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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Detalles Bibliográficos
Autores principales: Igaki, Junko, Nishi, Akira, Sato, Takeshi, Hasegawa, Tomonobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2018
Materias:
Case Report
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

Internet

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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