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A pediatric case of pheochromocytoma without apparent hypertension associated with von Hippel-Lindau disease
Pheochromocytomas are catecholamine-secreting tumors. These tumors are rare in children, and they may be associated with hereditary syndromes such as von Hippel-Lindau (VHL) disease. Most pediatric patients with pheochromocytoma present with sustained hypertension, while 10% to 69% of adult patients...
Autores principales: | Igaki, Junko, Nishi, Akira, Sato, Takeshi, Hasegawa, Tomonobu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society for Pediatric Endocrinology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897584/ https://www.ncbi.nlm.nih.gov/pubmed/29662268 http://dx.doi.org/10.1297/cpe.27.87 |
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