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Japanese

Polyuria and Polydipsia in a Young Boy:A Case Study Kazuo KINOSHITA 1 , Yuzo YAMAKAWA 1 , Tadanobu KURIBAYAAHI 2 , Motohisa NAGAMINE 2 1Department of Neurosurgery, Miyazaki Medical College 2The Third Department of Internal Medicine, Miyazaki Medical College Keyword: Intracranial teratoma , Germinoma , Melanotic progonoma , Panhypopituitarism pp.1035-1043
Published Date 1979/11/10
DOI https://doi.org/10.11477/mf.1436201063
  • Abstract
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A 13-year-old boy with a teratoma in the sellar region was presented.

This patient had gradually developed polyuria and polydipsia since 2 years prior to the first admission. Endocrinological examination showed a marked reduction of pituitary function. Careful neuroradiological examinations including CT failed to show any mass lesion in the sellar and suprasellar regions but a marked increase of the width of the third ventricle. CSF examination revealed only a slight increase of cell count (lymphocytes).The patient was discharged with hormonal replacement therapy.


Copyright © 1979, 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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