Ramdurg Praveenkumar, Puranik Surekha R, Dantu Ragunath, Shivanand Rudrayya
1Department of Oral Medicine and Radiology, P.M.N.M Dental College and Hospital, Bagalkot, Karnataka India.
2Deparment of Oral Pathology, P.M.N.M Dental College and Hospital, Bagalkot, Karnataka India.
Indian J Otolaryngol Head Neck Surg. 2019 Oct;71(Suppl 1):38-41. doi: 10.1007/s12070-016-0974-4. Epub 2016 Mar 21.
The solitary neurofibroma is a benign tumor of neuronal origin uncommonly reported in the oral cavity. The possible association of this neoplasia with systemic pathologies, such as von Recklinghausen's disease and multiple endocrine neoplasia, makes its diagnosis fundamental. Solitary isolated neurofibroma of the soft palate not associated with von Recklinghausen's disease is an unusual tumor and probably only four cases have been reported in English literature previously. To the best of our knowledge, our case of soft palate neurofibroma in 17-year-old male represents the fifth reported in English literature, for which complete surgical excision was achieved with uneventful healing.
孤立性神经纤维瘤是一种起源于神经元的良性肿瘤,在口腔中鲜有报道。这种肿瘤可能与系统性疾病相关,如冯雷克林霍增氏病和多发性内分泌肿瘤,因此其诊断至关重要。不伴有冯雷克林霍增氏病的软腭孤立性神经纤维瘤是一种罕见肿瘤,此前英文文献中可能仅报道过4例。据我们所知,我们报道的17岁男性软腭神经纤维瘤病例是英文文献中报道的第5例,该病例通过完整手术切除,愈合顺利。