Disease | von hippel-lindau syndrome |
Phenotype | C0206754|neuroendocrine tumors |
Sentences | 3 |
PubMedID- 25185468 | Background: management of pancreatic neuroendocrine tumors (pnets) associated with von hippel-lindau disease (vhl) is challenging because of the malignant potential and difficulty in predicting prognosis. |
PubMedID- 26489587 | [a case of von hippel-lindau disease with nonfunctioning pancreatic neuroendocrine tumors treated by duodenum-preserving resection of the head of the pancreas and spleen-preserving resection of the tail of the pancreas]. |
PubMedID- 24921213 | Use of sunitinib in a 30-year-old woman with pancreatic neuroendocrine tumors associated with von hippel-lindau syndrome. |
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