Background
By definition, a microadenoma (seen in the image below) is a tumor less than 10 mm in diameter. Pituitary adenomas may secrete hormones, or they may be clinically inactive. Many pituitary lesions are discovered while investigating other neurologic problems; these lesions are called incidentalomas.
MRI showing a nonenhancing area in the pituitary consistent with a microadenoma in a patient with hyperprolactinemia. Pathophysiology
Of the secretory tumors, the most common are prolactinomas. Other secretory tumors may secrete (1) adrenocorticotrophic hormone (ACTH), causing Cushing disease; (2) growth hormone, causing acromegaly; (3) gonadotropins with clinical presentations reflective of severity and sex; or, rarely, (4) thyroid-stimulating hormone (TSH), causing hyperthyroidism. Many secrete inactive alpha-subunits of the glycoprotein hormones. Most incidentalomas are inactive and are of no clinical consequence. As with adenomas in other endocrine glands, all these tumors probably derive from a local mutation, with loss of function of the genes controlling cell proliferation.
The role of genetic mutations was highlighted in a report suggesting that patients with pituitary tumors from 4 Irish families share a common mutation with a patient from the 18th century who had pituitary tumor–mediated gigantism.[1]
Epidemiology
Frequency
United States
A high-resolution magnetic resonance imaging (MRI) screen of a normal population has shown a 10% prevalence of pituitary lesions.
International
In studies with a total of 10,370 autopsies, the prevalence of pituitary microadenomas was 11%; however, in a Japanese series of 1000 autopsies, many of the midline pituitary lesions were Rathke cysts, not adenomas.
Mortality/Morbidity
Microadenomas do not cause directly attributable excess mortality. These tumors generally are too small to cause bony erosion or to put pressure on the optic chiasm. Any morbidity is caused by excessive hormone secretion.
Race
No race predilection exists.
Sex
Microadenomas may occur in either sex. Prolactinomas are diagnosed more frequently in women, possibly because of the more striking presenting features such as amenorrhea and/or galactorrhea. In men, the diagnosis of inactive adenomas is often delayed until they have become macroadenomas and cause mass effects.
Age
Microadenomas may occur at any age, but prevalence appears to increase with advancing age.
Chahal HS, Stals K, Unterländer M, Balding DJ, Thomas MG, Kumar AV, et al. AIP mutation in pituitary adenomas in the 18th century and today. N Engl J Med. Jan 6 2011;364(1):43-50. [Medline].
Bush ZM, Lopes MB, Hussaini IM, et al. Immunohistochemistry of COUP-TFI: an adjuvant diagnostic tool for the identification of corticotroph microadenomas. Pituitary. Jun 13 2009;[Medline].
Suda T, Kageyama K, Nigawara T, et al. Evaluation of diagnostic tests for ACTH-dependent Cushing's syndrome. Endocr J. Jun 2009;56(3):469-76. [Medline]. [Full Text].
Macchia E, Gasperi M, Lombardi M, et al. Clinical aspects and therapeutic outcome in TSH-secreting pituitary adenomas: a single center experience. J Endocrinol Invest. Jul 28 2009;[Medline].
Fleseriu M, Yedinak C, Campbell C, et al. Significant headache improvement after transsphenoidal surgery in patients with small sellar lesions. J Neurosurg. Feb 2009;110(2):354-8. [Medline].
Ono M, Miki N, Kawamata T, et al. Prospective study of high-dose cabergoline treatment of prolactinomas in 150 patients. J Clin Endocrinol Metab. Dec 2008;93(12):4721-7. [Medline].
Fernandez-Balsells MM, Murad MH, Barwise A, et al. Natural history of nonfunctioning pituitary adenomas and incidentalomas: a systematic review and metaanalysis. J Clin Endocrinol Metab. Apr 2011;96(4):905-12. [Medline].
Aron DC, Howlett TA. Pituitary incidentalomas. Endocrinol Metab Clin North Am. Mar 2000;29(1):205-21. [Medline].
Bailey RH, Aron DC. The diagnostic dilemma of incidentalomas. Working through uncertainty. Endocrinol Metab Clin North Am. Mar 2000;29(1):91-105. [Medline].
Boni G, Ferdeghini M, Bellina CR, et al. [111In-DTPA-D-Phe]-octreotide scintigraphy in functioning and non-functioning pituitary adenomas. Q J Nucl Med. Dec 1995;39(4 Suppl 1):90-3. [Medline].
Cannavo S, De Natale R, Curto L, et al. Effectiveness of computer-assisted perimetry in the follow-up of patients with pituitary microadenoma responsive to medical treatment. Clin Endocrinol (Oxf). Aug 1992;37(2):157-61. [Medline].
de Herder WW, Uitterlinden P, Pieterman H, et al. Pituitary tumour localization in patients with Cushing's disease by magnetic resonance imaging. Is there a place for petrosal sinus sampling?. Clin Endocrinol (Oxf). Jan 1994;40(1):87-92. [Medline].
De Rosa M, Zarrilli S, Di Sarno A, et al. Hyperprolactinemia in men: clinical and biochemical features and response to treatment. Endocrine. Feb-Mar 2003;20(1-2):75-82. [Medline].
Galluzzi F, Salti R, et al. Reversible weight gain and prolactin levels--long-term follow-up in childhood. J Pediatric Endocrinology. Sep 2005;18(9(:921-4. [Medline].
Karam K, Sayegh R, Saadeh G, Saba M. Gonadotropin secreting pituitary microadenoma. J Med Liban. 1992;40(1):31-5. [Medline].
King JT, Justice AC, Aron DC. Management of incidental pituitary microadenomas: a cost-effectiveness analysis. J Clin Endocrinol Metab. Nov 1997;82(11):3625-32. [Medline].
Losa M, Mortini P, Barzaghi R, et al. Surgical treatment of prolactin-secreting pituitary adenomas: early results and long-term outcome. J Clin Endocrinol Metab. Jul 2002;87(7):3180-6. [Medline].
Maruyama T, Masuda H, Uchida H, Nagashima T, Yoshimura Y. Follicle stimulating hormone-secreting pituitary microadenoma with fluctuating levels of ovarian hyperstimulation. Obstet Gynecol. May 2005;105(5 Pt 2):1215-8. [Medline].
Minniti G, Jaffrain-Rea ML, Esposito V, et al. Evolving criteria for post-operative biochemical remission of acromegaly: can we achieve a definitive cure? An audit of surgical results on a large series and a review of the literature. Endocr Relat Cancer. Dec 2003;10(4):611-9. [Medline].
Molitch ME. Management of prolactinomas during pregnancy. J Reprod Med. Dec 1999;44(12 Suppl):1121-6. [Medline].
Oruckaptan HH, Senmevsim O, Ozcan OE, Ozgen T. Pituitary adenomas: results of 684 surgically treated patients and review of the literature. Surg Neurol. Mar 2000;53(3):211-9. [Medline].
Park YG, Chang JW, Kim EY, Chung SS. Gamma knife surgery in pituitary microadenomas. Yonsei Med J. Jun 1996;37(3):165-73. [Medline].
Ricci G, Giolo E, Nucera G et al. Pregnancy in hyperprolactinemic infertile women treated with vaginal bromocripptine: report of two cases and review of the literature. Gynecologic and Obstetric Investigation. 2001;51(4):266-70. [Medline].
Shimon I, Ram Z, Cohen ZR, Hadani M. Transsphenoidal surgery for Cushing's disease: endocrinological follow-up monitoring of 82 patients. Neurosurgery. Jul 2002;51(1):57-61; discussion 61-2. [Medline].
Simard MF. Pituitary tumor endocrinopathies and their endocrine evaluation. Neurosurg Clin N Am. Jan 2003;14(1):41-54, vi. [Medline].
Teramoto A, Hirakawa K, Sanno N, Osamura Y. Incidental pituitary lesions in 1,000 unselected autopsy specimens. Radiology. Oct 1994;193(1):161-4. [Medline].
Tripathi S, Ammini AC, Bhatia R, et al. Cushing's disease: pituitary imaging. Australas Radiol. Aug 1994;38(3):183-6. [Medline].
Verhelst J, Abs R, Maiter D, et al. Cabergoline in the treatment of hyperprolactinemia: a study in 455 patients. J Clin Endocrinol Metab. Jul 1999;84(7):2518-22. [Medline].
Xu RK, Wu XM, Di AK, et al. Pituitary prolactin-secreting tumor formation: recent developments. Biol Signals Recept. Jan-Feb 2000;9(1):1-20. [Medline].

