Prolactinoma surgery: Difference between revisions
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Revision as of 19:32, 16 October 2017
Prolactinoma Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Prolactinoma surgery On the Web |
American Roentgen Ray Society Images of Prolactinoma surgery |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Faizan Sheraz, M.D. [2], Anmol Pitliya, M.B.B.S. M.D.[3]
Overview
Surgery is not the first-line treatment option for patients with prolactinoma. Surgery is usually reserved for patients in whom medical therapy fails to reduce the size of the tumor.
Surgery
Indications
Medical therapy should be continued even if it is partially successful, possibly combined with surgery or radiation. Surgery is indicated in patients if medical therapy:[1][2][3]
- Cannot be tolerated
- Fails to reduce prolactin concentration
- Fails to restore normal reproductive and pituitary function
- Fails to reduce tumor size
Transsphenoidal resection
Usually, the tumor is removed through the nasal cavity. Rarely, if the tumor is large or has spread to nearby brain tissue, the surgeon will access the tumor through an opening in the skull. The results of surgery depend on tumor size and prolactin concentrations. Surgery corrects prolactin concentrations in approximately 80% of patients with:
References
- ↑ "Prolactinoma | NIDDK".
- ↑ Colao A, Savastano S (2011). "Medical treatment of prolactinomas". Nat Rev Endocrinol. 7 (5): 267–78. doi:10.1038/nrendo.2011.37. PMID 21423245.
- ↑ Nomikos P, Buchfelder M, Fahlbusch R (2001). "Current management of prolactinomas". J Neurooncol. 54 (2): 139–50. PMID 11761431.