Akhlaghi Fahimeh, Mashhadiabbas Fatemeh, Baseri Milad, Toghchi Sanaz Gholami, Chafjiri Maryam Mohammadalizadeh, Khorsand Ardeshir
Department of Oral and Maxillofacial Surgery, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Oral and Maxillofacial Pathology, Dentistry Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Case Rep Dent. 2025 Apr 2;2025:6778806. doi: 10.1155/crid/6778806. eCollection 2025.
Neurofibroma (NF) is a benign peripheral nerve sheath tumor which consists of Schwann cells, perineurial-like cells, and fibroblasts. The NF can be central or peripheral, alone or multiple which is a manifestation of Type I neurofibromatosis. NFs are mostly found in the tongue, oral mucosa, and lips when appearing in the mouth cavity, but they are rare at palate in a solitary form. We report a case of a solitary NF originating in the hard palate in a 30-year-old woman. The patient had an asymptomatic, nonulcerated, sessile, pink, and smooth nodule measuring 15 × 25 × 5 mm with a firm consistency and defined border on the left side of the posterior part of the hard palate. She had a similar history about 12 years ago which was diagnosed as a benign myxoid tumor which was excised that time. The lesion was excised with a 3-mm safe margin. The periosteum was excised, but the palatal bone was intact and was not excised. IHC was positive for S-100 immunostaining. Eventually, the mass was diagnosed as a NF. The important point is that following the patient with NF is necessary, because it could be the primary sign of Type I neurofibromatosis. The follow-up of this patient is continuing, and until the accomplishment of this report, no relapse was evident.
神经纤维瘤(NF)是一种良性周围神经鞘瘤,由施万细胞、类神经束膜细胞和成纤维细胞组成。NF可以是中枢性或周围性的,单发或多发,是I型神经纤维瘤病的一种表现。NF出现在口腔时,大多见于舌、口腔黏膜和唇部,但孤立形式出现在腭部的情况罕见。我们报告一例30岁女性硬腭起源的孤立性NF病例。患者硬腭后部左侧有一个无症状、无溃疡、无蒂、粉红色、表面光滑的结节,大小为15×25×5毫米,质地硬,边界清晰。她大约12年前有过类似病史,当时被诊断为良性黏液瘤并已切除。病变以3毫米安全切缘切除。骨膜被切除,但腭骨完整未被切除。免疫组化S-100染色呈阳性。最终,肿块被诊断为NF。重要的是,对NF患者进行随访是必要的,因为它可能是I型神经纤维瘤病的主要体征。该患者的随访仍在继续,截至本报告完成时,未见复发迹象。