Duodenal neuroendocrine tumour in a young patient with von Recklinghausen disease

Von Recklinghausen disease (neurofibromatosis type 1—NFT1) is a genetic disorder with autosomal dominant inheritance pattern, caused by mutation of a tumour suppressor gene. Its main features include multiple cutaneous café-au-lait spots and neurofibromas. It is associated with an increased risk of...

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Detalles Bibliográficos
Autores principales: Leite, Cláudia, Constantino, Júlio, Melo Pinto, Daniela, Pinto, José Carlos, Sá, Milene, Pereira, Jorge, Casimiro, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054206/
https://www.ncbi.nlm.nih.gov/pubmed/32153765
http://dx.doi.org/10.1093/jscr/rjaa039

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054206/
https://www.ncbi.nlm.nih.gov/pubmed/32153765
http://dx.doi.org/10.1093/jscr/rjaa039

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