Acromegaly — SCE Endocrinology MCQ
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Correct answer: A — Acromegaly from a pituitary somatotroph adenoma
Raised IGF-1 with failure of GH suppression during OGTT confirms acromegaly, and a pituitary microadenoma is the common cause. Pseudoacromegaly has clinical features without biochemical GH excess. The pearl is that random GH is unreliable; suppression testing is key.
Reference: Endocrine Society acromegaly guideline, Society for Endocrinology guidance