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Up to: Hereditary disease · Adenocarcinoma · Malignant tumor of parathyroid gland

Parathyroid gland carcinoma

A 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.

4 trials tagged with this condition →

This condition has no sub-types.