Best Practice & Research Clinical Endocrinology & Metabolism
Volume 23, Issue 5 , Pages 575-596, October 2009

The prolactinoma

  • Annamaria Colao, MD, PhD (Professor of Endocrinology)

      Affiliations

    • Corresponding Author InformationTel.: +39 81 7462132; Fax: +39 81 7463668.

Department of Molecular and Clinical Endocrinology and Oncology, “Federico II” University, via S. Pansini 5, 80131 Naples, Italy

This review focusses on the epidemiology, diagnosis and treatment of prolactinomas. In particular, attention was given to recent data showing a high prevalence of these tumours in the general population, 3–5 times higher than previously reported. The diagnosis of hyperprolactinaemia has been simplified in recent years, and only prolactin (PRL) assay and magnetic resonance imaging of the sella are required. Nonetheless, macroprolactinaemia should be assessed in patients with hyperprolactinaemia in the absence of clinical symptoms of elevated PRL levels. The recent evidence that medical therapy with dopamine agonists should be continued lifelong has been confirmed by several studied. The patients achieving disappearance of the tumours and suppression of PRL levels during treatment are those showing the highest likelihood to have persistent remission of hyperprolactinaemia after treatment withdrawal.

Keywords: prolactinomas, medical therapy, dopamine agonists, bromocriptine, cabergoline, quinagolide, surgery, radiotherapy

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PII: S1521-690X(09)00047-5

doi:10.1016/j.beem.2009.05.003

Best Practice & Research Clinical Endocrinology & Metabolism
Volume 23, Issue 5 , Pages 575-596, October 2009