Brown tumor as an indication of a rare parathyroid carcinoma: A diagnostic challenge
Brown tumor reveals parathyroid carcinoma
Keywords:
Brown tumor, Parathyroid carcinoma, Severe hypercalcemia, osteitis fibrosa cystica, Parathyroidectomy, hungry bone syndromeAbstract
Parathyroid carcinoma is an exceptionally rare cause of primary hyperparathyroidism, comprising less than 1% of cases. Its presentation often overlaps with benign etiologies, thereby posing significant diagnostic challenges. We present a case of a 70-year-old male with a history of prostate cancer who presented with profound hypercalcemia and markedly elevated parathyroid hormone. Imaging revealed lytic rib lesions consistent with osteitis fibrosa cystica (brown tumor). Surgical resection of a parathyroid mass confirmed parathyroid carcinoma. Postoperatively, the patient experienced symptomatic hypocalcemia due to non-adherence with calcium supplementation. This case highlights the need for clinical suspicion of parathyroid carcinoma in cases of severe hypercalcemia and skeletal manifestations and the importance of postoperative management in preventing complications such as hungry bone syndrome.
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Copyright (c) 2026 Noor Riaz, Lexington Lemmon, Hamda Soubagle, Necial Marcelin, Mohammad Masri
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.








