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Solitary Actinomycotic Brain Abscess: Case Report Kiyoshi Takahashi 1 , Yoshihito Hasegawa 1 , Yo Nishimoto 1 , Satoru Hayashi 1 , Masahiro Yamasaki 2 , Daisuke Kuzume 2 , Keiko Hashimoto 2 , Hideaki Enzan 3 1Department of Neurosurgery,Chikamori Hospital 2Department of Neurology,Chikamori Hospital 3Department of Pathology,Chikamori Hospital Keyword: Actinomyces , Nocardia , brain abscess , thallium , infection pp.689-695
Published Date 2012/6/1
DOI https://doi.org/10.11477/mf.1416101222

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Abstract

 Actinomycotic brain abscess is a rare condition with uncertain clinical features. Here we report the case of a 66-year-old immune-competent woman with an actinomycotic brain abscess who presented with sensory aphasia and mild right hemiparesis. She had no febrile episode or headache. Moreover, she did not have any periodontal or oto-rhino-laryngological disease, and the results of laboratory tests were normal. A computed tomography scan showed an irregular, low-density area in the left parietal lobe. Subsequent magnetic resonance imaging showed low-signal intensity in a T1 weighted image, high-signal intensity in a T2 weighted image, and mixed intensity on a diffusion weighted image. Thallium-201 chloride scintigraphy showed definite accumulation of thallium in the lesion and the patient's condition gradually deteriorated. Ten days after gadolinium administration, a T1 weighted image showed a multi- lobulated irregular mass in the left parietal lobe. The patient subsequently underwent craniotomy and evacuation of the yellowish abscess. Gram staining of the tissue showed the presence of gram-positive filamentous rods, and abscess cultures were positive for Actinomyces and Prevotella disiens. The abscess resolved after treatment with a high dose of intravenous penicillin G (24 million units/day) for 8 weeks, followed by an oral dose of amoxicillin for 4 months. The patient was discharged with a rudimentary limitation of the visual field.

(Received: October 20,2011,Accepted: December 28,2011)


Copyright © 2012, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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