Multiple Neuroepithelial Tumors of Different Cell Types : Case Report
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概要
- 論文の詳細を見る
延髄および上位頚随に生じた多発性随内腫瘍の1例を報告した。症例は22歳男性、四肢麻痺にて発症。MRIでは延髄に低吸収域を認めた。腫瘍は全摘出され、その病理所見はpilocytic astrocytomaであった。9年後、右上肢の筋力低下と知覚異常を訴え、再び入院。MRIでは、上位頚随随内に腫瘍を認めた。腫瘍は摘出され、その病理所見はependymomaであった。このように多発性のneuroepithelial tumorで、かつ病理所見が異なる症例は、本例を含めて8例しか報告されていない。本症例では、隣接する部位に異なるneuroepithlial tumorが存在しており、primitive spongioblastが分化しつつ拡がる過程において腫瘍化し、astrocytomaとependymomaが生じたと推測された。
- 日本脳神経外科学会の論文
- 1995-12-15
著者
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Asahi Takashi
Department Of Neurosurgery Faculty Of Medicine University Of Toyama
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赤井 卓也
国立水戸病院脳神経外科
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Sonobe Makoto
国立水戸病院脳神経外科
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Asahi Takashi
Faculty Of Medicine Department Of Physiology Toyama Medical And Pharmaceutical University
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TAKAHASHI Shinichiro
国立水戸病院脳神経外科
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SUGITA Kyouichi
国立水戸病院脳神経外科
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赤井 卓也
Department of Neurosurgery, Faculty of Medicine, University of Toyama
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