Is the ghost of brown tumor back again? Features of hypercalcaemic primary hyperparathyroidism we must not forget

Abstract

Two patients presenting with mandible-jaw neoformations were referred to us for endocrine evaluation. A 51-year-old male presented with painful T9 vertebral fracture and multiple osteolytic areas in spine, pelvis, and right mandible branch (Fig. 1A). Metastatic disease was excluded with 18 fluorine-fluorodeoxyglucose positron emission tomography (F-FDG-PET) showing multiple uptakes corresponding to osteolytic areas. Mandible lesion biopsy was not conclusive. Biochemical workup was consistent with hypercalcaemic primary hyperparathyroidism (HPH) (calcium 13.4 mg/dl, range: 8.5–10.5 mg/dl; PTH 667 pg/ml, range 12–88 pg/ml) and vitamin D deficiency (7.8 ng/ml). Neck ultrasound (US) performed at our Unit showed a hypoechoic area under the left thyroid lobe suspected for enlarged parathyroid. This lesion was also identified after CT images re-evaluation (Fig. 1B). Pathology review of the previously provided sample integrated with clinical and radiological information was finally concordant with brown tumor (BT) of the jaw. Spine magnetic resonance was performed and confirmed multiple osteolytic spine lesions typical of BT (Fig. 1C). Left inferior parathyroidectomy was performed and histology showed a parathyroid adenoma. After surgery, serum calcium levels rapidly dropped. High-dose oral and parenteral calcium supplementation as well as vitamin D active metabolite administration was needed in order to contrast hungry bone syndrome development. Concerning vertebral fractures, a corset was applied for at least 1 month and therapy with cholecalciferol was subsequently started. In addition, further treatment with zoledronic acid (5 mg) was administered in order to prevent further fractures. The second case was a 68-year-old woman complaining of mildly painful swelling in the left maxillary branch. Dental CT showed a hypodense lesion at 25, 26, and 27 alveolar regions and small collateral calcifications in the right pharyngeal wall (Fig. 1D). Lesion biopsy was concordant with a giant cell granuloma. Afterwards, biochemical workup showed severe HPH (calcium 15 mg/dl; PTH 898 pg/ml) and vitamin D deficiency (9.8 mg/dl). Neck US performed at our Unit highlighted a hypoechoic and hypervascularized nodule highly suspected for an enlarged left parathyroid (Fig. 1E), then confirmed by scintigraphy (Fig. 1F). Zoledronic acid was started at 4 mg iv, followed by left inferior parathyroidectomy. Histology confirmed a parathyroid adenoma. After surgery, normal calcium levels were obtained by only oral calcium calcitriol and cholecalciferol supplementation. Maxillary swelling progressively decreased, suggesting that the initial histological diagnosis of giant cell granuloma was wrong. Available HPH guidelines do not provide clear indications concerning BT presentation and management [1]. BT appears as a unior multi-lobular osteolytic area with soapbubbling features on X-rays. On CT images, BT looks as a well-defined osteolytic area, with possible fluid signal, rarely showing soft tissue invasion. BT radiological differential diagnosis could be difficult, especially with bone metastases [2]. BT histological diagnosis needs to be integrated with radiological, biochemical, and clinical findings to get the correct diagnosis and avoid expensive secondlevel imaging, such as F-FDG-PET. These two clinical cases underline the importance of evaluating calcium homeostasis in patients presenting with osteolytic facial bone mass suspected for BT. Once HPH is biochemically detected, US is very useful to identify neck masses consistent with enlarged parathyroids that could be confirmed * Maria Chiara Zatelli [email protected]