RSS-Feed abonnieren

DOI: 10.1055/s-0042-1758381
Rational Evaluation and Treatment of Prolactinomas: A Concise Review
Authors
Funding None.

Abstract
Prolactinoma is the most common pituitary tumor. It arises from the lactotroph cells and leads to a hyperprolactinemia state. The clinical presentation of prolactinomas is either due to the high prolactin state or the adenoma mass effect. Diagnosis of prolactinomas starts with the confirmation of persistent pathologic hyperprolactinemia. Subsequently, pituitary MRI is required to characterize the prolactinoma size and extension within the sella turcica. Further investigation may include visual field assessment and laboratory investigations for hypopituitarism. Prolactinoma management is mainly medical with dopamine agonists as most of these tumors are responsive. Surgical intervention is rarely required with specific indications.
Author's Contribution
Single author.
Compliance with Ethical Principles
Ethical approval was not required for the review article type of study.
Publikationsverlauf
Artikel online veröffentlicht:
02. Dezember 2022
© 2022. Gulf Association of Endocrinology and Diabetes (GAED). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
-
References
- 1 Bronstein MD. Disorders of prolactin secretion and prolactinomas. Endocrinology. United States: Elsevier; 2010: 333-357
- 2 Melmed S, Casanueva FF, Hoffman AR. et al; Endocrine Society. Diagnosis and treatment of hyperprolactinemia: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2011; 96 (02) 273-288
- 3 Fernandez A, Karavitaki N, Wass JA. Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK). Clin Endocrinol (Oxf) 2010; 72 (03) 377-382
- 4 Casanueva FF, Molitch ME, Schlechte JA. et al. Guidelines of the Pituitary Society for the diagnosis and management of prolactinomas. Clin Endocrinol (Oxf) 2006; 65 (02) 265-273
- 5 Beshyah SA, Sherif IH, Chentli F. et al. Management of prolactinomas: a survey of physicians from the Middle East and North Africa. Pituitary 2017; 20 (02) 231-240
- 6 Aldahmani KM, AlMalki MH, Beshyah SA. A rational approach to the evaluation and management of patients with hyperprolactinemia. Ibnosina J Med Biomed Sci 2020; 12: 90-97
- 7 Glezer ABM, In: Feingold KR, Anawalt B, Boyce A. et al., eds. Hyperprolactinemia. 2022
- 8 Maiter D, Delgrange E. Therapy of endocrine disease: the challenges in managing giant prolactinomas. Eur J Endocrinol 2014; 170 (06) R213-R227
- 9 Ignacak A, Kasztelnik M, Sliwa T, Korbut RA, Rajda K, Guzik TJ. Prolactin–not only lactotrophin. A “new” view of the “old” hormone. J Physiol Pharmacol 2012; 63 (05) 435-443
- 10 Vilar L, Fleseriu M, Bronstein MD. Challenges and pitfalls in the diagnosis of hyperprolactinemia. Arq Bras Endocrinol Metabol 2014; 58 (01) 9-22
- 11 Al Nuaimi A, Almazrouei R, Othman Y, Beshyah S, Aldahmani KM. Prevalence of Macroprolactinemia in patients with hyperprolactinemia using Roche Elecsys platform in a large tertiary referral center in UAE. Dubai Diab Endocrinol J 2021; 27 (04) 126-130
- 12 Che Soh NAA, Yaacob NM, Omar J. et al. Global prevalence of macroprolactinemia among patients with hyperprolactinemia: a systematic review and meta-analysis. Int J Environ Res Public Health 2020; 17 (21) 8199
- 13 Vilar L, Freitas MC, Naves LA. et al. Diagnosis and management of hyperprolactinemia: results of a Brazilian multicenter study with 1234 patients. J Endocrinol Invest 2008; 31 (05) 436-444
- 14 Kim JH, Hur KY, Hong SD. et al. Serum prolactin level to tumor size ratio as a potential parameter for preoperative differentiation of prolactinomas from hyperprolactinemia-causing non-functional pituitary adenomas. World Neurosurg 2022; 159: e488-e496
- 15 Leca BM, Mytilinaiou M, Tsoli M. et al. Identification of an optimal prolactin threshold to determine prolactinoma size using receiver operating characteristic analysis. Sci Rep 2021; 11 (01) 9801
- 16 Raverot V, Perrin P, Chanson P, Jouanneau E, Brue T, Raverot G. Prolactin immunoassay: does the high-dose hook effect still exist?. Pituitary 2022; 25 (04) 653-657
- 17 Petakov MS, Damjanović SS, Nikolić-Durović MM. et al. Pituitary adenomas secreting large amounts of prolactin may give false low values in immunoradiometric assays. The hook effect. J Endocrinol Invest 1998; 21 (03) 184-188
- 18 Webster J, Piscitelli G, Polli A, Ferrari CI, Ismail I, Scanlon MF. Cabergoline Comparative Study Group. A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. N Engl J Med 1994; 331 (14) 904-909
- 19 dos Santos Nunes V, El Dib R, Boguszewski CL, Nogueira CR. Cabergoline versus bromocriptine in the treatment of hyperprolactinemia: a systematic review of randomized controlled trials and meta-analysis. Pituitary 2011; 14 (03) 259-265
- 20 Huang HY, Lin SJ, Zhao WG, Wu ZB. Cabergoline versus bromocriptine for the treatment of giant prolactinomas: a quantitative and systematic review. Metab Brain Dis 2018; 33 (03) 969-976
- 21 Ma Q, Su J, Li Y. et al. The chance of permanent cure for micro-and macroprolactinomas, medication or surgery? A systematic review and meta-analysis. Front Endocrinol (Lausanne) 2018; 9: 636
- 22 Paepegaey AC, Salenave S, Kamenicky P. et al. Cabergoline tapering is almost always successful in patients with macroprolactinomas. J Endocr Soc 2017; 1 (03) 221-230
- 23 Souteiro P, Belo S, Carvalho D. Dopamine agonists in prolactinomas: when to withdraw?. Pituitary 2020; 23 (01) 38-44
- 24 Mallea-Gil MS, Manavela M, Alfieri A. et al. Prolactinomas: evolution after menopause. Arch Endocrinol Metab 2016; 60 (01) 42-46
- 25 Santharam S, Fountas A, Tampourlou M. et al. Impact of menopause on outcomes in prolactinomas after dopamine agonist treatment withdrawal. Clin Endocrinol (Oxf) 2018; 89 (03) 346-353
- 26 Zou Y, Li D, Gu J. et al. The recurrence of prolactinoma after withdrawal of dopamine agonist: a systematic review and meta-analysis. BMC Endocr Disord 2021; 21 (01) 225
- 27 Espinosa-Cárdenas E, Sánchez-García M, Ramírez-Rentería C, Mendoza-Zubieta V, Sosa-Eroza E, Mercado M. High biochemical recurrence rate after withdrawal of cabergoline in prolactinomas: is it necessary to restart treatment?. Endocrine 2020; 70 (01) 143-149
- 28 Buchfelder M, Zhao Y, Schlaffer SM. Surgery for prolactinomas to date. Neuroendocrinology 2019; 109 (01) 77-81
- 29 Kreutzer J, Buslei R, Wallaschofski H. et al. Operative treatment of prolactinomas: indications and results in a current consecutive series of 212 patients. Eur J Endocrinol 2008; 158 (01) 11-18
- 30 Frara S, Rodriguez-Carnero G, Formenti AM, Martinez-Olmos MA, Giustina A, Casanueva FF. Pituitary tumors centers of excellence. Endocrinol Metab Clin North Am 2020; 49 (03) 553-564
- 31 Raverot G, Burman P, McCormack A. et al; European Society of Endocrinology. European Society of Endocrinology Clinical Practice Guidelines for the management of aggressive pituitary tumours and carcinomas. Eur J Endocrinol 2018; 178 (01) G1-G24
- 32 Huang W, Molitch ME. Pituitary tumors in pregnancy. Endocrinol Metab Clin North Am 2019; 48 (03) 569-581
- 33 Lebbe M, Hubinont C, Bernard P, Maiter D. Outcome of 100 pregnancies initiated under treatment with cabergoline in hyperprolactinaemic women. Clin Endocrinol (Oxf) 2010; 73 (02) 236-242
- 34 Hurault-Delarue C, Montastruc JL, Beau AB, Lacroix I, Damase-Michel C. Pregnancy outcome in women exposed to dopamine agonists during pregnancy: a pharmacoepidemiology study in EFEMERIS database. Arch Gynecol Obstet 2014; 290 (02) 263-270