Adrenal adenoma

Last revised by Henry Knipe on 11 Jul 2024

Adrenal adenomas (alternative plural: adenomata) are the most common adrenal lesion and are often found incidentally during abdominal imaging for other reasons. In all cases, but especially in the setting of known current or previous malignancy, adrenal adenomas need to be distinguished from adrenal metastases or other adrenal malignancies.

The term incidental adrenal lesion/nodule (also colloquially known as an incidentaloma) is sometimes used interchangeably with adrenal adenoma, although in truth an incidental adrenal lesion includes all pathologies (including malignancies). As such, the term should be avoided lest it results in confusion.

Adrenal adenomas are found in almost all age groups but increase in frequency with age 4.

The majority (~95%) of adrenal adenomas are non-functioning, in which case they are asymptomatic. If found incidentally, please refer to the Management of incidental adrenal masses: American College of Radiology white paper.

Patients with hyperfunctioning adrenal gland adenomas present with manifestations of excess hormone secretion. The most common disease states caused by functioning adenomas are Cushing syndrome (due to excess cortisol production), Conn syndrome (due to excess aldosterone production), or sex hormone-related symptoms 4.

Imaging plays a key role in assessing the vast number of incidental adrenal lesions, the majority of which are adrenal adenomas. Correlation with previous imaging is often useful, as a lesion which has not changed over some years is unlikely to be malignant.

Adrenal adenomas can be divided into those with a typical or an atypical appearance.

Typical adenomas are:

  • small: <3 cm

  • round, or ovoid homogeneous with low density and smooth borders 20 

Atypical features include:

  • hemorrhage

  • calcification

  • necrosis

  • lack or paucity of fat

  • macroscopic fat: rare; seen in lipomatous metaplasia 22

  • large

    • if >4 cm: 70% malignant (excluding adrenal myelolipomas which are easily recognized due to fat, and pheochromocytomas which are usually recognized biochemically)

    • if >6 cm: 85% malignant 4

CT is often the modality which identifies an adrenal mass. Fortunately, density evaluation of an adrenal lesion is highly sensitive and specific as 70% of adrenal adenomas contain significant intracellular fat. Lipid-poor adenomas are more difficult to diagnose as the CT density increases and approach that of soft tissue.

For lipid-poor lesions, the contrast washout rate can be calculated using CT adrenals. Adenomas typically have rapid contrast washout, whereas non-adenomas tend to wash out more slowly. There are different protocols, and some controversy exists as to which protocol is the best. A 5 or 10-minute protocol may be more suitable for busy CT lists. However, there is evidence that a 15 minutes post-contrast protocol has better diagnostic accuracy 11.

  • non-contrast imaging 4

    • <0 HU: considered 47% sensitive and 100% specific

    • <10 HU: considered 71% sensitive and 98% specific

  • washout imaging

    • 15 minutes post-contrast

    • >60% absolute washout

    • >40% relative washout

It is important to note that pheochromocytomas and hypervascular metastases may show identical washout values, particularly those from renal cell carcinoma and hepatocellular carcinoma 16,18.

Chemical shift imaging is the most reliable for diagnosis especially when CT findings are equivocal. Because of the high sensitivity of chemical shift, MR imaging to minute amounts of intravoxel (i.e. intracellular) fat, MR imaging demonstrates signal dropout on opposed-phase images in the majority of adenomas, and a drop in signal intensity of >16.5% is considered diagnostic for an adenoma 17,18. Rather than measuring the signal, one can compare the adenoma in and out of phase, with images windowed identically, a visible loss of signal is diagnostic of an adenoma 17,18. Do not use the liver as a reference, as it can change in signal between in- and out-of-phase imaging, depending on the presence of hemochromatosis or hepatic steatosis 4.

As MRIs are usually performed to help define indeterminate adrenal lesions seen on CT, the sensitivity and specificity depend on the CT density. MRI is useful for adrenal masses with an attenuation <30 HU 18. Signal dropout on out-of-phase imaging for:

  • 10-30 HU on CT is 89% sensitive and 100% specific

  • 10-20 HU on CT is 100% sensitive and 100% specific

Fat-containing metastases (e.g. hepatocellular carcinoma, renal cell carcinoma) can demonstrate loss of signal similar to adenomas 17,18. Malignant adrenal lesions also demonstrate restricted diffusion 4.

Small adrenal masses with manifestations of hormonal excess require resection, as do large (>3-5 cm) non-functioning adrenal mass lesions, as they are considered potentially malignant (see adrenal carcinoma).

A small adrenal lesion with typical features of an adenoma and without biochemical abnormality can be safely left in situ. Some studies demonstrate that up to 40% of adenomas may grow and approximately 10% have been shown to resolve 14.

One article proposes that if the adrenal adenoma shows expansion of more than 1 cm per annum or shows high hormonal levels, then adrenalectomy is recommended 21.

In patients with a known malignancy, ~50% of non-specific adrenal nodules will represent adrenal adenomas.

Consider other adrenal lesions such as:

  • attenuation measurements should have an ROI covering two-thirds of the lesion and excluding calcifications and the periphery of the lesion to avoid volume averaging 18

  • small (<3 cm), homogeneous, and low density (<10 HU) adenomas are "leave alone" lesions

  • lesions with attenuation values >20-30HU on non-contrast CT are unlikely to be shown as adenomas on chemical shift MRI and may rather benefit from a dynamic contrast CT study 16

  • if >120 HU on the portal venous phase, the washout value should be ignored, as the lesion is most likely a hypervascular metastasis or pheochromocytoma rather than a lipid-poor adenoma 12

  • be aware that HCC and RCC may contain intracellular fat and, therefore, their metastasis may mimic adenoma 12

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