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PedAM

Pediatric Disease Annotations & Medicines




Disease neuroendocrine tumor
Phenotype C0019562|hippel-lindau disease
Sentences 2
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- 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.

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