Adrenal Tumours

EA 3.3 Adrenal Tumours

Adrenal tumours are growths that develop in the adrenal glands, which are located on top of each kidney and are responsible for producing hormones that regulate blood pressure, metabolism, and the body’s response to stress. Adrenal tumours can be benign (non-cancerous) or malignant (cancerous). Benign tumours are more common and usually do not cause symptoms unless they are large or produce excess hormones. Malignant tumours can spread to other parts of the body and can cause symptoms such as abdominal pain, weight loss, and high blood pressure. Diagnosis of adrenal tumours usually involves blood tests to measure hormone levels, imaging tests, and sometimes a biopsy to examine a sample of the tumour tissue. Treatment for adrenal tumours depends on the type and size of the tumour, as well as the patient’s overall health. Treatment options may include surgery to remove the tumour, radiation therapy, chemotherapy, or medications to control hormone levels.

Expertise Area Coordinator and Vice-EAC

Expertise Area Coordinator:

Hans Langenhuijsen

Vice-EAC:

Nikola Knežević

Conditions and Codes

  • Benign neoplasm of pituitary gland: ICD-10 Code D35.2
  • Cushing syndrome: ICD-10 Codes E24.0, E24.8
  • Adrenogenital disorders: ICD-10 Code E25.0
  • Phakomatoses, not elsewhere classified: ICD-10 Code Q85.8
  • Von Hippel-Lindau disease: ORPHAcode 892
  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form: ORPHAcode 315311
  • Rare primary hyperaldosteronism: ORPHAcode 181415 / ICD-10 Code E26.0

Healthcare Providers

BE Leuven UZ, ES Barcelona Fundació Puigvert, ES Santander Valdecilla, HR Zagreb KBC, LT Vilnius SK, NL Nijmegen Radboudumc, SE Lund SUS

Additional Resources