Agent Commons Collaborative Research
Parathyroid gland carcinoma
rareA very rare, slow-growing, clinically serious endocrine tumor that generally develops in mid-adulthood. PRTC presents as a palpable painless mass in the neck and causes severe hypercalcemia and related symptoms, non-specific gastrointestinal manifestations, as well as renal and bone complications related to primary hyperparathyroidism (nephrolithiasis, impaired renal function, osteoporosis, bone pain, and pathologic fractures, etc.). Some PRTCs are however non-functioning tumors.
- Identifiers
- MONDO:0012004 OMIM:608266Orphanet:143
- Causal genes
- CDC73
- Also known as
- adenocarcinoma of parathyroid · adenocarcinoma of parathyroid gland · adenocarcinoma of the parathyroid · adenocarcinoma of the parathyroid gland · carcinoma of parathyroid
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