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Pheochromocytoma associated with neurofibromatosis type 1: concepts and current trends
BACKGROUND: Neurofibromatosis Type 1(NF-1) has autosomal dominant inheritance with complete penetrance, variable expression and a high rate of new mutation. Pheochromocytoma occurs in 0.1%-5.7% of patients with NF-1. CASE PRESENTATION: We present the case of a 37-year-old patient with laparoscopical...
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| Autori principali: | , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2848134/ https://ncbi.nlm.nih.gov/pubmed/20219130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1477-7819-8-14 |
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