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Pituitary Adenoma Associated with Neurofibromatosis Type 1:Case Report Kazuhiko KUROZUMI 1,4 , Akira TABUCHI 1 , Yasuhiro ONO 1 , Takashi TAMIYA 1 , Takashi OHMOTO 1 , Tomohisa FURUTA 2 , Shuji HAMASAKI 3 1Department of Neurological Surgery, Field of Neuroscience, Branch of Biophysical Science, Graduate School of Medicine and Dentistry, Okayama University 2Department of Clinical Psychology, School of Social Welfare, Kibi International University 3Department of Pathology, Okayama University Hospital Keyword: phakomatosis , neurofibromatosis type1 , pituitary adenoma , clinically silent corticotroph pituitary adenoma pp.741-745
Published Date 2002/7/10
DOI https://doi.org/10.11477/mf.1436902239
  • Abstract
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A case of pituitary adenoma associated is neurofibromatosis type 1 is reported. On June 6,2000, a 49-year-old man was admitted to the Department of Neurological Surgery, Okayama University Hospital, for bitemporal hemianopsia. Twenty-nine years previously, he had been operated on for a left inguinal tumor that proved to be a neurofibroma. Based on the presence of other manifestations, such as cafe-au-lait spots and subcutaneous nodules, he had been di-agnosed with neurofibromatosis type 1, the same as his father, sister, and daughter.


Copyright © 2002, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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