eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pheochromocytoma |
| Comorbidity | C0206754|neuroendocrine tumor |
| Sentences | 3 |
| PubMedID- 22799452 | Von hippel-lindau (vhl) disease (omim 193300) is a dominantly inherited cancer syndrome characterized by central nervous system and retinal hemangioblastomas, clear cell renal carcinoma, neuroendocrine tumors and cysts of the pancreas, pheochromocytomas, endolymphatic sac tumors and/or papillary cystadenomas of the epididymis and broad ligament [1]. |
| PubMedID- 22145148 | Histology was diagnostic for pheochromocytoma with a neuroendocrine tumor of the pancreas. |
| PubMedID- 20560986 | We contribute an additional case of bilateral pheochromocytoma combined with early-onset neuroendocrine tumor of the pancreas to the literature. |
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