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adrenal cortical adenoma

Pathology: - adrenal adenomas are generally < 4 cm [1] - most associated with Cushing's syndrome are unilateral - most hyperaldosteronism associated are unilateral & solitary - androgen-secreting neoplasm - nonfunctioning adenomas or nodules seen with increasing age Genetics: - occasionally associated with mutations in APC gene - other implicated genes GADD45GIP1 Clinical manifestations: - may be associated with - overproduction of glucocorticoids (Cushing's syndrome) - overproduction of androgenic/estrogenic steroids (adrenogenital syndrome) - overproduction of mineralocorticoids (Conn's syndrome) - adrenal adenomas can exhibit both Cushing's syndrome & hyperandrogenism but this is uncommon [3] Laboratory: - see adrenal incidentaloma Radiology: - contrast-enhanced abdominal computed tomography - generally < 4 cm with round with clear margins* - homogenous enhancement* - density < 10 HU* - contrast washout > 50% in 10 minutes [1]* - magnetic resonance imaging (MRI) - isointense on T2 weighted images [1]* * compare with adrenal cortical carcinoma Differential diagnosis: - adrenal cortical hyperplasia - adrenal cortical carcinoma (distinguishing CT characteristics) Management: - see adrenal incidentaloma

Related

adrenal cortical carcinoma

Specific

adrenal incidentaloma

General

adenoma adrenal neoplasm

References

  1. Medical Knowledge Self Assessment Program (MKSAP) 17, 18. American College of Physicians, Philadelphia 2015, 2018.
  2. Cordera F, Grant C, van Heerden J, Thompson G, Young W. Androgen-secreting adrenal tumors. Surgery. 2003 Dec;134(6):874-80; discussion 880. PMID: 14668717
  3. Tanaka S, Tanabe A, Aiba M, et al. Glucocorticoid- And Androgen-Secreting Black Adrenocortical Adenomas: Unique Cause of Corticotropin-Independent Cushing Syndrome. Endocrine Practice. 2011 May-Jun;17(3):e73-8 PMID: 21700558

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