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Fever of Unknown Origin: Could It Be a Pheochromocytoma? A Case Report and Review of the Literature
Pheochromocytomas are rare tumors that arise from the adrenal medulla, with an incidence of less than 1 per 100,000 person-years. These tumors are characterized by excess catecholamine secretion and classically present with the triad of headaches, palpitations, and sweating episodes. However, the cl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051277/ https://www.ncbi.nlm.nih.gov/pubmed/30057828 http://dx.doi.org/10.1155/2018/3792691 |