A Decrease in the Dose of Pegvisomant was Needed for the Treatment of Acromegaly after Adrenalectomy in a Patient with Coexisting Preclinical Cushing's Syndrome
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- Ogo Atsushi
- Department of Metabolism and Endocrinology, National Hospital Organization, Kyushu Medical Center, Japan
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- Matoba Yuka
- Department of Metabolism and Endocrinology, National Hospital Organization, Kyushu Medical Center, Japan
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- Matsuda Yayoi
- Department of Metabolism and Endocrinology, National Hospital Organization, Kyushu Medical Center, Japan
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- Hiramatsu Shinsuke
- Department of Metabolism and Endocrinology, National Hospital Organization, Kyushu Medical Center, Japan
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We herein describe the case of a 47-year-old woman with pre-clinical Cushing's syndrome caused by a left adrenal adenoma, which was diagnosed 6 years after trans-sphenoidal selective removal of a pituitary adenoma for acromegaly at age 35. The patient was started on bromocriptine and then somatostatin analogues after the surgery; however, since her serum insulin-like growth factor-1 (IGF-1) values remained above the age-adjusted normal range, the treatment for acromegaly was switched from somatostatin analogues to pegvisomant (10 mg daily), before a left laparoscopic adrenalectomy. After the subsequent adrenalectomy, the dose of pegvisomant could be reduced gradually to once every 4 days without any increase in the serum IGF-1 values. This is the first report describing the need for a different dose of pegvisomant for the treatment of acromegaly before and after adrenalectomy for pre-clinical Cushing's syndrome.<br>
収録刊行物
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- Internal Medicine
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Internal Medicine 50 (18), 1987-1991, 2011
一般社団法人 日本内科学会
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詳細情報 詳細情報について
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- CRID
- 1390001204871835008
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- NII論文ID
- 130000969309
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- ISSN
- 13497235
- 09182918
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- 使用不可