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Adrenal incidentaloma

In medicine, an incidentaloma is a tumor (-oma) found by coincidence (incidental) without clinical symptoms and suspicion. It is a common problem: up to 7% of all patients over 60 may harbor a benign growth, often of the adrenal gland, which is detected when diagnostic imaging is used for the analysis of unrelated symptoms. With the increase of "whole-body CT scanning" as part of health screening programs, the chance of finding incidentalomas is expected to increase. more...

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When faced with an unexpected finding on diagnostic imaging, the clinician faces the challenge to prove that the lesion is indeed harmless. Often, some other tests are required to determine the exact nature of an incidentaloma.

Adrenal incidentaloma

In adrenal gland tumors, a dexamethasone suppression test is often used to detect cortisol excess, and metanephrines or catecholamines for excess of these hormones. Tumors under 3 cm are generally considered benign and are only treated if there are grounds for a diagnosis of Cushing's syndrome or pheochromocytoma (Grumbach et al 2003).

Pituitary incidentaloma

Autospy series have suggested that pituitary incidentalomas may be quite common. It has been estimated that perhaps 10% of the adult population may harbor such endocrinologically inert lesions (Hall et al). When encountering such a lesion, long term surveillance has been recommended (Molitch). Also baseline pituitary hormonal function needs to be checked, inculding measurements of serum levels of TSH, prolactin, IGF-I (as a test of growth hormone activity), and adrenal function (i.e. dexamethasone suppression test).

Others

Other organs that can harbor incidentalomas are the liver (often a hemangioma), thyroid, parathyroid, and the kidneys.

Scientific criticism

The concept of the incidentaloma has been criticized, as such lesions do not have much in common other than the history of an incidental identification and the assumption that they are clinically inert. It has been proposed just to say that such lesions have been "incidentally found." (Miralas et al) The underlying pathology shows no unifying histological concept.

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Hypophysial insufficiency in old age: a forgotten syndrome?
From Age and Ageing, 3/1/98 by Fernando Jose Ruiz Laiglesia

SIR--Non-functional pituitary adenoma is the most common cause of pan-hypopituitarism, but it is not often diagnosed in old age. Perhaps many adenomas do not cause hypophysial hypofunction, or their manifestations, if they arise, may be underestimated. We describe two older patients with chronic general malaise which was initially attributed to depression and which was found to be caused by hypophysial insufficiency resulting from a non-functioning adenoma. Both cases were characterized both by delay in diagnosis and treatment and by a gratifying response to hormone replacement.

Hypopituitarism is uncommon in elderly people and is rarely mentioned in standard texts of geriatric medicine [1]. Its clinical presentations may be non-specific and there are physiological endocrinological changes associated with age which may confound the interpretation of analytical data. This may lead to a delay in diagnosis and treatment.

Case 1: a 76-year-old man presented with a long history of fatigue, anorexia, drowsiness and slowed intellectual and motor activity. This combination of symptoms had been treated as a depressive syndrome but no improvement had taken place. Eventually, after an acute behavioural disturbance, the patient was admitted. The hormonal study showed hypopituitarism (Table 1). The plain skull radiographs revealed an enlarged pituitary fossa with erosion of posterior clinoid caused by a non-functional hypophysial adenoma of 28 mm diameter. We instituted a conservative treatment with 30 mg hydrocortisone and 253 [micro]g levothyroxine per 24 h, increasing the levothyroxine to 150 [micro]g per 24 h. The clinical response to hormone therapy was spectacular.

HGH, human growth hormone; TSH, thyroid stimulating hormone; ACTH, adrenocorticotrophic hormone; PRL, prolactin; LH, leutinizing hormone; FSH, follicle stimulating hormone; T3, triiodothyronine; T4, thyroxine.

Case 2: a 72-year-old man with a depressive syndrome for over 2 years was admitted with a decrease in the level of consciousness. No motor deficiency was observed, but there was left homonymous hemianopia. On computerized axial tomography, multiple non-acute ischaemic infarcts were observed, together with a hypophysial adenoma with infra- and suprasellar growth which was destroying the posterior clinoid. After intravenous therapy his general condition improved and he was discharged pending the results of tine functional studies. No hormonal treatment was prescribed. He was readmitted 30 days later to the internal medicine department due to a further drop in level of consciousness. The results of the functional studies (Table 1) confirmed hypopituitarism. Replacement treatment was initiated with hydro-cortisone and levothyroxine with a good response. Following initiation of therapy a spontaneous decrease in tumour size was observed.

Non-functioning pituitary adenoma is the most common cause of hypophysial insufficiency in the elderly patient [2, 4]. In one autopsy series, pituitary adenomas were found in 10-20% of autopsies of subjects not suspected of having pituitary disease, although only 0.28% were greater than 10 mm in diameter [5]. This suggests that many adenomas do not cause hypophysial hypofunction, or that any manifestations that do arise are overlooked in subjects of over 65. In younger subjects, symptoms of thyroid, adrenal or gonadal insufficiency or visual field defects are usual [61, while in elderly subjects malaise, confusion or falls predominate and may be.' attributed to other diseases [2, 7].

In the assessment of hormonal assays, one must consider the somatic and biological changes that may accompany old age and illness, and drugs that may interfere with the interpretation [8, 9].

To detect hypophysial insufficiency, some authors consider it essential to determine the serum sodium and thyroxine concentrations [7], while others only consider it necessary to measure the thyroid stimulating hormone [1]. The insulin-induced hypoglycaemia test is not recommended for elderly patients with cardiac diseases.

Although trans-sphenoidal hypophysectomy is recommended when there are visual deficiencies or evidence of tumour growth [5, 6], our second patient had a spontaneous reduction in tumour size (as did three of the 12 macro-adenomas in another series [10]). In both cases, hormone replacement treatment was followed by a dramatic improvement in symptoms and quality of life.

Fernando Jose Ruiz Laiglesia Fermin Reclusa Poyo Carmen Torrubia Perez Department of Internal Medicine, Hospital Clinico Universitario `Lozano Blesa' Zaragoza, Spain (Address correspondence to F. J. Ruiz Laiglesia, C/Duquesa Villahermosa 159, 1 [degrees] B, Zaragoza 50009, Spain)

[1.] Hall MRP. The endocrine system. The hypophyso-adrenal axis. In: Brocklehurst JC ed. Textbook of Geriatric Medicine and Gerontology. Edinburgh: Churchill Livingstone, 1985.

[2.] Tayal SC, Bansal SK, Chadha DK. Hypopituitarism: a difficult diagnosis in elderly people but worth a search. Age Ageing 1994; 23: 148-53.

[3.] Antunes JL, Housepain EM, Frantz AG et al. Prolactin-secreting pituitary tumours. Ann Neurol 1978; 2: 148-53.

[4.] Godfrey JB, Caird FI. Intracranial tumours in the elderly: diagnosis and treatment. Age Ageing 1984; 13: 152-8.

[5.] Molitch ME, Russel EJ. The pituitary `incidentaloma'. Ann Intern Med 1990; 112: 925-31.

[6.] Cohen DL, Bevan JS, Adams BT. The presentation and management of pituitary tumours in the elderly. Age Ageing 1989; 18: 247-52.

[7.] MacLennan WJ, Peden NR. Pituitary tumours. In: Metabolic and Endocrine Problems in the Elderly. London: Springer-Verlag, 1989.

[8.] Harvard CWH. The thyroid and ageing. Clin Endocrinol Metab 1981; 10: 163-78.

[9.] Rae P, Farrer J, Beckett G et al. Assessment of thyroid status in elderly people. Br Med J 1993; 307:177-80.

[10.] Reinck M, Deub U, Jaursch-Hancke C, Winkelmann W. The incidentally discovered pituitary mass--is neurosurgery required? (Abstract). Program and Abstracts of the 71st Annual Meeting of the Endocrine Society, Seattle, WA, 1989; A179

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COPYRIGHT 2000 Gale Group

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