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

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, pat...

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Detalles Bibliográficos
Publicado en:Abdominal Radiology Vol. 45; no. 4; pp. 945 - 964
Autores principales: Ahmed, Ayahallah A., Thomas, Aaron J., Ganeshan, Dhakshina Moorthy, Blair, Katherine J., Lall, Chandana, Lee, James T., Morshid, Ali I., Habra, Mouhammed A., Elsayes, Khaled M.
Formato: Journal Article
Publicado: Springer Nature Apr2020
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario: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.