eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | medullary thyroid carcinoma |
| Comorbidity | C0031511|pheochromocytoma |
| Sentences | 5 |
| PubMedID- 20951316 | Men type 2 (men2) conditions represent at least four different syndromes that associate pheochromocytoma with medullary thyroid carcinoma, hyperparathyroidism, and a number of other manifestations. |
| PubMedID- 24899893 | For instance, the presence of hemangioblastomas (suggestive of von hippel-lindau) or medullary thyroid carcinoma along with pheochromocytoma (suggestive of men 2a) strongly implies mutations in vhl or ret gene, respectively [27, 29]. |
| PubMedID- 22540085 | Men type 2 (men2) conditions represent at least four different syndromes that associate pheochromocytoma with medullary thyroid carcinoma, hyperparathyroidism, and a number of other manifestations. |
| PubMedID- 25374962 | We report a 54-year-old man with a men-2a which presents with a nonfunctional metastatic parathyroid carcinoma and a pheochromocytoma in the absence of medullary thyroid carcinoma. |
| PubMedID- 23569534 | Men2a presents as a medullary thyroid carcinoma with bilateral pheochromocytoma and hyperplasia of the parathyroid gland, and men2b is characterized by the additional appearance of neurocutaneous manifestations without primary hyperparathyroidism. |
Page: 1