Updated on 2025/03/27

写真a

 
Tauchi Hisamichi
 
Organization
Graduate School of Medicine Program for Medical Sciences Professor
Title
Professor
Contact information
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Degree

  • 医学博士 ( 2008.10   愛媛大学 )

Research Interests

  • Hematology

  • Pediatrics

  • 血液内科学

  • 小児科学

Research Areas

  • Life Science / Embryonic medicine and pediatrics

  • Life Science / Hematology and medical oncology

Education

  • Ehime University   Faculty of Medicine

    - 1989

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  • Ehime University   School of Medicine   Faculty of Medicine

    - 1989

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    Country： Japan

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Professional Memberships

MISC

  • Clinical investigation of childhood tuberculosis and chemoprophylaxis

    17 ( 4 )   393   1998

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  • Clinical investigation of childhood tuberculosis and chemoprophylaxis

    17 ( 4 )   393   1998

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  • 小児の結核と抗結核剤予防内服の臨床的検討

    愛媛医学   17 ( 4 )   393   1998

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  • A Case of Virus-Associated Hemophagocytic Syndrome, with Malignant Histiocytosis-like Bone Marrow Findings.

    田内 久道, 石田 也寸志, 井上 哲志, 横田 佳子, 松田 博

    日本小児血液学会雑誌   7 ( 3 )   274 - 277   1993

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  • A Case of Virus-Associated Hemophagocytic Syndrome, with Malignant Histiocytosis-like Bone Marrow Findings.

    Hisamichi TAUCHI, Yasushi ISHIDA, Tetsushi INOUE, Yoshiko YOKOTA, Hiroshi MATSUDA

    The Japanese Journal of Pediatric Hematology   7 ( 3 )   274 - 277   1993

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  • 骨髄細胞診ではmalignant histiocytosis様の所見を示したVAHSの1例

    田内 久道, 石田 也寸志, 井上 哲志, 横田 佳子, 松田 博

    日本小児血液学会雑誌   7 ( 3 )   274 - 277   1993

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  • The First Case of Infantile Type Neuronal Ceroid-Lipofuscinosis in Japan

    Hisamichi Tauchi, Nozomi Sano, Takehiko Morimoto, Hideo Nagao, Hiroshi Matsuda

    No To Hattatsu   24 ( 6 )   595 - 599   1992

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    Language：English  

    We reported the first case of typical infantile-type neuronal ceroid-lipofuscinosis (INCL) in Japan. The patient was a 1-year-old girl presenting with rapidly progressive psychomotor deterioration and blindness. Muscular hypotonia, microcephaly and myoclonic jerks became marked with the progression of her disease. Diminution in amplitude of EEG, VEP and ERG was prominent in the initial stage, but ABR was normal. MRI showed progressive brain atrophy. Electron microscopic examination of the biopsied skin revealed granular matrix, the specific inclusion bodies, in the epithelial cell of sweet glands. Many sea-blue histiocytes were demonstrated in her bone marrow samples. INCL is a common progressive encephalopathy in the Scandinavian countries, but a typical case had not yet been fully reported in Japan. This prompted us to report our case. Future reports are need for the study of INCL in Japan. © 1992, The Japanese Society of Child Neurology. All rights reserved.

    DOI： 10.11251/ojjscn1969.24.595

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  • The First Case of Infantile Type Neuronal Ceroid-Lipofuscinosis in Japan

    Hisamichi Tauchi, Nozomi Sano, Takehiko Morimoto, Hideo Nagao, Hiroshi Matsuda

    No To Hattatsu   24 ( 6 )   595 - 599   1992

    　More details

    Language：English  

    We reported the first case of typical infantile-type neuronal ceroid-lipofuscinosis (INCL) in Japan. The patient was a 1-year-old girl presenting with rapidly progressive psychomotor deterioration and blindness. Muscular hypotonia, microcephaly and myoclonic jerks became marked with the progression of her disease. Diminution in amplitude of EEG, VEP and ERG was prominent in the initial stage, but ABR was normal. MRI showed progressive brain atrophy. Electron microscopic examination of the biopsied skin revealed granular matrix, the specific inclusion bodies, in the epithelial cell of sweet glands. Many sea-blue histiocytes were demonstrated in her bone marrow samples. INCL is a common progressive encephalopathy in the Scandinavian countries, but a typical case had not yet been fully reported in Japan. This prompted us to report our case. Future reports are need for the study of INCL in Japan. © 1992, The Japanese Society of Child Neurology. All rights reserved.

    DOI： 10.11251/ojjscn1969.24.595

    Scopus

    PubMed

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Research Projects

  • Study of stem cell Transplantation

    2000

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    Grant type：Competitive

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  • 幹細胞移植に関する研究

    2000

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    Grant type：Competitive

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