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Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern
Somatostatinoma is a very rare neuroendocrine tumor that originates from D cells and accounts for less than 1% of all gastrointestinal endocrine tumors. The duodenum is the most frequent site for this tumor, followed by the pancreas. We here describe a 46-year-old Chinese woman who developed pancrea...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Zhejiang University Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2801086/ https://ncbi.nlm.nih.gov/pubmed/20043348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.B0900166 |
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