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Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Pituitary tumours: the prolactinoma
1Department of Molecular and Clinical Endocrinology and Oncology, Federico II University, via S. Pansini 5, 80131 Naples, Italy. colao@unina.it
Best Practice & Research. Clinical Endocrinology & Metabolism
|December 1, 2009
Summary
Prolactinomas are more common than previously thought. Lifelong treatment with dopamine agonists is often necessary, but some patients may achieve lasting remission after stopping medication.
Area of Science:
- Endocrinology
- Oncology
Background:
- Prolactinomas, pituitary tumors secreting prolactin (PRL), exhibit a higher prevalence than previously estimated.
- Diagnostic criteria for hyperprolactinemia have been streamlined, primarily relying on PRL assays and sellar MRI.
Purpose of the Study:
- To review the epidemiology, diagnosis, and treatment of prolactinomas.
- To highlight recent findings on prolactinoma prevalence and management strategies.
Main Methods:
- Literature review focusing on epidemiology, diagnostic advancements, and therapeutic outcomes for prolactinomas.
- Analysis of recent data on tumor prevalence and patient response to medical therapy.
Main Results:
- The prevalence of prolactinomas is significantly underestimated, potentially 3-5 times higher than earlier reports.
- Macroprolactinaemia requires assessment in asymptomatic hyperprolactinemia cases.
- Long-term dopamine agonist therapy is supported by current evidence.
- Tumor disappearance and normalized PRL levels during treatment correlate with persistent remission post-withdrawal.
Conclusions:
- Prolactinoma diagnosis and management have evolved, with increased awareness of prevalence.
- Dopamine agonist therapy remains a cornerstone, with predictors for sustained remission identified.
- Further research into long-term treatment outcomes and remission criteria is warranted.
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