Adrenal cancer, known as adrenocortical cancer, is a rare form of cancer that can form at the top of one or both of your adrenal glands (top of your kidneys). These glands are crucial in hormone production, influencing the functioning of nearly every organ and tissue in your body.
This type of cancer can affect individuals at any age, but it is most commonly seen in children under 5 and adults in their 40s and 50s. When detected early, there is a chance for a cure, but if the cancer has spread beyond the adrenal glands, the prospects for a complete cure are lowered. Treatment options are available to help manage and potentially delay the progression or recurrence of the disease.
It is worth noting that most growths in the adrenal glands are noncancerous, including benign tumours such as adenomas and pheochromocytomas.
The exact causes are not yet fully understood. However, recent advances in medical research have progressed on how specific DNA changes can trigger the development of cancerous cells within the adrenal gland. DNA influences both your physical traits and your susceptibility to certain diseases, including cancer.
Key genetic factors can include:
Although these DNA mutations can increase your cancer risk, in most cases, these mutations can occur in your lifetime without any discernible external trigger and only rarely cause adrenal cancer.
Symptoms include:
If you suspect you have symptoms or are concerned about your adrenal health, consult with an endocrinologist for a proper evaluation and diagnosis.
In the early stages, when the tumor size is small, it is completely painless and asymptomatic. The most common presentation would be a mass detected on imaging in the adrenal gland. In later stages, when the size enlarges or the tumor spreads to other structures, it can cause some degree of pain. As the adrenal cancer grows, it may exert pressure on nearby organs and tissues. This can cause discomfort near the tumour, a sense of abdominal fullness, and/or difficulty eating due to feeling full faster than usual.
The extent of pain and discomfort you can feel varies between individuals and depends on the stage of your cancer and its spread.
This cancer can affect anyone. This can be of varying ages and backgrounds. While it is a rare form of cancer, several factors may increase your risk of developing the condition.
If you are experiencing symptoms and are concerned about your risk of developing it, make an appointment with ACE Specialist Surgery and Endoscopy to get proper medical assessments for early detection of cancer cell growth.
Adrenal cancer can be diagnosed in the following ways:
Treatment options largely depend on the stage of your cancer and the extent of it.
If you are suffering from an adrenal gland disorder, have a family history of adrenal disorders, or are concerned about developing adrenal cancer, schedule an appointment with ACE Surgery and Endoscopy for a detailed examination and individualised treatment plan.
In its early stages, adrenal cancer tumours may be surgically removed, and a patient’s 5-year survival rate is at least 50 to 60%. In cases where the cancer has spread to other organs, the 5-year survival rate decreases to 10 to 20%.
In its early stages, this cancer can be cured with surgery with a 50 to 60% chance of at least a 5-year survival rate. However, if the cancer is discovered after spreading to other organs (beyond the adrenal gland), it can impact your prognosis.
This cancer can be recurrent, especially near the original site or in distant organs (even after early-stage treatment). Closely monitoring any changes through follow-up care is crucial to detect and effectively manage any potential recurrence.