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Primary hyperparathyroidism may masquerade as rickets-osteomalacia in vitamin D replete children.
- Source :
- Journal of Pediatric Endocrinology & Metabolism; Oct2016, Vol. 29 Issue 10, p1207-1213, 7p
- Publication Year :
- 2016
-
Abstract
- Primary hyperparathyroidism, typically a disease of the middle aged and the old, is less commonly seen in children. In children the disease has a bimodal age distribution with calcium sensing receptor mutation presenting in infancy as hypercalcemic crises and parathyroid adenoma or hyperplasia presenting later in childhood with bone disease. The childhood parathyroid adenomas are often familial with multiglandular disease and manifest with severe bone disease unlike adults. We report a series of four male patients with juvenile primary hyperparathyroidism, three of whom presented with bone disease masquerading as rickets-osteomalacia. One patient had asymptomatic hypercalcemia with short stature. Parathyroid adenoma was detected in all the four cases and all of them underwent resection of parathyroid adenomas confirmed on histopathology. Post-surgery all the cases had initial hypocalcaemia followed by normocalcemia. One case developed pancreatitis after surgery even after achieving normocalcemia. We conclude that parathyroid adenomas, although uncommon in children, are an important cause of skeletal disease that may initially be confused with hypovitaminosis D. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 0334018X
- Volume :
- 29
- Issue :
- 10
- Database :
- Supplemental Index
- Journal :
- Journal of Pediatric Endocrinology & Metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 118665827
- Full Text :
- https://doi.org/10.1515/jpem-2016-0018