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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...
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| Publicado no: | Clin Pediatr Endocrinol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Japanese Society for Pediatric Endocrinology
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5897584/ https://ncbi.nlm.nih.gov/pubmed/29662268 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.27.87 |
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