Adrenocortical carcinoma: the range of appearances on CT and MRI.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 21606258.
- Also identified by DOI 10.2214/AJR.10.5540.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Adrenocortical carcinoma (ACC) is a rare, aggressive tumor arising from the adrenal cortex that typically presents late with a large mass. The increased use of cross-sectional imaging for unrelated reasons has led to a greater number of ACCs being detected incidentally at an earlier stage. Recognition of the typical clinical, biochemical, and imaging findings is imperative for rapid diagnosis, prompt intervention, and early use of the appropriate therapy. Cross-sectional imaging with CT and MRI is essential for determining the extent of local and distant tumor spread. Complete surgical resection is currently the only potentially curative treatment of ACC, and the information attained from CT and MRI is important to guide surgery and further patient management.
Medical subject headings
- Adrenal Cortex Neoplasms
- Adrenocortical Carcinoma
- Magnetic Resonance Imaging
- Tomography, X-Ray Computed