Cancer, Adrenal Metastasis


Article Author:
Shashank Cingam


Article Editor:
Harsha Karanchi


Editors In Chief:
Susan Johnson
Alexandra Caley


Managing Editors:
Avais Raja
Orawan Chaigasame
Carrie Smith
Abdul Waheed
Khalid Alsayouri
Frank Smeeks
Kristina Soman-Faulkner
Radia Jamil
Patrick Le
Sobhan Daneshfar
Anoosh Zafar Gondal
Saad Nazir
William Gossman
Pritesh Sheth
Hassam Zulfiqar
Navid Mahabadi
Steve Bhimji
John Shell
Matthew Varacallo
Heba Mahdy
Ahmad Malik
Mark Pellegrini
James Hughes
Beata Beatty
Nazia Sadiq
Hajira Basit
Phillip Hynes
Tehmina Warsi


Updated:
1/20/2019 8:34:12 AM

Introduction

Adrenal metastases are the most common malignant lesions involving the adrenal gland and the second most common tumor of the adrenal gland after benign adenomas. These metastases were primarily found on autopsy. However, with the increasing role of CT, MRI, and PET in diagnosing, staging, and follow-up of malignancies, adrenal metastases are increasingly found incidentally.[1][2][3]

Etiology

Adrenal glands are the fourth most common site of metastases in malignant disease, which is significant considering the relatively small size of adrenals. Adrenal metastasis can occur from primaries in the lung (39%), breast (35%), melanoma, gastrointestinal tract, pancreas, and kidney among other places.[4][5][6]

Epidemiology

About 30% to 70% of incidentally discovered adrenal masses in patients with a history of cancer or a recently diagnosed extra-adrenal malignancy are metastases. The incidence of these metastases might be higher in autopsies. For example, in a study, the incidence of adrenal metastases from renal cell carcinoma was 6% to 29% in autopsy series, but from clinical diagnosis, it was less frequent, at 2% to 10%. The median time from cancer diagnosis to the identification of adrenal metastases is about 2.5 years, although adrenal metastases have been reported up to 22 years after initial treatment of primary tumors. It is uncommon for isolated adrenal metastases to occur before identification of the primary malignancy. The increasing incidence of breast and lung cancer, as well as other types of cancer, has also resulted in an increase of adrenal metastases.

Pathophysiology

Metastatic spread to the adrenals is mainly hematogenous and can be bilateral. Lymphogenous spread to the adrenals is widely debated. It is poorly understood why metastases have a predilection to adrenals, although it is hypothesized that it is due to its rich sinusoidal blood supply. On gross pathology, metastases are gray-white, tan-brown, or black colored, solitary or multiple, firm heterogeneous masses, with occasional hemorrhage and necrosis. On cytology, metastatic lesions are morphologically similar to the primary tumor. The tumor cells exhibit increased nuclear hyperchromasia, prominent nucleoli, frequent mitotic figures, necrotic debris, and intact cells with increased nuclear and cytoplasmic ratios as against adrenal adenomas which are composed of relatively uniform cells without mitosis or necrosis. Immunohistochemical markers could be helpful to separate metastatic tumors from primary, adrenocortical tumors.[7][8][9]

History and Physical

Most patients with adrenal metastases are asymptomatic. Patients may have localized symptoms like back or abdominal pain due to tumor mass effect if the tumor is large or rapidly growing. This could indicate local invasion or retroperitoneal hemorrhage.

Adrenal metastases do not usually result in adrenal insufficiency unless a significant portion of the bilateral adrenals ( more than 90%) are affected. These patients can present with anorexia, weight loss, nausea, vomiting, abdominal pain, weakness, fatigue, lethargy, fever, confusion, electrolyte imbalances secondary to adrenal insufficiency, and can be easily confused with the manifestations of the neoplastic disease. Adrenal crisis due to episodes of symptomatic hemorrhage into adrenal glands which were infiltrated by a metastatic tumor has rarely been noted. 

Evaluation

The presence of metastases influences the management of the primary malignancy, and further evaluation is often needed, especially in patients with cancer with no other sites of metastases besides the adrenal glands.

Imaging

Most adrenal tumors are benign, and many are indeterminate on imaging. Based on current studies, no single imaging modality can be considered the gold standard for the comprehensive evaluation of adrenal incidentalomas or to distinguish malignant from benign adrenal masses. CT and MRI assess lipid content to differentiate benign (high lipid content) from potentially malignant (low lipid content) adrenal masses and are mainly used to identify benign lesions and exclude adrenal malignancy. FDG-PET/CT is mainly used for detection of malignant disease. The pre-test probability of an indeterminate adrenal mass being malignant is greater in a patient with a history of extra-adrenal malignancy but requires careful exclusion of other causes. Any available previous imaging is extremely useful for comparison and also for determining the timeline of onset and growth.

On CT, adrenal metastases typically have a higher unenhanced density (greater than 10 HU), are heterogeneous, and have a delay in contrast medium washout compared to adenomas (pre-contrast HU less than 10, homogeneous, and rapid contrast washout). Assessment of precontrast density by itself is not as specific because a third of the benign adrenal adenomas are lipid-poor and have HU greater than 10, thereby necessitating CT with contrast enhancement for washout characteristics if the adrenal mass has attenuation higher than 10 HU on non-contrast CT. Although precontrast HU less than 10 is unlikely to be malignant, we have to be cautious about a pooled false negative rate of 7% in patients with a history of extra-adrenal malignancy. Measurement of HU needs to be standardized to be accurate. The region of interest during measurement of attenuation should encompass two-thirds of the largest axial diameter of the mass and avoid boundaries. It is inaccurate if areas of necrosis are present. Lesions greater than four centimeters have a higher risk of malignancy. The growth of an adrenal lesion over short-term imaging follow-up (i.e., six months), local invasion, irregular borders, and central necrosis are predictors of primary adrenal malignancy and adrenal metastasis. Calcification is rare in adrenal metastases.

MRI has a limited role in characterizing lipid-poor adrenal masses especially when pre-contrast HU>20-30 and thus adrenal metastases. On MRI, adrenal metastases are isointense or slightly hypointense on T1 weighted images and hyperintense on T2 weighted images with heterogeneous enhancement after administration of contrast. On chemical-shift MRI, metastases typically do not show signal drop during out-of-phase sequences due to the poor lipid nature of the adrenal metastasis. Rarely, metastases secondary to clear renal cell carcinoma and hepatocellular carcinoma can mimic adenoma on chemical shift MRI due to intracytoplasmic lipid.

An 18F-fluorodeoxyglucose PET (18F-FDG PET), although not a specific marker for cancer cells, has 74% to 100% sensitivity and 66% to 100% specificity in differentiating adrenal masses as benign or malignant in patients with known primary cancers. The degree of hypermetabolism on a PET is measured by standardized uptake value. Mean adrenal standardized uptake value max, and adrenal-to-liver standardized uptake value ratio is higher for adrenal metastases than for adenomas. An adrenal max standardized uptake value cutoff of 3.1, has been shown to have a sensitivity of 98.5% and specificity of 92% for differentiating benign adenomas from malignant lesions. An SUV adrenal lesion/liver ratio greater than 1.8 with a history of extra-adrenal malignancy has a sensitivity of 82% and specificity of 96% to detect malignant disease. PET-CT is subject to both false positive (some benign adrenal adenomas, inflammatory lesions such as sarcoidosis and tuberculosis) and false negative results (less than 1 cm metastatic nodules, metastases with hemorrhage or necrosis, metastases from non-FDG avid malignancies) and cannot differentiate adrenal metastases from adrenocortical carcinoma.

Biopsy

CT-guided fine-needle aspiration (FNA) may be useful when imaging is equivocal (has not been conclusively characterized as benign), the lesion is hormonally inactive, and most importantly, the management of the patient would be altered with information from histology. Therefore, FNA is not useful in the setting of widespread metastatic disease but may have utility in the setting of evaluation for the oligometastatic disease to the adrenal gland. It is of utmost importance that pheochromocytoma is excluded with biochemical testing (plasma or urinary metanephrines) before the biopsy to avoid the potential risk of hypertensive crisis and life-threatening complications. FNA should not be done if the mass is likely to be adrenocortical carcinoma because this rarely provides an answer and also because of the risk of dissemination precluding R0 resection. Although FNA cannot differentiate between benign adenoma and adrenocortical carcinoma, FNA is very useful in confirming the presence of metastatic disease in adrenal lesions with a sensitivity of 80% to 90% and positive predictive value of 100%. FNA has the potential for non-diagnostic results (0% to 28%) and complications (2.5% to 13%) Most complications are self-limiting but can include adrenal hemorrhage, pain, pancreatitis, pneumothorax, and hematuria.

Biochemical Evaluation

With CT, MRI, and PET scans it is not possible to reliably distinguish pheochromocytoma from metastases. Therefore, it is important to rule out pheochromocytoma in patients with extra-adrenal malignancy with an indeterminate mass, even if the adrenal mass is likely to be metastatic. Additional hormonal work up for hyperfunctioning (Cushing syndrome, primary hyperaldosteronism) should be individualized, and patients with advanced stage and limited life expectancy are unlikely to benefit. As bilateral adrenal metastases can lead to adrenal insufficiency in rare cases, all patients with potentially bilateral metastases should be clinically evaluated for adrenal insufficiency. The initial test is morning adrenocorticotropic hormone (ACTH) and cortisol in addition to serum electrolytes, and if the diagnosis is not cleared by the patient's history and initial testing, an ACTH stimulation test should be done. In the setting of unilateral adrenal metastases, adrenal insufficiency is unlikely and typically does not need evaluation. In patients with a history of cancer and use of glucocorticoids as part of chemotherapy regimen or otherwise over the last year, the possibility of glucocorticoid-related adrenal suppression should be considered. In this scenario, stress dose glucocorticoids during admission for critical illness, surgery or procedures requiring conscious sedation or anesthesia should be strongly considered to prevent adrenal crisis.

Treatment / Management

The most effective treatment of adrenal metastases is first to treat the primary cancer, usually with chemotherapy and/or radiation therapy. Surgical resection is considered in patients with isolated adrenal metastasic disease or with other resectable or potentially curable metastases. A PET scan is useful for the detection of oligometastatic disease to the adrenals and excludes extra-adrenal metastatic disease if not already evident by CT or MRI. An absence of local invasion into contiguous structures and a disease-free interval greater than six months from the original cancer diagnosis are considered good prognostic factors with adrenalectomy. Results vary depending on the cancer site of origin. There is no evidence supporting an adrenalectomy for tumors with an unknown primary source. Minimally invasive laparoscopic adrenalectomy is as effective as open adrenalectomy for adrenal metastasectomy with proven reduction in postoperative pain, morbidity, and length of stay. Adrenal masses less than 6 cm without local invasion are amenable to laparoscopic adrenalectomy. Radiotherapy, radiofrequency ablation, arterial ablation, chemoablation, cryoablation, and CT-guided or MR thermotherapy-controlled laser- induced, interstitial thermotherapy have been used with curative and palliative intent and have shown variable results. Imaging-guided thermal ablation of adrenal metastases with radiofrequency ablation, cryoablation, and microwave ablation has the potential for local tumor control but risks include hemodynamic complications (hypertensive urgency) and adrenal insufficiency. Pre-ablation alpha blockade has been shown to reduce the severity of the hypertensive episodes but increases need for vasopressors periprocedural. It is important to assess adrenal function after ablation and provide glucocorticoid replacement as needed.

Enhancing Healthcare Team Outcomes

Adrenal metastases are the most common malignant lesions involving the adrenal gland and the second most common tumor of the adrenal gland after benign adenomas. These metastases were primarily found on autopsy. However, with the increasing role of CT, MRI, and PET in diagnosing, staging, and follow-up of malignancies, adrenal metastases are increasingly found incidentally. The management of adrenal metastatic lesions is best done with a multidisciplinary team that includes an oncologist, a surgeon, radiologist, primary care provider, internist, and a pathologist. The key is to find out the primary. In most cases the biggest difficulty is determining if the adrenal lesion is benign or a metastatic lesion. Sometimes a biopsy or laparoscopy may be required. If the lesion is metastatic the prognosis for most patients is poor. 


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Cancer, Adrenal Metastasis - Questions

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A 63-year-old, male smoker presents with hemoptysis and weight loss. A CT revealed a 4 x 4 cm central lung mass, with irregular margins and central cavitation which was later diagnosed by biopsy as a squamous cell carcinoma of the lung. CT also revealed 4 cm and 2 cm heterogeneous left and right adrenal masses respectively with high density (14 HU). PET showed metabolically active lung and adrenal mass with a max SUV of 2.2 without any other evidence of metastatic spread.What is the next step of management?



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A non-specific adrenal mass is found on CT in a patient with no known primary malignancy. The ordering physician asks if she should be concerned about it representing a metastasis from an unknown primary. What is the correct response?



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Cancer, Adrenal Metastasis - References

References

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Blažeković I,Jukić T,Granić R,Punda M,Franceschi M, An Unusual Case of Papillary Thyroid Carcinoma Iodine-131 Avid Metastasis to the Adrenal Gland. Acta clinica Croatica. 2018 Jun;     [PubMed]
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