ea0037ep1128 | Endocrine tumours | ECE2015
Bogusz Pawel
, McConnell Elizabeth Mae
, McConnell Vivienne
, Korda Marian
Hyperparathyroidism-jaw tumour syndrome (HPT-JT) is a rare autosomal dominant condition characterized by primary hyperparathyroidism (<90%) as a result of parathyroid adenoma or carcinoma (1015%), ossifying fibromas of mandible and maxilla (3040%), renal lesions (20%) most commonly cysts and benign and malignant uterine tumours and caused by germline CDC73 pathogenic gene mutations. Currently only 200 cases reported in medical literature. His management has pro...