Adrenocortical carcinoma (ACC) is a rare malignancy that is generally associated with a poor prognosis whose existence dictates the management of incidental renal masses. We report a case of ACC diagnosed and treated at its apparent inception in a patient undergoing close surveillance imaging of a prior malignancy. Despite timely detection and resection of a localized ACC this patient rapidly progressed to systemic disease. This case highlights the rapid growth kinetics of ACC and puts into perspective the challenges associated with the established treatment paradigm for patients diagnosed with an adrenal mass.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011172 | PMC |
http://dx.doi.org/10.1016/j.eucr.2016.07.009 | DOI Listing |
Clin Chem
January 2025
Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Clin Chem
January 2025
Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, United States.
Clin Chem
January 2025
Division of Cancer Research, Peter MacCallum Cancer Centre, Melbourne, Australia.
Surgery
December 2024
Department of Surgery, Weill Cornell Medicine, New York, NY.
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