Fregnani Eduardo-Rodrigues, Leite Amanda-Almeida, Parahyba Claudia-Joffily, Nesrallah Ana-Cristina-Alo, Ramos-Perez Flávia-Maria-de Moraes, Perez Danyel-Elias-da Cruz
Department of Oral Medicine, Hospital Sírio-Libanês, São Paulo, Brazil.
Department of Clinical and Preventive Dentistry, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil.
J Clin Exp Dent. 2016 Oct 1;8(4):e465-e468. doi: 10.4317/jced.52832. eCollection 2016 Oct.
The occurrence of a mandibular lesion as the first sign of multiple myeloma (MM) is uncommon. This report describes a case of MM diagnosed because of a mandibular lesion. A 62-year-old woman presented a destructive radiolucent lesion in the right mandibular ramus. The lesion caused rupture of the anterior cortical bone and extended from the retromolar area to the coronoid process. An incisional biopsy was performed. Histopathological examination revealed numerous pleomorphic plasma cells, some with binucleated nuclei. The tumor cells showed kappa light-chain restriction. Bone marrow biopsy showed findings of massive infiltration of neoplastic plasma cells, besides lesions in the vertebrae. The diagnosis of MM was established. The patient underwent autologous hematopoietic stem-cell transplantation. Currently, the patient is under regular follow up after 40 months of initial treatment. In conclusion, MM should be considered in the differential diagnosis of destructive mandibular lesions. Mandible, multiple myeloma, radiolucent lesion.
下颌骨病变作为多发性骨髓瘤(MM)的首发症状并不常见。本报告描述了一例因下颌骨病变而确诊的MM病例。一名62岁女性右侧下颌支出现一个破坏性的透射性病变。该病变导致前皮质骨破裂,范围从磨牙后区延伸至冠突。进行了切开活检。组织病理学检查发现大量多形性浆细胞,部分为双核。肿瘤细胞显示κ轻链限制。骨髓活检除发现椎体病变外,还显示有肿瘤性浆细胞大量浸润。确诊为MM。患者接受了自体造血干细胞移植。目前,患者在初始治疗40个月后接受定期随访。总之,在鉴别诊断破坏性下颌骨病变时应考虑MM。下颌骨、多发性骨髓瘤、透射性病变。