Update on Adrenocortical Carcinoma

Urol Clin North Am. 2025 May;52(2):275-286. doi: 10.1016/j.ucl.2025.01.009. Epub 2025 Mar 13.

Abstract

Adrenocortical carcinoma (ACC) is an uncommon and highly aggressive form of cancer that originates from the adrenal glands. It displays a dual age distribution pattern, with a higher occurrence during early childhood around the average age of 3.2 years, and a second peak in the fourth and fifth decades of adulthood. The diagnosis of ACC requires a multifaceted approach, with accurate risk assessment being crucial for effective treatment planning. This review article offers a comprehensive overview of ACC, encompassing its epidemiology, clinical presentation, diagnosis, prognostic factors, and treatment methodologies.

Keywords: Adrenal glands; Adrenocortical carcinoma; Adulthood; Cancer; Pathology.

Publication types

  • Review

MeSH terms

  • Adrenal Cortex Neoplasms* / diagnosis
  • Adrenal Cortex Neoplasms* / epidemiology
  • Adrenal Cortex Neoplasms* / therapy
  • Adrenocortical Carcinoma* / diagnosis
  • Adrenocortical Carcinoma* / epidemiology
  • Adrenocortical Carcinoma* / therapy
  • Humans
  • Prognosis