PedAM
Pediatric Disease Annotations & Medicines
| Disease | multiple endocrine neoplasia |
| Phenotype | C0242363|pancreatic endocrine tumor |
| Sentences | 4 |
| PubMedID- 22584720 | Surgical approaches to pancreatic endocrine tumors associated with multiple endocrine neoplasia type 1 may differ greatly from those applied to sporadic pancreatic endocrine tumors. |
| PubMedID- 22797396 | Context: the surgical management of pancreatic endocrine tumors in patients with multiple endocrine neoplasia type 1 (men-1) is controversial and complicated by the fact that these tumors are frequently multifocal. |
| PubMedID- 22123505 | Multiple pancreatic masses have been reported as follows: metastatic pancreatic tumor such as renal cell carcinoma, pancreatic endocrine tumor with multiple endocrine neoplasia type 1 (men1), von hippel–lindau (vhl) disease, autoimmune pancreatitis, and intraductal pancreatic mucinous neoplasm[11–15]. |
| PubMedID- 23645327 | To accomplish these comparisons, we searched medline (national library of medicine, bethesda, md) using the key words men1 or multiple endocrine neoplasia combined with gastrinoma, pancreatic endocrine tumor, glucagonoma, zollinger-ellison syndrome, thymic carcinoid, hpt, death, survival, and pituitary tumor, either alone or in combination. |
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