Evaluation of Adrenal Incidentaloma

被引:2
作者
Hu, Jiangnan [1 ]
Kassu, Rodas [1 ]
Titanji, Bosung [2 ]
Kebebew, Electron [3 ]
机构
[1] Stanford Univ, Sch Med, Dept Surg, Div Gen Surg, 269 Campus Dr,CCSR-3100, Stanford, CA 94305 USA
[2] Meharry Med Coll, 1005 Dr DB Todd Jr Blvd, Nashville, TN 37208 USA
[3] Stanford Univ, Sch Med, Dept Surg, Div Gen Surg, 300 Pasteur Dr,H3642, Stanford, CA 94305 USA
关键词
Adrenal incidentaloma; Hormonal workup; Pheochromocytoma; Primary hyperaldosteronism; Cushing's syndrome; Adrenal malignancy; Adrenalectomy; AUTONOMOUS CORTISOL SECRETION; C-11-METOMIDATE PET-CT; PRIMARY ALDOSTERONISM; CARDIOVASCULAR EVENTS; INCREASED MORTALITY; EUROPEAN-SOCIETY; MANAGEMENT; PHEOCHROMOCYTOMA; HYPERCORTISOLISM; COLLABORATION;
D O I
10.1016/j.suc.2024.02.012
中图分类号
R61 [外科手术学];
学科分类号
摘要
Adrenal incidentalomas require a comprehensive history and physical examination, with a focus on identifying evidence of excess adrenal hormonal secretion. Biochemical testing is needed to exclude mild autonomous cortisol excess, a pheochromocytoma, and/or primary hyperaldosteronism (in patients with hypertension and or hypokalemia). A patient with inconclusive biochemical testing should undergo confirmatory testing (mild autonomous cortisol excess and primary hyperaldosteronism). All patients with a pheochromocytoma should be offered an adrenalectomy (minimally invasive if there is no suspicion of a malignant tumor). Patients with mild autonomous cortisol excess and associated metabolic complications should also be offered an adrenalectomy because most patients have reversal of the metabolic complications and reduced long-term risk of cardiovascular disease. Patients who have primary hyperaldosteronism benefit from an adrenalectomy if they have unilateral hypersecretion. If the patient has a nonfunctional tumor less than 4 cm with indeterminate imaging features, then clinical follow-up is recommended.
引用
收藏
页码:837 / 849
页数:13
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