Myelolipomatous Adrenal Adenoma and Adrenal Scintigraphy: A Case Presentation and Review of Literature
Abstract
Adrenal myelolipomas are usually benign and non-functioning masses. On  the other hand, adrenal myelolipomatous adenoma that may mimic adrenal  myelolipoma on conventional imaging may be a rare cause of subclinical  Cushing’s disease. Adrenal scintigraphy (with 131I-6beta-iodomethyl-19-norcholesterol)  can be used to demonstrate increased uptake in a functioning adrenal  myelolipomatous adenoma to distinguish it from an adrenal myelolipoma,  when the source of the excess hormone secretion after biochemical  evaluation is unclear. Treating physicians should be familiar with the  occasional use of this imaging modality that can help distinguish  functional adrenal tumors from non-functioning ones when conventional  imaging fails to do so. A 66-year-old female was found to have an  incidental 6.5 cm right adrenal mass during a routine abdominal  ultrasound. Complete biochemical evaluation was suggestive of  subclinical Cushing’s syndrome. Imaging studies were consistent with  adrenal myelolipoma. Adrenal scintigraphy showed a unilateral increased  uptake at the site of the adrenal mass. She successfully underwent  laparoscopic adrenalectomy of the 6.5 cm mass and she had significant  clinical improvement. Myelolipomatous adrenal adenoma (that may mimic  adrenal myelolipoma on conventional imaging) may be a rare cause of  subclinical Cushing’s, and adrenal scintigraphy may be a useful imaging  technique that may help in localizing the lesion, which can then be  treated surgically.
J Endocrinol Metab. 2014;4(5-6):148-150
doi: http://dx.doi.org/10.14740/jem254w
		J Endocrinol Metab. 2014;4(5-6):148-150
doi: http://dx.doi.org/10.14740/jem254w
Keywords
Adrenal cortex neoplasms; 19-Iodocholesterol; Myelolipoma
		