Stoev Lyuben, Yankov Yanko G, Nikolaev Nikolay I, Stoeva Martina
General and Clinical Pathology, Forensic Medicine and Deontology, Medical University of Varna, Varna, BGR.
Maxillofacial Surgery, University Hospital St. Marina, Varna, BGR.
Cureus. 2024 Mar 24;16(3):e56836. doi: 10.7759/cureus.56836. eCollection 2024 Mar.
Schwannomas are not uncommon in the maxillofacial region; however, those with intraoral localization and, in particular, the hard palate are among the least frequently described. In the current case report, we present a 17-year-old girl with a histologically verified schwannoma of the hard palate on the right, originating from the right greater palatine nerve. In her case, despite the lysis of the palatine bone from the tumor compression, the disease is asymptomatic, causing only a weak sensation of local discomfort. The lesion was removed surgically under general anesthesia and the resulting defect of the palatal mucosa was compensated by plastic reconstruction with a lingual mucosal flap on a posterior feeding base. The recovery period was uneventful.
神经鞘瘤在颌面部并不少见;然而,发生于口腔内尤其是硬腭的神经鞘瘤是报道最少的部位之一。在本病例报告中,我们介绍了一名17岁女孩,其右侧硬腭经组织学证实为神经鞘瘤,起源于右侧腭大神经。在她的病例中,尽管肿瘤压迫导致腭骨溶解,但该疾病无症状,仅引起轻微的局部不适感。病变在全身麻醉下手术切除,腭黏膜的缺损通过带蒂舌黏膜瓣的整形重建得以修复。恢复期顺利。