Hypercalcemia in Necrobiotic Xanthogranuloma: First Reported Case and Insight Into Treatment.

Abstract

Necrobiotic xanthogranuloma (NXG) is a rare systemic and progressive granulomatous disease first described in 1980. Given no established first-line therapy, treatment focuses on the control of skin lesions and associated complications. Despite it being a granulomatous disease, NXG has not been associated with hypercalcemia. About 140 cases of NXG have been reported to date but, to our knowledge, this is the first case to be complicated by hypercalcemia. Our case confirms a granulomatous disease-mediated production of 1α-hydroxylase leading to increased synthesis of 1,25-dihydroxyvitamin D and subsequent hypercalcemia. Based on this pathophysiology, we elected to start systemic glucocorticoids, titrated to clinical and metabolic response. Steroid-sparing agents need to be considered to avoid long-term complications but continue controlling this granulomatous disease. © 2017 American Society for Bone and Mineral Research.

• Authors: Jad G Sfeir, Richard J Zogala, Violeta B Popii
• Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (J Bone Miner Res) Vol. 32 Issue 4 Pg. 784-787 (04 2017) ISSN: 1523-4681 [Electronic] United States
• PMID: 27886405 (Publication Type: Case Reports, Journal Article)
• Copyright: © 2016 American Society for Bone and Mineral Research.

Topics

• Aged, 80 and over
• Female
• Fibroblast Growth Factor-23
• Humans
• Hypercalcemia (blood, complications, diagnosis, therapy)
• Necrobiotic Xanthogranuloma (blood, complications, diagnosis, therapy)