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Abdom Radiol (NY). 2020 Jan 1. doi: 10.1007/s00261-019-02371-y. [Epub ahead of print]

Adrenal cortical carcinoma: pathology, genomics, prognosis, imaging features, and mimics with impact on management.

Author information

1
Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA.
2
Department of Radiology, Baylor College of Medicine, Houston, TX, USA.
3
Department of Radiology, University of Florida College of Medicine, Jacksonville, FL, USA.
4
Department of Radiology, University of Kentucky, Lexington, Kentucky, USA.
5
Departments of Endocrine Neoplasia and Hormonal Disorders, University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
6
Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA. kmelsayes@mdanderson.org.

Abstract

Adrenocortical carcinoma (ACC) is a rare tumor with a poor prognosis. Most tumors are either metastatic or locally invasive at the time of diagnosis. Differentiation between ACC and other adrenal masses depends on clinical, biochemical, and imaging factors. This review will discuss the genetics, pathological, and imaging feature of ACC.

KEYWORDS:

Adrenal cortical carcinoma; Adrenal tumors; CT adrenal protocol; Cushing syndrome; Ki67; MRI; Weiss score

PMID:
31894378
DOI:
10.1007/s00261-019-02371-y

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