Teixeira Lucas Novaes, da Cruz Eduardo Zambaldi, Rosa Ana Cláudia Garcia, Rodrigues Anderson Abdo, Passador-Santos Fabrício, de Araújo Vera Cavalcanti, Soares Andresa Borges
Faculdade São Leopoldo Mandic, Rua José Rocha Junqueira 13, Swift, 13045-755 Campinas, SP, Brazil.
School of Medicine, Federal University of Tocantins, Avenida NS-15, Quadra 109, Norte, S/n-Plano Diretor Norte, Palmas TO 77001-090, Brazil.
Case Rep Oncol Med. 2021 Nov 28;2021:9945591. doi: 10.1155/2021/9945591. eCollection 2021.
Synovial sarcoma (SS) is a rare malignant mesenchymal tumor that mainly occurs in body extremities, being uncommon in the head and neck region. In the present study, we described a case of primary intraosseous SS arising in the mandible of a 22-year-old young male. The patient reported a painful swelling on the left side of the mandible for the last 7 months. Imaging exams showed the presence of an expansive and multilocular radiolucent lesion, extending from the left condyle to the mandibular body. The clinic diagnostic hypotheses were ameloblastoma or malignant neoplasm. Histologically, the lesion was characterized by a proliferation of spindle cells exhibiting vesicular nuclei and evident nucleolus. Neoplastic cells were positive for AE1/AE3, cytokeratin 7, vimentin, CD-99, and TLE-1 and negative for CD-34, S-100, SMA, and HHF-35. A combination of clinical, histologic, and immunohistochemical characteristics supported the diagnosis of SS. The patient was referred for treatment, and preoperative exams did not reveal any other tumor foci in the body of the patient. The final diagnosis was of a primary intraosseous SS of the mandible.
滑膜肉瘤(SS)是一种罕见的恶性间叶组织肿瘤,主要发生于四肢,在头颈部区域较为少见。在本研究中,我们描述了一例发生于一名22岁年轻男性下颌骨的原发性骨内滑膜肉瘤病例。患者自述在过去7个月里下颌骨左侧出现疼痛性肿胀。影像学检查显示存在一个膨胀性、多房性透光性病变,从左髁突延伸至下颌体。临床诊断假设为成釉细胞瘤或恶性肿瘤。组织学上,病变的特征是梭形细胞增殖,细胞核呈空泡状,核仁明显。肿瘤细胞AE1/AE3、细胞角蛋白7、波形蛋白、CD - 99和TLE - 1呈阳性,而CD - 34、S - 100、平滑肌肌动蛋白(SMA)和HHF - 35呈阴性。临床、组织学和免疫组化特征相结合支持滑膜肉瘤的诊断。患者被转诊接受治疗,术前检查未发现患者体内有任何其他肿瘤病灶。最终诊断为下颌骨原发性骨内滑膜肉瘤。