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Adrenal Cancer Early Detection, Diagnosis, and Staging
Learn about the signs and symptoms of adrenal cancer, how it is diagnosed and staged, and what to expect after a diagnosis.
For information on neuroblastoma, a cancer that often begins in the inner part of adrenal glands, see Early Detection, Diagnosis and Staging of Neuroblastoma.
Can adrenal cancer be found early?
Adrenal cancers in adults can often grow without causing symptoms for some time. Because of this, tumors can be quite large by the time they are diagnosed. In adults, adrenal tumors can be found before symptoms when imaging tests are done for some other reason. These tumors are often not cancers, but more testing is needed to know for sure.
In children, adrenal cancers such as adrenocortical carcinoma, are more likely to make hormones. These can cause early signs of puberty which might lead to an earlier diagnosis.
Screening tests for adrenal cancer
Because adrenal cancers are rare, no screening tests are recommended for people at average risk of adrenal cancer.
People with certain family cancer syndromes have a higher risk of adrenal tumors, including adrenal cancers in some cases. People with a family cancer syndrome may have cancer screening recommendations that include adrenal cancer.
If you have a family cancer syndrome, talk to your doctor about whether adrenal cancer screening is recommended for you.
What are the signs and symptoms of adrenal cancer?
Adrenal cancers can cause symptoms because of their size or hormones they make. The symptoms of adrenal cancer depend on which extra hormones are made by the tumor. For example, in young children, adrenocortical carcinoma can make sex hormones, causing early puberty changes such as pubic hair growth. Other hormones cause other signs and symptoms.
About 1 in 5 adrenal cancers are found before any signs or symptoms. They’re usually found during an imaging test done for another reason.
How is adrenal cancer diagnosed?
Adrenal cancer is often first suspected when imaging tests show a tumor on the adrenal gland. Your healthcare team then uses other tests to learn more about the tumor and determine if it is cancerous. This might include other imaging tests, blood or urine tests, or surgery to remove all or part of the adrenal gland to check for cancer cells.
Not all adrenal tumors are cancerous. Tumors that have not grown beyond the adrenal gland may be benign (not cancer).
Staging and outlook for adrenal cancer
After a cancer diagnosis, staging gives your healthcare team important information about the extent of cancer in your body and your expected response to treatment.
The cancer stage describes how far cancer has spread in the body. It helps determine how serious the cancer is, what treatment options are available, and what to expect going forward. Your healthcare team will determine the stage of your cancer and use that to help guide your treatment plan.
Your cancer care team also uses a cancer’s stage when talking about survival statistics.
Adrenal cancer staging
Two major staging systems are used for adrenal cancer. They are the American Joint Committee on Cancer (AJCC) TNM staging system and the ENSAT (European Network for the Study of Adrenal Tumors) staging system. Both are based on the same TNM categories, which include 3 key pieces of information:
- T (tumor) describes the size of the main tumor and whether it has grown into nearby areas.
- N (nodes) describes the extent of spread to nearby (regional) lymph nodes).
- M (metastasis) indicates if the cancer has spread to distant parts of the body, such as other organs or lymph nodes that are not near the adrenal gland.
Numbers or letters after T, N, and M provide more details about each of these factors. Higher numbers mean the cancer is more advanced.
Once a person’s T, N, and M categories have been determined this information is combined in a process called stage grouping. This is usually done after surgery. This assigns an overall stage.
Adrenal cancer stages range from stages I through IV. The lower the number, the less the cancer has spread. A higher number, such as stage IV, means a more advanced cancer. Cancers with similar stages tend to have a similar outlook and are often treated in similar ways.
Adrenal cancer staging can be complex. If you have any questions about your stage, talk with your doctor or care team.
Stage grouping: T1, N0, M0
- The tumor is 5 cm (about 2 inches) or less in size.
- It has not grown into tissues outside the adrenal gland (T1).
- The cancer has not spread to nearby lymph nodes (N0) or distant sites (M0).
Stage grouping: T2, N0, M0
- The tumor is greater than 5 cm (2 inches) in size.
- It has not grown into tissues outside the adrenal gland (T2).
- The cancer has not spread to nearby lymph nodes (N0) or distant sites (M0).
Stage grouping: T1, N1, M0
- The tumor is 5 cm (about 2 inches) or smaller.
- It has not grown into tissues outside the adrenal gland (T1).
- The cancer has spread to nearby lymph nodes (N1) but not to distant sites (M0).
Stage grouping: T2, N1, M0
- The tumor is bigger than 5 cm (about 2 inches).
- It has not grown into tissues outside the adrenal gland (T2).
- The cancer has spread to nearby lymph nodes (N1) but not to distant sites (M0).
Stage grouping: T3, Any N, M0
- The tumor can be any size.
- The tumor is growing in the tissue that surrounds the adrenal gland (T3).
- The cancer might or might not have spread to nearby lymph nodes (Any N).
- The cancer has not spread to distant sites (M0).
Stage grouping: T4, Any N, M0
- The tumor can be any size.
- The tumor is growing into nearby organs, such as the kidney, pancreas, spleen, and liver or large blood vessels (renal vein or vena cava) (T4).
- The cancer may or may not have spread to nearby lymph nodes (Any N).
- The cancer has not spread to distant organs (M0).
Stage grouping: Any T, Any N, M1
- The tumor can be any size (Any T).
- The cancer may or may not have spread to nearby organs, large blood vessels, or tissues (Any T) or lymph nodes (Any N).
- The cancer has spread to distant sites like the liver or lungs (M1).
The following additional categories are not listed on the table above:
- TX: Main tumor cannot be assessed due to lack of information.
- T0: No evidence of a primary tumor.
- NX: Regional lymph nodes cannot be assessed due to lack of information.
Staging for children with adrenocortical carcinoma (ACC)
In children, the International Pediatric Adrenocortical Tumor Registry (IPACTR) System may be used for staging. In this system, stage is based on the size of the tumor, surgery outcome, hormone levels after surgery, and whether the cancer has spread to distant sites.
IPACTR stage |
Stage description |
I |
Small tumors (less than 100 grams) that were removed completely with surgery. Hormone levels after surgery are normal. |
II |
Large tumors (more than 100 grams) or tumors that ruptured during surgery. Hormone levels after surgery are normal. |
III |
Tumors cannot be removed completely with surgery, or tumors are removed but hormone levels remain abnormal. |
IV |
Tumors have spread to distant areas of the body. |
Outlook and survival rates for adrenal cancer
Cancer professionals use a cancer’s stage when talking about survival statistics. Survival rates are a way to measure how many people survive a certain type and certain stage of cancer over time. Some people find this information helpful, while others prefer to focus more on treatment plans and next steps.
Questions to ask if you have adrenal cancer
These questions can help you understand your diagnosis and what it means for you.
Understanding your diagnosis
- How sure are you that my tumor is cancer?
- Where is the cancer located? How big is it?
- What is the stage of the cancer? What does this mean?
- Will I need any other tests before we can decide on treatment?
- What is my prognosis (outlook), based on what you know about my cancer?
Talking about treatment
- Do I need to see any other doctors or health professionals?
- Who will be on my treatment team, and what will they do?
- Is this type of adrenal cancer hereditary? Should I consider genetic testing?
- Are there any clinical trials we should consider? How can we find out more about them?
- Should I get a second opinion? How do I do that? Can you recommend a doctor or cancer center?
- If I’m concerned about the costs and insurance coverage for my diagnosis and treatment, who can help me?
- Written by
- References
Developed by the American Cancer Society medical and editorial content team with medical review and contribution by the American Society of Clinical Oncology (ASCO).
American Joint Committee on Cancer. Adrenal Cortical. In: AJCC Cancer Staging Manual. 8th ed. New York: Springer. 2017:911-918.
Asban A, Patel AJ, Reddy S, Wang T, Balantine CJ, Chen H. Chapter 68: Cancer of the Endocrine System. In: Niederhuber JE, Armitage JO, Dorshow JH, Kastan MB, Tepper JE, eds. Abeloff’s Clinical Oncology. 6th ed. Philadelphia, Pa. Elsevier: 2020.
Lacroix A. Clinical Manifestations and diagnosis of adrenocortical carcinoma. UpToDate. 2026. Accessed at https://www.uptodate.com/contents/clinical-manifestations-and-diagnosis-of-adrenocortical-carcinoma on June 23, 2026.
National Cancer Institute. Adrenocortical Carcinoma Treatment (PDQ). Accessed at https://www.cancer.gov/types/adrenocortical/hp/adrenocortical-treatment-pdq on June 23, 2026.
National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Neuroendocrine and Adrenal Tumors Version 1.2026 – April 21, 2026. Accessed at https://www.nccn.org/professionals/physician_gls/pdf/neuroendocrine.pdf on June 23, 2026.
Rodriguez-Galindo C, Figueiredo BC, Zambetti GP, Ribeiro RC. Biology, clinical characteristics, and management of adrenocortical tumors in children. Pediatr Blood Cancer. 2005;45(3):265-273.
Young WF. Clinical Manifestations and diagnosis of pheochromocytoma. UpToDate. 2026. Accessed at https://www.uptodate.com/contents/clinical-presentation-and-diagnosis-of-pheochromocytoma on June 23, 2026.
Last Revised: October 5, 2026
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