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Giant adrenal myelolipoma in a young female patient: a case report

Myelolipoma is a rare, benign, non-secreting tumor and its pathophysiology is of metaplasia of the cells of the adrenal cortex into reticuloendothelial cells. Although they are often small and asymptomatic, some cases of giant adrenal myelolipoma cause symptoms such as chronic pain. Few cases of adr...

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Detalles Bibliográficos
Autores principales: Rahoui, Moez, Ouanes, Yassine, Chaker, Kays, Dali, Kheireddine Mrad, Bibi, Mokhtar, Sellami, Ahmed, Rhouma, Sami Ben, Nouira, Yassine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9155172/
https://www.ncbi.nlm.nih.gov/pubmed/35665404
http://dx.doi.org/10.1093/jscr/rjac213
Descripción
Sumario:Myelolipoma is a rare, benign, non-secreting tumor and its pathophysiology is of metaplasia of the cells of the adrenal cortex into reticuloendothelial cells. Although they are often small and asymptomatic, some cases of giant adrenal myelolipoma cause symptoms such as chronic pain. Few cases of adrenal myelolipoma have been reported in the literature. We present a case of a large right adrenal myelolipoma in a 26-year-old female patient, who presented with an adrenal mass, and discuss the challenges of diagnosis and treatment.