Rare triad of periampullary carcinoid, duodenal gastrointestinal stromal tumor and plexiform neurofibroma at hepatic hilum in neurofibromatosis type 1: a case report

Abstract Background Neurofibromatosis type 1 is a relatively common inherited disorder. Patients with neurofibromatosis type 1 are at high risk of developing neurogenic, neuroendocrine and mesenchymal intra-abdominal tumors. Although coexistence of multiple tumors of different types is frequent in n...

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Principais autores:	Nihed Abdessayed, Rahul Gupta, Sarra Mestiri, Ahlem Bdioui, Mounir Trimech, Moncef Mokni
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BMC 2017-08-01
סדרה:	BMC Cancer
נושאים:	Case report Neurofibromatosis Neuroendocrine tumor Gastrointestinal stromal tumor Neurofibroma Whipple’s operation
גישה מקוונת:	http://link.springer.com/article/10.1186/s12885-017-3567-z
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