Lim Daniel, Tan Chuey Chuan, Tilakaratne Wanninayake Mudiyanselage, Goh Yet Ching
University of Malaya, Faculty of Dentistry, Department of Oral and Maxillofacial Clinical Sciences, Malaysia.
University of Malaya, Faculty of Dentistry, Department of Oral and Maxillofacial Clinical Sciences, Malaysia.
Braz J Otorhinolaryngol. 2022 Jan-Feb;88(1):118-129. doi: 10.1016/j.bjorl.2021.01.007. Epub 2021 Feb 27.
Sclerosing odontogenic carcinoma was a new addition to the list of head and neck tumors by World Health Organization in 2017. This lesion has scarcely been reported and a lack of pathognomonic markers for diagnosis exists.
The aim of the study was to summarize findings from the available literature to provide up-to-date information on sclerosing odontogenic carcinoma and to analyse clinical, radiological, and histopathological features to obtain information for and against as an odontogenic malignancy.
We conducted a comprehensive review of literature by searching Pubmed, EBSCO and Web of Science databases, according to PRISMA guidelines. All the cases reported as sclerosing odontogenic carcinoma in English were included. Data retrieved from the articles were gender, age, clinical features, site, relevant medical history, radiographical findings, histopathological findings, immunohistochemical findings, treatments provided and prognosis.
Mean age at diagnosis of sclerosing odontogenic carcinoma was 54.4 years with a very slight female predilection. Sclerosing odontogenic carcinoma was commonly reported in the mandible as an expansile swelling which can be asymptomatic or associated with pain or paraesthesia. They appeared radiolucent with cortical resorption in radiograph evaluation. Histologically, sclerosing odontogenic carcinoma was composed of epithelioid cells in dense, fibrous, or sclerotic stroma with equivocal perineural invasion. Mild cellular atypia and inconspicuous mitotic activity were observed. There is no specific immunohistochemical marker for sclerosing odontogenic carcinoma. AE1/AE3, CK 5/6, CK 14, CK19, p63 and E-cadherin were the widely expressed markers for sclerosing odontogenic carcinoma. Surgical resection was the main treatment provided with no recurrence in most cases. No cases of metastasis were reported.
From the literature available, sclerosing odontogenic carcinoma is justifiable as a malignant tumor with no or unknown metastatic potential which can be adequately treated with surgical resection. However, there is insufficient evidence for histological grading or degree of malignancy of this tumor.
2017年,硬化性牙源性癌被世界卫生组织新增列入头颈部肿瘤名单。该病变鲜有报道,且缺乏诊断的特征性标志物。
本研究旨在总结现有文献的研究结果,提供关于硬化性牙源性癌的最新信息,并分析临床、放射学和组织病理学特征,以获取支持和反对其为牙源性恶性肿瘤的信息。
我们按照PRISMA指南,通过检索PubMed、EBSCO和科学网数据库对文献进行了全面综述。纳入所有以英文报道为硬化性牙源性癌的病例。从文章中检索的数据包括性别、年龄、临床特征、部位、相关病史、放射学表现、组织病理学表现、免疫组化表现、所采取的治疗措施及预后。
硬化性牙源性癌的平均诊断年龄为54.4岁,女性略占优势。硬化性牙源性癌常见于下颌骨,表现为膨胀性肿块,可无症状,或伴有疼痛或感觉异常。在X线片评估中,它们表现为透射影伴皮质吸收。组织学上,硬化性牙源性癌由密集、纤维性或硬化性间质中的上皮样细胞组成,伴有可疑的神经周浸润。观察到轻度细胞异型性和不明显的有丝分裂活性。硬化性牙源性癌没有特异性的免疫组化标志物。AE1/AE3、CK 5/6、CK 14、CK19、p63和E-钙黏蛋白是硬化性牙源性癌广泛表达的标志物。手术切除是主要的治疗方法,大多数病例无复发。未报告转移病例。
从现有文献来看,硬化性牙源性癌作为一种无转移潜能或转移潜能未知的恶性肿瘤是合理的,手术切除可对其进行充分治疗。然而,关于该肿瘤的组织学分级或恶性程度,证据并不充分。