Best Practice & Research Clinical Endocrinology & Metabolism
Volume 23, Issue 5 , Pages 667-675, October 2009

Pituitary incidentalomas

  • Mark E. Molitch, MD (Professor of Medicine)

      Affiliations

    • Corresponding Author InformationTel.: +1 312 503 4130; Fax: +1 312 926 8693.

Division of Endocrinology, Metabolism and Molecular Medicine, Northwestern University Feinberg School of Medicine, 645 N. Michigan Avenue, Suite 530, Chicago, IL 60611, USA

Clinically non-functioning pituitary adenomas range from being completely asymptomatic, and therefore being detected either at autopsy or as incidental findings on head magnetic resonance imaging (MRI) or computed tomography (CT) scans performed for other reasons (often referred to as ‘pituitary incidentalomas'), to causing significant hypothalamic/pituitary dysfunction and visual field compromise due to their large size. Patients with pituit-ary incidentalomas should all be screened for hypersecretion (prolactin (PRL), IGF-1, midnight salivary cortisol), and those with macroadenomas should also be screened for hypopituitarism (macroadenomas) and for visual field defects if the tumour abuts the optic chiasm. Growth of non-functioning pituitary adenomas without treatment occurs in about 10% of microadenomas and 24% of macroadenomas. In the absence of hypersecretion, hypopituitarism or visual field defects, patients may be followed up by periodic screening by MRI for enlargement. Growth of a pituitary incidentaloma is an indication for surgery.

Keywords: adenoma, pituitary, incidentaloma, tumour, trans-sphenoidal surgery

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PII: S1521-690X(09)00048-7

doi:10.1016/j.beem.2009.05.001

Best Practice & Research Clinical Endocrinology & Metabolism
Volume 23, Issue 5 , Pages 667-675, October 2009