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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Hlavní autoři: Zografos, George N, Vasiliadis, George K, Zagouri, Flora, Aggeli, Chrysanthi, Korkolis, Dimitris, Vogiaki, Sophia, Pagoni, Matina K, Kaltsas, Gregory, Piaditis, George
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2010
Témata:
Case Report
On-line přístup: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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