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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...
Autores principales: | Jacobson, Aaron, Koberlein, Elaine, Thomay, Alan, Lombard, Cara B, Adelanwa, Ayodele, Lakhani, Dhairya A, Smith, Kelly T. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
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 |
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