Abstract
We report a rare case of polycystic ovary syndrome (PCOS) complicated with acromegaly due to a growth hormone (GH)-producing pituitary adenoma. Complete removal of the pituitary adenoma successfully reduced circulating levels of GH and insulin-like growth factor (IGF)-l, which, in turn, resulted in the amelioration of gonadal dysfunction, hyperandrogenism, lutenizing hormone hypersecretion, and severe insulin resistance. This clinical complication suggests that activation of systemic GH-IGF-1 axis is potentially involved in the development of PCOS.
Original language | English |
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Pages (from-to) | 157-160 |
Number of pages | 4 |
Journal | Endocrine journal |
Volume | 56 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2009 |
Keywords
- Acromegaly
- Growth hormone
- Hyperglycemia
- Insulin-like growth factor-1
- Polycystic ovary syndrome
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Endocrinology