Parathyroid Cancer in the Pediatric Patient. Issue 1 (January 2016)

• Record Type: Journal Article
• Authors: Davidson, Jesse T.; Lam, Catherine G.; McGee, Rose B.; Bahrami, Armita; Diaz-Thomas, Alicia
• Is Part Of: Journal of pediatric hematology/oncology. Volume 38:Issue 1(2016)
• Publication Date: 2016-01
• Subjects: pediatric -- child -- parathyroid carcinoma -- parathyroid cancer -- hyperparathyroidism -- CDC73; Pediatric hematology -- Periodicals; Tumors in children -- Periodicals; 618.9215
• DOI: 10.1097/MPH.0000000000000443
• Languages: English
• ISSNs: 1077-4114

Abstract

Abstract : Context: Parathyroid carcinoma is exceedingly rare in children. We describe a case of parathyroid cancer in a young female who was originally classified as benign and managed surgically. Upon her diagnosis with malignancy, concurrent with metastatic lung involvement, she was referred for medical and surgical palliation to control her symptomatic hypercalcemia. We briefly review published childhood cases, consider the challenges in differentiating malignant from benign hyperparathyroidism in this age group, and discuss the association of CDC73 mutations with parathyroid carcinoma. Case Presentation: A 13-year-old African American girl with a history of parathyroid adenoma, diagnosed at 8 years of age with multiple recurrences, presented with hypercalcemia and elevated parathyroid hormone when her disease had been reclassified as malignant. Germline gene analysis revealed a heterozygous partial deletion of CDC73 . The patient underwent palliative surgery for disease metastatic to her lungs. She continues with medical management of her hypercalcemia. Conclusions: A case of pediatric parathyroid carcinoma associated with haploinsufficiency of CDC73 is discussed. We review all published cases of pediatric parathyroid carcinoma and offer diagnostic considerations for a parathyroid mass in a child.