Adrenocortical carcinoma
Tumor - adrenal; ACC - adrenal
Adrenocortical carcinoma (ACC) is a cancer of the adrenal glands. The adrenal glands are two triangle-shaped glands. One gland is located on top of each kidney.
Causes
ACC is most common in children younger than 5 years old and adults in their 40s and 50s.
The condition may be linked to a cancer syndrome that is passed down through families (inherited). Both men and women can develop this tumor.
ACC can produce the hormones cortisol, aldosterone, estrogen, or testosterone, as well as other hormones. In women the tumor often releases these hormones, which can lead to male characteristics.
ACC is very rare. The cause is unknown.
Symptoms
Symptoms of increased cortisol or other adrenal gland hormones may include:
- Fatty, rounded hump high on the back just below the neck (buffalo hump)
- Flushed, rounded face with pudgy cheeks (moon face)
- Obesity
- Stunted growth (short stature)
- Virilization -- the appearance of male characteristics, including increased body hair (especially on the face), pubic hair, acne, deepening of the voice, and enlarged clitoris (females)
Symptoms of increased aldosterone are the same as symptoms of low potassium, and include:
- Muscle cramps
- Weakness
- Pain in the abdomen
Exams and Tests
The health care provider will perform a physical exam and ask about your symptoms.
Blood tests will be done to check hormone levels:
- ACTH level will be low.
- Aldosterone level will be high.
- Cortisol level will be high.
- Potassium level will be low.
- Male or female hormones may be abnormally high.
Imaging tests of the abdomen may include:
- Ultrasound
- CT scan
- MRI
- PET scan
Treatment
Primary treatment is surgery to remove the tumor. ACC may not improve with chemotherapy. Medicines may be given to reduce production of cortisol, which causes many of the symptoms.
Outlook (Prognosis)
The outcome depends on how early the diagnosis is made and whether the tumor has spread (metastasized). Tumors that have spread usually lead to death within 1 to 3 years.
Possible Complications
The tumor can spread to the liver, bone, lung, or other areas.
When to Contact a Medical Professional
Contact your provider if you or your child has symptoms of ACC, Cushing syndrome, or failure to grow.
References
Allolio B, Fassnacht M. Adrenocortical carcinoma. In: Jameson JL, De Groot LJ, de Kretser DM, et al, eds. Endocrinology: Adult and Pediatric. 7th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 107.
National Cancer Institute website. Adrenocortical carcinoma treatment (Adult) (PDQ) - health professional version. www.cancer.gov/types/adrenocortical/hp/adrenocortical-treatment-pdq. Updated August 25, 2022. Accessed October 14, 2022.
Yeh MW, Livhits M, Duh Q-Y. The adrenal glands. In: Townsend Jr CM, Beauchamp RD, Evers DM, Mattox KL, et al, eds. Sabiston Textbook of Surgery. 21st ed. St Louis, MO: Elsevier; 2022:chap 40.
Endocrine glands - illustration
Endocrine glands
illustration
Adrenal metastases - CT scan - illustration
Adrenal metastases - CT scan
illustration
Adrenal Tumor - CT - illustration
Adrenal Tumor - CT
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Review Date: 8/15/2022
Reviewed By: Todd Gersten, MD, Hematology/Oncology, Florida Cancer Specialists & Research Institute, Wellington, FL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
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