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Adrenocortical Carcinoma

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Adrenal tumors can be adrenal incidentalomas, adenomas, adrenocortical carcinoma (ACC), or pheochromocytoma (malignant or benign). Making up the majority of adrenal tumors are benign, nonfunctioning (not producing hormones) adenomas that are discovered incidentally on abdominal imagining studies referred to as adrenal incidentalomas. Another large part of adrenal tumors are benign, functioning (secreting hormones) adenomas. From most frequent to least, these functioning adrenal adenomas can cause Cushing’s syndrome, primary aldosteronism, and virilization. Adrenocortical carcinomas (ACCs) are the least common among adrenal tumors but are extremely heterogeneous and can be aggressive and fatal. Evaluation of adrenal incidentalomas and adrenocortical adenomas are discussed briefly here. This chapter will focus on adrenocortical carcinomas (ACCs), discussing all aspects of ACCs including management and treatment of this rarest disease.

Original languageEnglish (US)
Title of host publicationCurrent Clinical Oncology
PublisherSpringer International Publishing
Pages195-220
Number of pages26
DOIs
StatePublished - 2011

Publication series

NameCurrent Clinical Oncology
VolumePart F5177
ISSN (Print)2364-1134
ISSN (Electronic)2364-1142

Keywords

  • Adrenal incidentalomas
  • Adrenocortical adenomas
  • Adrenocortical carcinoma
  • Cushing’s syndrome
  • Pheochromocytoma
  • Primary aldosteronism
  • Virilization

ASJC Scopus subject areas

  • Oncology
  • Cancer Research
  • Pathology and Forensic Medicine
  • Oncology(nursing)

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