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

Autor: Ahmed AA; Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA., Thomas AJ; Department of Radiology, Baylor College of Medicine, Houston, TX, USA., Ganeshan DM; Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA., Blair KJ; Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA., Lall C; Department of Radiology, University of Florida College of Medicine, Jacksonville, FL, USA., Lee JT; Department of Radiology, University of Kentucky, Lexington, Kentucky, USA., Morshid AI; Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA., Habra MA; Departments of Endocrine Neoplasia and Hormonal Disorders, University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA., Elsayes KM; Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Houston, TX, 77030, USA. kmelsayes@mdanderson.org.
Jazyk: angličtina
Zdroj: Abdominal radiology (New York) [Abdom Radiol (NY)] 2020 Apr; Vol. 45 (4), pp. 945-963.
DOI: 10.1007/s00261-019-02371-y
Abstrakt: 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.
Databáze: MEDLINE
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