Adrenocortical epithelial neoplasia with intense cellular pleomorphism in a young patient: A case report

Autores/as

  • Helen Brambila Jorge Pareja
  • Guilherme Dale Vedove Rosa
  • Moabe Rezende de Lima
  • Matheus de Souza Camargo
  • Leonardo Padovam Cavalcante
  • Nathan Isaac Grassi Evangelista
  • Maria Eduarda Henrique de Mello Pelegrini
  • Amanda Beraldo Bueno Fonseca

DOI:

https://doi.org/10.56238/isevjhv3n2-001

Palabras 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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Publicado

2024-03-18

Cómo citar

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

Número

Vol. 3 Núm. 2 (2024): March/April - 2024

Sección

Articles