Cargando…
Inhibin A as a tumor marker for primary bilateral macronodular adrenal hyperplasia
SUMMARY: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of ACTH-independent Cushing syndrome (CS). This condition is characterized by glucocorticoid and/or mineralocorticoid excess, and is commonly regulated by aberrant G-protein coupled receptor expression may be subclin...
Autores principales: | Wurth, Rachel, Kamilaris, Crystal, Nilubol, Naris, Sadowski, Samira M, Berthon, Annabel, Quezado, Martha M, Faucz, Fabio R, Stratakis, Constantine A, Hannah-Shmouni, Fady |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219132/ https://www.ncbi.nlm.nih.gov/pubmed/32478669 http://dx.doi.org/10.1530/EDM-20-0006 |
Ejemplares similares
-
OR02-6 Mass Spectrometry-Based Steroid Profiling Inprimary Bilateral Macronodular Adrenocortical Hyperplasia
por: Hannah-Shmouni, Fady, et al.
Publicado: (2019) -
(18)F-FDOPA PET/CT accurately identifies MEN1-associated pheochromocytoma
por: Tepede, Aisha A, et al.
Publicado: (2020) -
Long-term low-dose ketoconazole treatment in bilateral macronodular adrenal hyperplasia
por: Comte-Perret, Sophie, et al.
Publicado: (2014) -
Feminizing adrenal tumor identified by plasma steroid profiling
por: Vogt, Elinor Chelsom, et al.
Publicado: (2021) -
Urinary steroid profiling in diagnostic evaluation of an unusual adrenal mass
por: Lenders, N F, et al.
Publicado: (2019)