2017
DOI: 10.1515/rjim-2017-0025
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A step by step approach in differential diagnosing of adrenal incidentaloma (epinephroma), (with comments on the new Clinical Practice Guidelines of the European Society of Endocrinology)

Abstract: Density less than 10 HU is in most cases characteristic of a lipid rich benign adenoma. More than 10 HU or/and history of malignancy raise the possibility for cancer. 1 mg dexamethasone test and plasma metanephrines should be done in all patients. If there is history of hypokalemia and/or resistant hypertension we test the plasma aldosterone to plasma renin ratio (ARR). Newer studies have shown that tumours even nonfunctioning and less than 4 cm may increase the metabolic risks so we may consider surgery at an… Show more

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Cited by 2 publications
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“…We recommend referring patients to an endocrinology clinician if the patient is a child or has: • a lesion 4 cm or greater • specific concerning findings on imaging such as inhomogeneity, irregular borders, or calcifications • a lesion that increases in size over time TABLE 4. Management and referral considerations for adrenal masses 1,5,18,20,24,29,30,32,33 Nonfunctioning adrenal adenoma smaller than 4 cm • bilateral adrenal masses • an abnormal screening hormonal evaluation • overt features of adrenal hormone excess on physical examination • a personal history of malignancy • a family history of endocrine tumors and/or genetic syndromes that are associated with adrenal masses. A discussion of management and referral recommendations is detailed in Table 4.…”
Section: Management and Referralmentioning
confidence: 99%
“…We recommend referring patients to an endocrinology clinician if the patient is a child or has: • a lesion 4 cm or greater • specific concerning findings on imaging such as inhomogeneity, irregular borders, or calcifications • a lesion that increases in size over time TABLE 4. Management and referral considerations for adrenal masses 1,5,18,20,24,29,30,32,33 Nonfunctioning adrenal adenoma smaller than 4 cm • bilateral adrenal masses • an abnormal screening hormonal evaluation • overt features of adrenal hormone excess on physical examination • a personal history of malignancy • a family history of endocrine tumors and/or genetic syndromes that are associated with adrenal masses. A discussion of management and referral recommendations is detailed in Table 4.…”
Section: Management and Referralmentioning
confidence: 99%