AffiliationAcademic Department of Endocrinology, Beaumont Hospital, Dublin 9, Ireland, email@example.com.
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CitationAcromegaly associated with gangliocytoma. 2009: Ir J Med Sci
JournalIrish journal of medical science
AbstractBACKGROUND: Acromegaly secondary to growth hormone-releasing hormone (GHRH) excess is rare. AIMS/CASE DESCRIPTION: We report two patients with acromegaly who were diagnosed with sellar gangliocytomas that were immunopositive for GHRH. Tumour tissue persisted after debulking surgery and in the second case this was associated with persistent growth hormone hypersecretion, successfully suppressed by a somatostatin analogue. CONCLUSIONS: The development of functional pituitary adenomas in association with sellar gangliocytomas is poorly understood. We present a brief discussion of the possible aetiology of these unusual pituitary tumours.
Item TypeArticle In Press