Pathophysiology and treatment of subclinical Cushing’s disease and pituitary silent corticotroph adenomas [Review]

Author:

Kageyama Kazunori12,Oki Yutaka3,Nigawara Takeshi1,Suda Toshihiro4,Daimon Makoto1

Affiliation:

1. Department of Endocrinology and Metabolism, Hirosaki University Graduate School of Medicine, Hirosaki 036-8562, Japan

2. Department of Endocrinology, Metabolism, and Infectious Diseases, Hirosaki University School of Medicine & Hospital, Hirosaki 036-8563, Japan

3. Family Medicine, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan

4. Aomori Rosai Hospital, Hachinohe 031-8551, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference53 articles.

1. 1. Newell-Price J, Besser M (2002) Evaluation of Cushing’s syndrome. In: Blevins LS (ed) Cushing’s syndrome. Kluwer academic publishers, Massachusetts: 71-97.

2. 2. Chihara K (2007) Guidance of diagnosis and treatment in Cushing’s disease. Reports 2006 on diencephalohypophyseal damage in Health and Labour Science Research: 130-132 (In Japanese).

3. 3. Suda T, Kageyama K, Nigawara T, Sakihara S (2009) Evaluation of diagnostic tests for ACTH-dependent Cushing’s syndrome. Endocr J 56: 469-476.

4. 4. Kageyama K, Oki T, Sakihara S, Nigawara T, Terui K, et al. (2013) Evaluation of the diagnostic criteria for Cushing’s disease in Japan. Endocr J 60: 127-135.

5. 5. Wade AN, Baccon J, Grady MS, Judy KD, O’Rourke DM, et al. (2011) Clinically silent somatotroph adenomas are common. Eur J Endocrinol 165: 39-44.

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