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Japanese

A CASE OF BILATERAL POLYNODULAR ADRENOCORTICAL HYPERPLASIA Masaharu Takanami 1 , Masaharu Tajima 1 , Masahiro Matsushima 1 , Ko Ando 1 , Shigeji Baba 2 , Toshihiko Atobe 3 1Department of Urology, Toho University School of Medicine 24th Department of Internal Medicine, Toho University School of Medicine 3Research Laboratory of Pathology (Ohashi), Toho University School of Medicine pp.657-659
Published Date 1986/8/20
DOI https://doi.org/10.11477/mf.1413204326
  • Abstract
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We experienced a case of bilateral polynodular adrenocortical hyperplasia, which was the 22nd case to be reported in the Japanese literature. The patient was a 55-year-old Japanese female, with symptoms typical of Cushing's syndrome including moon face, obesity, poor muscle development and poor wound healing. She underwent bilateral total adrenalectomy for bilateral adrenocortical hyper-plasia which was diagnosed by specific hormonal tests for Cushing's syndrome and by CT scan.


Copyright © 1986, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1332 印刷版ISSN 0385-2393 医学書院

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