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Incidental Pheochromocytoma: Silent but Violent
Background: Pheochromocytoma is a rare catecholamine secreting neuroendocrine tumor. It arises from the chromaffin cells of adrenal medulla. It is diagnosed in 5–6.5% of adrenal incidentalomas which is not common. The usual clinical presentation includes the classic triad of sweating, headache and t...
Autores principales: | Bantu, Sravani, Vallepu, Shirisha R, Gunda, Mouna, Thudi, Vaishali |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089244/ http://dx.doi.org/10.1210/jendso/bvab048.277 |
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