Adrenocortical epithelial neoplasia with intense cellular pleomorphism in a young patient: A case report
DOI:
https://doi.org/10.56238/isevjhv3n2-001Palabras clave:
Adrenocortical, Cellular pleomorphism, Carcinoma.Resumen
Adrenocortical epithelial neoplasms represent a diverse spectrum of tumors originating in the adrenal cortex, such as adrenal cortical carcinomas (ACCs) and adrenal cortical adenomas (ACAs), which are rare but clinically significant tumors. The aim of this article is to report the clinical case of a 29-year-old patient who was affected by an adrenocortical epithelial neoplasm with intense cellular pleomorphism. Surgical treatment was performed urgently to resolve the initial condition, and the diagnosis was aided by imaging and anatomopathological methods.
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2024-03-18
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Brambila Jorge Pareja, H., Dale Vedove Rosa, G., Rezende de Lima, M., de Souza Camargo, M., Padovam Cavalcante, L., Isaac Grassi Evangelista, N., Eduarda Henrique de Mello Pelegrini, M., & Beraldo Bueno Fonseca, A. (2024). Adrenocortical epithelial neoplasia with intense cellular pleomorphism in a young patient: A case report. International Seven Journal of Health Research, 3(2), 382–388. https://doi.org/10.56238/isevjhv3n2-001
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