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A malignant pheochromocytoma in a child with von Hippel-Lindau mutation
Pheochromocytoma is a rare neuroendocrine tumor that arises from the chromaffin cells of the sympathetic nervous system. Over one third of pheochromocytomas are associated with germline mutations. We describe a 3 year-old girl with an inherited right adrenal malignant pheochromocytoma, with the moth...
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| Publicado no: | Clujul Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Iuliu Hatieganu University of Medicine and Pharmacy
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5536217/ https://ncbi.nlm.nih.gov/pubmed/28781534 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15386/cjmed-760 |
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