Differential diagnosis, investigation and therapy of bilateral adrenal incidentalomas

被引:51
作者
Bourdeau, Isabelle [1 ]
El Ghorayeb, Nada [1 ]
Gagnon, Nadia [1 ]
Lacroix, Andra [1 ]
机构
[1] Univ Montreal, CRCHUM, Div Endocrinol, Dept Med, Montreal, PQ, Canada
关键词
SUBCLINICAL CUSHINGS-SYNDROME; OF-THE-LITERATURE; MACRONODULAR ADRENOCORTICAL HYPERPLASIA; CLINICAL-PRACTICE GUIDELINE; 21-HYDROXYLASE DEFICIENCY; ARMC5; MUTATIONS; UNILATERAL ADRENALECTOMY; IMAGING CHARACTERIZATION; CORTISOL HYPERSECRETION; HORMONE-RECEPTORS;
D O I
10.1530/EJE-18-0296
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The investigation and management of unilateral adrenal incidentalomas have been extensively considered in the last decades. While bilateral adrenal incidentalomas represent about 15% of adrenal incidentalomas (Als), they have been less frequently discussed. The differential diagnosis of bilateral incidentalomas includes metastasis, primary bilateral macronodular adrenal hyperplasia and bilateral cortical adenomas. Less frequent etiologies are bilateral pheochromocytomas, congenital adrenal hyperplasia (CAH), Cushing's disease or ectopic ACTH secretion with secondary bilateral adrenal hyperplasia, primary malignancies, myelolipomas, infections or hemorrhage. The investigation of bilateral incidentalomas includes the same hormonal evaluation to exclude excess hormone secretion as recommended in unilateral Al, but diagnosis of CAH and adrenal insufficiency should also be excluded. This review is focused on the differential diagnosis, investigation and treatment of bilateral Als.
引用
收藏
页码:R57 / R67
页数:11
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