Can Özgür, Boynueğri Başak, Gökçe Ali Murat, Özdemir Ebru, Ferhatoğlu Ferhat, Canbakan Mustafa, Şahin Gülizar Manga, Titiz Mesut İzzet, Apaydın Süheyla
Departments of Nephrology, Haydarpaşa Numune Training and Research Hospital, Turkey.
Departments of General Surgery and Transplantation, Haydarpaşa Numune Training and Research Hospital, Turkey.
Case Rep Nephrol Dial. 2016 Mar 18;6(1):46-52. doi: 10.1159/000444703. eCollection 2016 Jan-Apr.
Brown tumors are focal bone lesions, encountered in patients with uncontrolled hyperparathyroidism. They can be located in any part of the skeleton. Clinically significant lesions in the craniofacial bones are rare. Craniofacial involvement may cause facial disfiguration and compromise social ease of the patient and normal functions, such as chewing, talking, and breathing. In this case report, we present a patient with a brown tumor of the craniofacial bones provoked by secondary hyperparathyroidism and review the last 10 years of craniofacial brown tumors associated with secondary hyperparathyroidism in the English literature.
棕色瘤是一种局灶性骨病变，见于甲状旁腺功能亢进未得到控制的患者。它们可位于骨骼的任何部位。颅面骨出现具有临床意义的病变较为罕见。颅面骨受累可能导致面部畸形，影响患者的社交舒适度以及咀嚼、说话和呼吸等正常功能。在本病例报告中，我们介绍了一名由继发性甲状旁腺功能亢进引发颅面骨棕色瘤的患者，并回顾了英文文献中过去10年与继发性甲状旁腺功能亢进相关的颅面棕色瘤病例。
