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A Case of Male Acromegaly with Galactorrhea Takayuki TOKUNAGA 1,2 , Takashi HAYASHI 1 , Eiichiro HONDA 1 , Naomi KIKUCHI 2 , Hidetsuna UTSUNOMIYA 3 1Department of Neurosurgery, St. Mary's Hospital 2Department of Neurosurgery, Kurume University School of Medicine 3Department of Neuroradiology, St. Mary's Hospital Keyword: Pituitary adenoma , Acromegaly , Prolactin growth hormone , Galactorrhea pp.1101-1105
Published Date 1988/8/10
DOI https://doi.org/10.11477/mf.1436202688
  • Abstract
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A 43-year-old man was admitted to our clinic with complaints of headache and nasal obstruction. He has noted increasing hand and foot size with decreasing libido and pollakiuria for ten years.

On admission, he showed galactorrhea. His visualsymptoms were slightly decreased. Endocrinological evaluation revealed high serum levels of GH and pro-lactin. A plain skull X-ray showed acromegalic features with remarkable destruction of dorsum sellae. A con-trast enhanced CT demonstrated an intrasellar high den-sity mass extending to the sphenoid sinus and the right ethmoidal sinus. A cerebral angiogram was normal.


Copyright © 1988, 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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