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Review

Incidentally discovered pituitary masses: pituitary incidentalomas

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Pages 253-264 | Published online: 10 Jan 2014

References

  • Tenner E. Why Things Bite Back: Technology and the Revenge of Unintended Consequences. Knopf AA (Ed.) NY, USA (1996).
  • Chidiac RM, Aron DC. Incidentalomas: a disease of modern technology. Endocrinol. Metab. Clin. N. Am.26, 233–253 (1997).
  • Lau J, Balk E, Rothberg M et al. Management of clinically inapparent adrenal mass. Evidence Report/Technology Assessment (number 56). AHRQ Publication Rockville, MD, USA (2002).
  • Molitch ME, Russell EJ. The pituitary “incidentaloma”. Ann. Intern. Med.112, 925–931 (1990).
  • Molitch M. Non functioning pituitary tumors and pituitary incidentalomas. Endocrinol. Metab. Clin. N. Am.37, 151–171 (2008).
  • Serhal D, Weil R, Hamrahian A. Evaluation and management of pituitary incidentalomas. Cleve. Clin. J. Med.75, 793–801 (2008).
  • Klibanski A, Zervas NT, Kovacs K, Ridgeway EC. Clinically silent hypersecretion of growth hormone in patients with pituitary tumors. J. Neurosurg.66, 806–811 (1987).
  • Aron DC. The adrenal incidentaloma: disease of modern technology and public health problem. Rev. Endocr. Metab. Disord.2, 335–342 (2001).
  • Aron DC. Endocrine incidentalomas. Endocrinol. Metab. Clin. North Am.29, 1–238 (2002).
  • King JT Jr, Justice A, Aron DC. Management of incidental pituitary microadenomas: a cost-effectiveness analysis. J. Clin. Endocrinol. Metab.82, 3625–3632 (1997).
  • Krikorian A, Aron DC. Pituitary incidentalomas: revisiting an old acquaintance. Endocrinol. Metab. Clin. North Am.2, 1–8 (2006).
  • Mavrakis A, Tritos N. Diagnostic and therapeutic approach to pituitary incidentalomas. Endocr. Pract.10, 438–444 (2004).
  • Howlett TA, Como J, Aron DC. Management of pituitary incidentalomas. A survey of British and American endocrinologists. Endocrinol. Metab. Clin. N. Am.29, 223–230 (2000).
  • Molitch M. Clinical review 65 evaluation and treatment of the patient with a pituitary incidentaloma. J. Clin. Endocrinol. Metab.80, 3–6 (1995).
  • Sam S, Molitch M. The pituitary mass: diagnosis and management. Rev. Endocr. Metab. Disord.6, 55–62 (2005).
  • Teramoto A, Hirakawa K, Sanno N, Osamura Y. Incidental pituitary lesions in 1,000 unselected autopsy specimens. Radiology193, 161–164 (1994).
  • Ezzat S, Asa SL, Couldwell WT et al. The prevalence of pituitary adenomas: a systematic review. Cancer101(3), 613–619 (2004).
  • Rittierodt M, Hori A. Pre-morbid morphological conditions of the human pituitary. Neuropathology27, 43–48 (2007).
  • Nammour G, Ybarra J, Naheedy M, Romeo J, Aron D. Incidental pituitary macroadenoma: a population-based study. Am. J. Med. Sci.314, 287–291 (1997).
  • Vernooij M, Ikram M, Tanghe H, Vincent A. Incidental findings on brain MRI in the general population. N. Engl. J. Med.357, 1821–1828 (2007).
  • Yue NC Longstreth WT Jr, Elster AD et al. Clinically serious abnormalities found incidentally at MR imaging of the brain: data from the Cardiovascular Health Study. Radiology202, 41–46 (1997).
  • Wolpert S, Molitch M, Goldman J, Wood J. Size, shape, and appearance of the normal female pituitary gland. Am. J. Roentgenol.143, 377–381 (1984).
  • Hall WA, Luciano MG, Doppman JL, Patronas NJ, Oldfield EH. Pituitary magnetic resonance imaging in normal human volunteers: occult adenomas in the general population. Ann. Intern. Med.120, 817–820 (1994).
  • Gao R, Isoda H, Tanaka T et al. Dynamic gadolinium-enhanced MR imaging of pituitary adenomas: usefulness of sequential sagittal and coronal plane images. Eur. J. Radiol.39, 139–146 (2001).
  • Indrajit ICN, Sundar K, Ahmed I. Value of dynamic MRI imaging in pituitary adenomas. Ind. J. Radiol. Imag.11, 185–190 (2001).
  • Arita K, Tominaga A, Sugiyama K et al. Natural course of incidentally found nonfunctioning pituitary adenoma, with special reference to pituitary apoplexy during follow up examination. J. Neurosurg.104, 884–891 (2006).
  • Johnson MD, Woodburn CJ, Vance M. Quality of life in patients with a pituitary adenoma. Pituitary6, 81–87 (2003).
  • Karavitaki N, Collison K, Halliday J et al. What is the natural history of nonoperated nonfunctioning pituitary adenomas? Clin. Endocrinol.67, 938–943 (2007).
  • Cury M, Fernandes J, Machado H et al. Non-functioning pituitary adenomas: clinical feature, laboratorical and imaging assessment, therapeutic management and outcome. Arq. Bras. Endocrinol. Metab.53, 31–39 (2008).
  • Dekkers O, Hammick M, de Keizer R et al. The natural course of non-functioning pituitary macrodenomas. Eur. J. Endocrinol.156, 217–224 (2007).
  • Fainstein Day P, Guitelman M, Artese R et al. Retrospective multicentric study of pituitary incidentalamos. Pituitary7, 145–148 (2004).
  • Kastelan D, Korsic M. High prevalence rate of pituitary incidentaloma: is it associated with the age-related decline of the sex hormones levels? Medical Hypotheses69, 307–309 (2007).
  • Ciccarelli A, Daly A, Beckers A. The epidemiology of prolactinomas. Pituitary8, 3–6 (2005).
  • Coulter I, Mukerji N, Bradey N, Connolly V, Kane P. Radiologic follow-up of non-functioning pituitary adenomas: rationale and cost effectiveness. J. Neurooncol.93, 157–163 (2009).
  • Turner H, Stratton I, Byrne J, Adams C, Wass J. Audit of selected patients with nonfunctioning pituitary adenomas treated without irradiation – a follow-up study. Clin. Endocrinol.51, 281–284 (1999).
  • Donovan L, Corenblum B. The natural history of the pituitary incidentaloma. Arch. Intern. Med.155, 181–183 (1995).
  • Reincke M, Allolio B, Saeger W, Menzel J, Winkelmann W. The ‘incidentaloma’ of the pituitary gland. Is neurosurgery required. JAMA263, 2772–2776 (1990).
  • Freda P, Post K. Differential diagnosis of sellar masses. Endocrinol. Metab. Clin. N. Am.28, 81–117 (1995).
  • Ambrosi B, Faglia G; the Multicenter Pituitary Tumor Study Group. Lombardia region. Epidemiology of pituitary tumors. Pituitary adenomas In: New Trends in Basic and Clinical Research. Faglia G, Beck-Peccoz P, Ambrosi B, Travaglini P, Spada A (Eds).Elsevier Science Publishers, NY, USA 159–168 (1991).
  • Daly A, Rixhon M, Adam C et al. High prevalence of pituitary adenomas: a cross-sectional study in the province of Liège, Belgium. J. Clin. Endocrinol. Metab.91, 4769–4775 (2006).
  • Golden S, Robinson K, Saldanha I, Anton B, Ladenson P. Prevalence and incidence of endocrine and metabolic disorders in the United States: a comprehensive review. J. Clin. Endocrinol. Metab.94, 1853–1878 (2009).
  • Sakharova A, Dimaraki E, Chandler W, Barkan AL. Clinically silent somatotropinomas may be biochemically active. J. Clin. Endocrinol. Metab.90, 2117–2121 (2005).
  • Yuen K, Cook D, Sahasranam P et al. Prevalence of GH and other pituitary hormone deficiencies in adults with nonsecreting pituitary microadenomas and normal serum IGF-1 levels. Clin. Endocrinol.69, 292–298 (2008).
  • Oyama K, Sanno N, Tahara S, Teramot A. Management of pituitary incidentalomas: according to a survey of pituitary incidentalomas in Japan. Semin. Ultrasound CT MR26, 47–50 (2005).
  • Miyai K, Icinhare K, Kondo K, Nomi S. Asymptomatic hyperprolactinaemia and prolactinaemia in the general population. Mass screening by paired assays of serum prolactin. Clin. Endocrinol.25, 549–554 (1986).
  • Miyake A, Ikegami M, Chen CF et al. Mass screening for hyperprolactinemia and prolactinoma in men. J. Endocrinol. Investig.11, 383–384 (1988).
  • Randall RV, Laws ER Jr, Abboud CF, Ebersold MJ, Kao PC, Scheithauer BW. Transsphenoidal microsurgical treatment of prolactin-producing pituitary adenomas. Results in 100 patients. Mayo Clin. Proc.58, 108–121 (1983).
  • Shy KK, McTiernan AM, Daling JR, Weiss NS. Oral contraceptive use and the occurrence of pituitary prolactinoma. J. Am. Med. Assoc.249, 2204–2207 (1983).
  • Annegers JF, Coulam CB, Abboud CF, Laws ER Jr, Kurland LT. Pituitary adenoma in Olmstead County, Minnesota, 1935–1977: a report of an increasing incidence of diagnosis in women of childbearing age. Mayo Clin. Proc.53, 641–643 (1978).
  • Alexander L, Appleton D, Hall R, Ross WM, Wilkinson R. Epidemiology of acromegaly in the Newcastle region. Clin. Endocrinol.12, 71–79 (1980).
  • Bengtsson BA, Eden S, Ernest I et al. Epidemiology and long-term survival in acromegaly. Acta Med. Scand.223, 327–335 (1988).
  • Schneider HJ, Sievers C, Saller B, Wittchen HU, Stalla GK. High prevalence of biochemical acromegaly in primary care patients with elevated IGF-1 levels. Clin. Endocrinol. (Oxford)69, 432–435 (2008).
  • Demura H, Takeda R, Miyamori I et al. Cushing’s syndrome in Japan with special reference to adrenocortical nodular dysplasia or hyperplasia. Controversies in Disorders of Adrenal Hormones: Proceedings of the Open Symposium of Disorders of Adrenal Hormone. Takeda R, Miyamori I (Eds). Excerpta Medica Tokyo, Japan, Amsterdam, The Netherlands 3–25 (1988).
  • Extabe J, Vazquez JA. Morbidity and mortality in Cushing’s disease: an epidemiological approach. Clin. Endocrinol.40, 479–484 (1994).
  • Lindholm J, Jujul S, Jørgensen J et al. Incidence and late prognosis of Cushing’s syndrome: a population-based study. J. Clin. Endocrinol. Metab.86, 117–123 (2001).
  • Daneshdoost L, Gennarelli TA, Bashey HM et al. Identification of gonadotroph adenomas in men with clinically nonfunctioning adenomas by the luteinizing hormone subunit response to thyrotropin-releasing hormone. J. Clin. Endocrinol. Metab.77, 1352–1355 (1993).
  • Oppenheim DS, Kana AR, Sangha JS, Klibanski A. Prevalence of α-subunit hypersecretion in patients with pituitary tumors: clinically non-functioning and somatotroph adenomas. J. Clin. Endocrinol. Metab.70, 859–864 (1990).
  • Buurman H, Saeger W. Subclinical adenomas in postmortem pituitaries: classification and correlation to clinical data. Eur. J. Endocrinol.154, 753–758 (2006).
  • Feldkamp Jm Santen R, Harms E et al. Incidentally discovered pituitary lesions: high frequency of macroadenomas and hormone-secreting adenomas – results of a prospective study. Clin. Endoccrinol. (Oxford)51, 109–113 (1999).
  • Nishizawa S, Ohto S, Yokoyama T, Uemura K. Therapeutic strategy for incidentally found pituitary tumors (“pituitary incidentalomas”). Neurosurgery43, 1344–1348 (1998).
  • Sanno N, Oyama K, Tahara S, Teramoto A, Kato Y. A survey of pituitary incidentaloma in Japan. Endocrinology149, 123–127 (2003).
  • Wass J, Karavitaki N. Nonfunctioning pituitary adenomas: the Oxford experience. Nat. Rev. Endocrinol.5, 519–522 (2009).
  • Honegger J, Zimmermann S, Psaras T et al. Growth modelling of non-functioning pituitary adenomas in patients refered for surgery. Eur. J. Endocrinol.158, 287–294 (2008).
  • Davis P, Hoffman J, Tindall G, Braun I. CT surgical correlation in pituitary adenomas: evaluation in 113 patients. Am. J. Neuroradiol.6, 711–716 (1985).
  • Johnson M, Hoare RD, Cox T et al. The evaluation of patients with a suspected pituitary microadenoma: computer tomography approximately magnetic resonance imaging. Clin. Endocrinol. (Oxford)36, 335–338 (1992).
  • Kulkarni M, Lee K, McArdle C et al. MR imaging of pituitary microadenomas: technical considerations and CT correlation. Am. J. Neuroradiol.9, 5–11 (1988).
  • Connor S, Penney C. MRI in the differential diagnosis of a sellar mass. Clin. Radiol.58, 20–31 (2003).
  • Kaltsas G, Nomikos P, Kontogeorgos G, Buchfelder M, Grossman A. Clinical review: diagnosis and management of pituitary carcinomas. J. Clin. Endocrinol. Metab.90, 3089–3099 (2005).
  • Webb S, Ruscalleda J, Schwarzstein D et al. Computerized tomography versus magnetic resonance imaging: a comparative study in hypothalamic-pituitary and parasellar pathology. Clin. Endocrinol. (Oxford)36, 465 (1992).
  • Aron DC, Kievit J. Adrenal incidentalomas.In: Endocrine Surgery. Schwartz AE, Pertsemlidis D, Gagner M (Eds). Marcel Dekker, NY, USA, 411–427 (2003).
  • Mansmann G, Lau J, Balk E et al. The clinically inapparent adrenal mass: update in diagnosis and management. Endocr. Rev.25, 309–340 (2004).
  • Turner H, Moore N, Byrne J, Wass J. Pituitary, adrenal and thyroid incidentalomas. Endocr. Relat. Cancer5, 131–150 (1998).
  • AACE Acromegaly Guidelines Task Force. American assocation of clinical endocrinologists medical guidelines for clinical practice for the diagnosis and treatment of acromegaly. Endocr. Pract.10, 213–225 (2004).
  • Casanueva F, Molitch M, Schlecjte J et al. Guidelines of the pituitary society for the diagnosis and management of prolactinomas. Clin. Endocrinol.65, 265–273 (2006).
  • Niemna L, Biller B, Findling J et al. The diagnosis of Cushing’s Syndrome: an endocrine society clinical practice guidelines. J. Clin. Endocrinol. Metab.93, 1526–1540 (2008).
  • Aron DC. Clinical epidemiology and evidence-based endocrinology. Basic and Clinical Endocrinology. Greenspan FS, Gardner DG (Eds). McGraw-Hill Medical, Berkshire, UK (2007).
  • Carroll T, Raff H, Findling J. Late-night salivary cortisol measurement in the diagnosis of Cushing’s syndrome. Endocrinol. Metab.4, 344–350 (2008).
  • Kidambi S, Raff H, Findling JW. Limitations of nocturnal salivary cortisol and urine free cortisol in the diagnosis of mild Cushing’s syndrome. Eur. J. Endocrinol.157, 725–731 (2007).
  • Liu H, Bravata D, Cabaccan J, Raff H, Ryzen E. Elevated late-night salivary cortisol levels in elderly male Type 2 diabetic veterans. Clin. Endocrinol.63, 642–649 (2005).
  • Gibney J, Smith T, McKenna TJ. Clinical relevance of macroprolactiemia. Clin. Endocrinol. (Oxford)62, 633–643 (2005).
  • Molitch M. Medication-induced hyperprolactinemia. Mayo Clin. Proc.80, 1050–1057 (2005).
  • Catargi B, Rigalleau V, Poussin A et al. Occult Cushing’s syndrome in Type 2 diabetes. J. Clin. Endocrinol. Metab.88, 5808–5813 (2003).
  • Newsome S, Chen K, Hoang J, Wilson JD, Potter JM, Hichman PE. Cushing’s syndrome in a clinic population with diabetes. Intern. Med. J.38, 178–182 (2008).
  • Nagai T, Imamura M, Misumi S, Mori M. Subclinical Cushing’s disease accompanied by malignant hypertension and diabetes mellitus. Intern. Med.41, 566–570 (2002).
  • Contreras L, Cardoso E, Lozano MP et al. Detection of preclinical Cushing’s syndrome in overweight Type 2 diabetic patients. Medicina (B Aires)60, 326–330 (2000)
  • Kievit J, Haak HR. Diagnosis and treatment of adrenal incidentaloma. A cost–effectiveness analysis. Endocrinol. Metab. Clin. North Am.29, 69–88 (2000).
  • Woolf SH, Kamerow DB et al. Testing for uncommon conditions. the heroic search for positive test results. Arch. Intern. Med.150, 2451–2458 (1990).
  • Mold, Stein. The cascade effect in the clinical care of patients. N. Engl. J. Med.314, 512–514 (1986).
  • Kassirer. Our stubborn quest for diagnostic certanity. A cause of excessive testing. N. Engl. J. Med.320, 1489–1491 (1989).
  • Ersoy R, Topaloglu O, Aydin C, Dirikoc A, Cakir B. Pituitary metastasis of breast cancer confirmed by fluorine-18 fluorodeoxyglucose positron emission tomography a case report. J. Endocrinol. Invest.30, 532–533 (2007).
  • Ikeda H, Abe T, Watanabe K. Usefulness of composite methionine-positron emission tomography/3.0-tesla magnetic resonance imaging to detect the localization and extent of early-stage Cushing adenoma. J. Neurosurg. DOI: 10.3171/2009.7.JNS09285 (2009) (Epub ahead of print).
  • Ryu S, Tafti B, Skirboll S. Pituitary adenomas can appear as hypermetabolic lesions in F-FDG PET imaging. J. Neuroimaging DOI: 10.1111/j.1552-6569.2008.00347.x (2009) (Epub ahead of print).
  • Alzahrani A, Farhat R, Al-Arifi A, Al-kahtani N, Kanaan I, Abouzied M. The diagnostic value of fused positron emission tomography/computed tomography in the localization of adrenocorticotropin-secreting pituitary adenoma in Cushing’s disease. Pituitary12(4), 309–314 (2009).
  • Suzuki M, Minenatsu T, Oyama K et al. Expression of proliferation markers in human pituitary incidentalomas. Endocrine Pathology17, 263–276 (2006).
  • Saeger W, Ludecke DK, Buchfelder M, Fahlbusch R, Quabbe H-J. Pathohistological classification of pituitary tumors: 10 years of experience with the German pituitary tumor registry. Eur. J. Endocrinol.156, 203–216 (2007).
  • Ferrante E, Ferrar M, Tristana C et al. Non-functioning pituitary adenoma data: a useful resource to improve the clinical management of pituitary tumors. Eur. J. Endocrinol.155, 823–829 (2006).
  • Drange MR, Fram NR, Herman-Bonert V, Melmed S. Pituitary tumor registry: a novel clinical resource. J. Clin. Endocrinol. Metab.85, 168–174 (2000).
  • Ramsey R. Evaluation of incidental findings on MRI of the central nervous system: part II. J. Insur. Med. (Seattle)37, 158–165 (2005).
  • Ramsey R. Evaluation of incidental findings on MRI of the central nervous system: part I. J. Insur. Med. (Seattle)36, 167–173 (2002).
  • Illes J, Kirschen M, Edwards E et al. Incidental findings in brain imaging research. Science311, 783–784 (2006).
  • Stone JH. Incidentalomas – clinical correlation and transslational science required. N. Engl. J. Med.354, 2748–2749 (2006).

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