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Review article| Volume 92, P143-149, October 2016

Pituitary incidentalomas: A guide to assessment, treatment and follow-up

  • Stavroula Α. Paschou
    Affiliations
    Unit of Reproductive Endocrinology, First Department of Obstetrics and Gynecology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece

    Department of Endocrinology and Diabetes, Hellenic Red Cross Hospital, Athens, Greece
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  • Andromachi Vryonidou
    Affiliations
    Department of Endocrinology and Diabetes, Hellenic Red Cross Hospital, Athens, Greece
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  • Dimitrios G. Goulis
    Correspondence
    Corresponding author at: Unit of Reproductive Endocrinology, First Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, “Papageorgiou” General Hospital, Ring Road, Nea Efkarpia, Thessaloniki 56403, Greece.
    Affiliations
    Unit of Reproductive Endocrinology, First Department of Obstetrics and Gynecology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece
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      Highlights

      • Pituitary incidentalomas are lesions which are detected incidentally during imaging procedures for unrelated causes.
      • Micro-incidentalomas (less than 1 cm in size) have a reported mean prevalence in normal individuals of around 10%.
      • The endocrinologist facing a pituitary incidentaloma has to solve two main diagnostic problems: the nature and extent of the lesion, and the hormonal excess or deficits resulting from this lesion.
      • Visual deficits or neurological disturbances due to compression of the optic chiasm or nerve by the incidentaloma are the strongest recommendations for surgery.
      • Hormonally active incidentalomas, with the exception of prolactinomas, should be also treated by surgery.

      Abstract

      Pituitary incidentalomas are lesions which are detected incidentally in the pituitary gland during imaging procedures for unrelated causes, such as headache, trauma or symptoms involving the neck or central nervous system. The wide application of sensitive brain imaging techniques (CT, MRI) has led to an increasing recognition of such lesions. Although the etiology of pituitary incidentalomas covers a wide range of pathologies, most of them (∼90%) are benign adenomas; nonetheless, they may result in visual and/or neurologic abnormalities. By definition, micro-incidentalomas have maximum diameter of less than 1 cm, while macro-incidentalomas are at least 1 cm. Micro-incidentalomas have a reported mean prevalence in normal individuals of around 10%. The endocrinologist facing a pituitary incidentaloma has to solve two main diagnostic problems: (i) the nature and extent of the lesion, and (ii) whether hormonal excess or deficits result from the lesion. The former is achieved by the use of pituitary MRI and visual field (VF) examination and the latter by basal or dynamic hormonal assessments. The answers to these two questions will guide the treatment and follow-up. VF deficits or neurological disturbances due to compression of the optic chiasm or nerve by the incidentaloma are the strongest recommendations for surgery. Furthermore, hormonally active incidentalomas, with the exception of prolactinomas, should be treated by surgery. Most cases of pituitary incidentalomas do not meet criteria for surgical excision, but may require follow-up. The follow-up strategy consists of clinical evaluation, pituitary MRI, VF examination and hormonal assessments. Macro-incidentalomas require more extensive initial investigation, as well as closer MRI surveillance, than micro-incidentalomas. Diagnostic, treatment and follow-up strategies should be in alignment with the optimal personalized clinical benefit.

      Abbreviations:

      α-SU (α-subunits), ACTH (adrenocorticotropic hormone), CN (cranial nerve), CT (computed tomography), FSH (follicle-stimulating hormone), Gd (gadolinium), GH (growth hormone), LH (luteinizing hormone), MRI (magnetic resonance imaging), PRL (prolactin), TSH (thyroid stimulating hormone), VF (visual field)

      Keywords

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