Results 151 to 160 of about 26,263 (201)
Parathyroid carcinoma and pheochromocytoma in a patient with neurofibromatosis type 1: a rare association. [PDF]
Endocrinol Diabetes Metab Case RepLeite JBR +11 more
europepmc +1 more source
An explainable radiomics-based machine learning model for preoperative differentiation of parathyroid carcinoma and atypical tumors on ultrasound: a retrospective diagnostic study. [PDF]
Front Endocrinol (Lausanne)Liu C +10 more
europepmc +1 more source
Current Treatment Options in Oncology, 2001 Although parathyroid neoplasms are common and cause primary hyperparathyroidism, parathyroid carcinoma is a rare entity. At times it can be difficult to diagnose. Patients with parathyroid carcinoma usually present with profound symptoms of hyperparathyroidism and highly elevated serum calcium and parathyroid hormone (PTH) levels.
Electron Kebebew, Kebebew Electron
exaly +10 more sources
Best Practice and Research in Clinical Endocrinology and Metabolism, 2018 Parathyroid carcinoma (PC) is a rare disease with an indolent behavior due to the low malignant potential. The etiology is unknown. Somatic mutations of CDC73 gene, the same gene involved in the hyperparathyroidism-jaw tumor syndrome, can be identified in up to 70% of patients with PC and in one-third of cases the mutations are germline.
Antonio Stefano Salcuni +2 more
exaly +6 more sources
Parathyroid carcinoma in a child
Journal of Pediatric Surgery, 1999 Parathyroid carcinoma is a rare cause of hypercalcemia in children but should be considered in a child presenting with an extremely elevated serum calcium level. The authors report the fifth case of parathyroid carcinoma in a child less than 16 years of age.
Donald E Meier +2 more
exaly +4 more sources