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Acromegaly secondary to growth hormone releasing hormone secretion
1Department of Endocrinology, James Connolly Memorial Hospital, Dublin, Ireland. amaragha@yahoo.com
Background:
Acromegaly secondary to growth hormone releasing hormone (GHRH) secretion is exceptionally rare.
Aim:
To report a case of acromegaly diagnosed in 1984 and assumed to be pituitary in origin. Sixteen years later, the cause was found to be a GHRH secreting neuroendocrine pancreatic tumour.
Method:
A case report.
Conclusion:
Although ectopic GHRH production is very rare, endocrinologists should be aware of this possibility in acromegaly patients if a pituitary tumour was not detected using pituitary imaging.
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