NON-SYNDROMIC SOLITARY NEUROFIBROMA IN FLOOR OF THE MOUTH: A CASE REPORT

N. Balan, M SudhaaMani, S YasmeenAhamed, Sivaraman G.S, Ezhilarasi
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Abstract

Neurofibromas are rare in the head and neck region, but most frequent tumor of neural origin. Oral hard and soft tissue is affected bythe tumor. In this paper, we describe an unusual case of non-syndromic solitary neurofibroma of the floor of the mouth in a 70-yearfemalepatient with a chief complaint of growth in the floor of the mouth for the past 3 months. An occlusal, intraoral periapicalradiograph and CT imaging were done. After confirming the diagnosis, the lesion was excised under local anesthesia and the specimenwas submitted for histopathological examination. On subsequent follow-up, the patient was asymptomatic. Intraoral neurofibromaalthough uncommon, deserve special attention because of their similarity with other inflammatory neoplastic condition, and theirtendency to undergo malignant transformation.
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口腔底无综合征孤立性神经纤维瘤1例报告
神经纤维瘤在头颈部是罕见的,但最常见的肿瘤神经起源。口腔软硬组织受肿瘤影响。在这篇论文中,我们描述了一个不寻常的病例无综合征孤立神经纤维瘤的口腔底部在一个70岁的女性患者的主要投诉在口腔底部的增长在过去的3个月。行咬合、口内根尖周x线片及CT检查。确诊后,局部麻醉下切除病变,标本行组织病理学检查。在随后的随访中,患者无症状。口腔内神经纤维瘤虽然不常见,但由于其与其他炎症性肿瘤的相似性以及其恶性转化的倾向,值得特别关注。
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