.D., Ph.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]
Shin-ichi Okada, M.D., Ph.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]
Naoya Komatsu, M.D., Ph.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]
Naoto Yamanouchi, M.D., Ph.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]
Shingo Noda, M.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]
Chikara Kumakiri, M.D., Ph.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]
Toshio Sato, M.D., Ph.D.
Received September 3, 1998; revised August 2, 1999; accepted October 7, 1999. From the Department of Neuropsychiatry, Chiba University School of Medicine, Chiba, Japan. Address correspondence to Dr. Kodama, Department of Neuropsychiatry, Chiba University School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan; e-mail: [email protected]

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