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Transition of a pancreatic neuroendocrine tumor from ghrelinoma to insulinoma: a case report

Pancreatic neuroendocrine tumors (PNETs) are rare with an incidence of 1 in 100,000 populations. PNETs can present either as a functional or non-functional tumor. In functional tumors the symptoms are a result of hormones such as insulin, gastrin, glucagon and vasoactive intestinal peptide (VIP) or...

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Dettagli Bibliografici
Pubblicato in:J Gastrointest Oncol
Autori principali: Chauhan, Aman, Ramirez, Robert A., Stevens, Melissa A., Burns, Leigh Anne, Woltering, Eugene A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: AME Publishing Company 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4311091/
https://ncbi.nlm.nih.gov/pubmed/25830049
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2078-6891.2014.113
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