Resection of a large ectopic parathyroid adenoma: A case report. (2016)

• Record Type: Journal Article
• Authors: Sato, Seijiro; Kitahara, Akihiko; Koike, Terumoto; Hashimoto, Takehisa; Ohashi, Riuko; Motoi, Noriko; Tsuchida, Masanori
• Is Part Of: International journal of surgery case reports. Volume 23(2016)
• Page Start: 8
• Page End: 11
• Publication Date: 2016
• Subjects: Hyperparathyroidism -- Parathyroid adenoma -- Ectopic parathyroid tumor -- Osteitis fibrosa cystica; Surgery -- Periodicals; Surgical Procedures, Operative -- Periodicals; Surgery; Electronic journals; Periodicals; 617.005
• DOI: 10.1016/j.ijscr.2016.04.007
• Languages: English
• ISSNs: 2210-2612

Abstract

Highlights: We treated a patient with primary hyperparathyroidism caused by parathyroid adenoma. Parathyroid carcinomas are rare malignant cases of primary hyperparathyroidism. The case of a large parathyroid adenoma with osteitis fibrosa cystica is rare. Differentiation of benign and malignant parathyroid tumors is sometimes difficult. Abstract: Introduction: Parathyroid adenomas are the most common cause of primary hyperparathyroidism. However, cases of parathyroid adenomas greater than 4 cm with osteitis fibrosa cystica are extremely rare. Herein, we report a case of resection of a large ectopic mediastinal parathyroid adenoma. Case presentations: A 46-year-old female with chief complaints of bone pain and gait disturbance was referred to our hospital. Physical examination revealed many mobile teeth in her oral cavity, distortion of the vertebral body, and bowlegs. Laboratory tests showed hypercalcemia, hypophosphatemia, and elevated serum levels of intact parathyroid hormone. Chest CT revealed a 42-mm well–defined, enhancing mass in front of the left-sided tracheal bifurcation. Her findings were diagnosed as primary hyperparathyroidism due to an ectopic mediastinal parathyroid tumor. We performed a median sternotomy and resected the tumor. The tumor was a solid, yellowish-brown mass measuring 42 × 42 mm. Pathologically, the tumor consisted mainly of chief cells with some oxyphil cells; there were no necrotic areas or nuclear atypia, and few mitotic figures. We diagnosed the tumor as an ectopic mediastinal parathyroid adenoma. Eight months after the resection, her serum calcium, phosphorus, and intact PTH levels were normal. Discussion and conclusions: Parathyroid adenomas and parathyroid carcinomas have disparate natural histories, but they can be difficult to differentiate on the basis of preoperative clinical characteristics. We believe that long-term follow-up of these cases is required because there have been few reports on the postoperative natural history of large parathyroid adenomas.