Congenital adrenal hyperplasia with associated giant adrenal myelolipoma, testicular adrenal rest tumors and primary pigmented nodular adrenocortical disease: A case report and brief review of the literature

Congenital adrenal hyperplasia is an autosomal recessive disease most commonly associated with 21-hydroxylase deficiency, an enzyme integral in the biosynthesis of mineralocorticoids and glucocorticoids. We present a case of a 49-year-old male with congenital adrenal hyperplasia and commonly associa...

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Detalles Bibliográficos
Autores principales: Jacobson, Aaron, Koberlein, Elaine, Thomay, Alan, Lombard, Cara B, Adelanwa, Ayodele, Lakhani, Dhairya A, Smith, Kelly T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718818/
https://www.ncbi.nlm.nih.gov/pubmed/35003466
http://dx.doi.org/10.1016/j.radcr.2021.12.031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718818/
https://www.ncbi.nlm.nih.gov/pubmed/35003466
http://dx.doi.org/10.1016/j.radcr.2021.12.031

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