Background: Paediatric pituitary adenomas are rare intracranial neoplasms that can manifest clinically as neurological symptoms or endocrine disorder due to mass effect and/or disruption of hormone secretion. Current treatment options for pituitary adenomas include medical management with pharmacologic agents, surgical resection and radiation therapy. In this report we examine a case of pituitary macroadenoma secondary to primary hypothyroidism.
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Ryan et al. (2024) studied this question.
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