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PedAM

Pediatric Disease Annotations & Medicines




Disease von hippel-lindau syndrome
Phenotype C0206754|neuroendocrine tumor
Sentences 5
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- 23205114 Clear cell neuroendocrine tumor g1 of the gallbladder without von hippel-lindau disease.
PubMedID- 24921213 Use of sunitinib in a 30-year-old woman with pancreatic neuroendocrine tumors associated with von hippel-lindau syndrome.
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- 22415670 Long-term disease control with sunitinib in a patient with metastatic pancreatic neuroendocrine tumor (net) associated with von hippel-lindau syndrome (vhl).

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