Definition | Causes | Risk Factors | Symptoms | Diagnosis | Treatment | Prevention

Symptoms

Approximately 40% of adrenocortical carcinoma do not secrete any hormone. These people do not have any specific symptoms. Adrenocortical carcinoma is discovered either by accident or as part of a physical examination for abdominal pain.

Other tumors are hormonally active (functional). Excess hormones may produce symptoms such as:

Other conditions that may result from functional tumors of the adrenal cortex include:

  • Cushing’s syndrome (Hypercortisolism)—30% of cases—excess cortisol which helps the body respond to stressful situations and infections
  • Conn’s syndrome (Hyperaldosteronism)—2% of cases—excess aldosterone, which helps the body maintain normal levels of sodium and potassium
  • Virilization (20% of cases)—women with functional tumors that release males hormones; may deepen voice, cause hirsutism (growing excess hair on the face), and swelling of the sex organs or breasts may occur
  • A mixed Cushing’s syndrome and virilization accounts for 35% of all cases
  • In young children with functional tumors that release sex hormones, these tumors may cause early onset of puberty

These symptoms may be caused by other health conditions. Anyone experiencing these symptoms should see a doctor.

Diagnosis

Your doctor will ask about your symptoms, and medical and family history. A physical exam will be done.

Tests may include the following:

After cancer of the adrenal cortex is confirmed, you will be referred to an oncologist. This type of doctor focuses on cancer.

Additional testing will be done to determine what stage (1-4) the cancer has reached. The stage of a tumor is determined by its size and how far it has spread from its point of origin. At the time of diagnosis, 30%-85% of patients are found to have cancer that has spread. The higher the stage, the more dangerous and difficult it is to treat.