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口腔底部孤立性神经纤维瘤:罕见位于舌神经并经口内切除。

Solitary neurofibroma of the floor of the mouth: rare localization at lingual nerve with intraoral excision.

机构信息

Faculté d'odontologie, Université Reims Champagne Ardenne, Reims, France.

Pôle de Médecine Bucco-Dentaire, Hôpital Maison Blanche, Centre Hospitalier Universitaire, Reims, France.

出版信息

BMC Oral Health. 2019 Aug 29;19(1):197. doi: 10.1186/s12903-019-0888-0.

Abstract

BACKGROUND

Neurofibromas (NF) are benign tumors of the peripheral nerves that are composed of Schwann cells, perineural-like cells and fibroblasts. The differential diagnosis for a solitary intraneural variant of neurofibroma arising in the floor of the mouth is broad and includes a submandibular gland neoplasm and adenopathy, among others. The intraoral approach is the best choice for a medium-sized lesion.

CASE PRESENTATION

We report a rare case of a solitary neurofibroma of the floor of the mouth in a 31-year-old male. The patient consulted the dental emergency department for acute pain of the left mandible. Systematic clinical examination revealed the presence of a mass in the left mouth floor. The panoramic x-ray was not conclusive and the magnetic resonance imaging (MRI) revealed a well-defined soft tissue lesion with homogenous isosignal intensity on the T1-weighted image, high intensity signal on the T2-weighted image and heterogeneous enhancement following contrast-enhancement on the T1-weighted Fast Sat image. The surgical excision of the soft-tissue neoplasm was accomplished by an intraoral approach. The specimen was sent for histopathologic analysis and Immunohistochemical studies which confirmed the diagnosis of a myxoid predominant intraneural solitary neurofibroma.

CONCLUSION

The diagnosis of neurofibroma was confirmed by histopathological evaluation and immunohistochemical studies which also excluded other entities in the histopathologic differential diagnosis including schwannoma and a malignant peripheral nerve sheath tumor among other. Localized (solitary) neurofibromas most often occur as sporadic lesions, however; diagnosis of a solitary neurofibroma prompts clinical evaluation to exclude the remote possibility of neurofibromatosis. The purpose of this case report is to raise awareness of the uncommon presentation of neurofibroma and to document the successful management of such a lesion using an intraoral approach.

摘要

背景

神经纤维瘤(NF)是一种良性的周围神经肿瘤,由施万细胞、类神经周围细胞和纤维母细胞组成。口腔底部单发神经纤维瘤的鉴别诊断范围很广,包括下颌下腺肿瘤和淋巴结病等。对于中等大小的病变,口腔内入路是最佳选择。

病例介绍

我们报告了一例罕见的口腔底部单发神经纤维瘤病例,患者为 31 岁男性。患者因左下颌急性疼痛就诊于牙科急诊。系统临床检查发现左口腔底部有一肿块。全景 X 光片无明确结论,磁共振成像(MRI)显示边界清楚的软组织病变,T1 加权图像呈均匀等信号强度,T2 加权图像呈高信号强度,T1 加权快速 Sat 图像增强后呈不均匀增强。通过口腔内入路切除软组织肿瘤。标本送组织病理学分析和免疫组织化学研究,证实为粘液为主的神经内单发神经纤维瘤。

结论

通过组织病理学评估和免疫组织化学研究诊断为神经纤维瘤,也排除了神经鞘瘤和恶性周围神经鞘肿瘤等其他组织学鉴别诊断中的其他实体。局限性(单发)神经纤维瘤多为散发性病变,但单发神经纤维瘤的诊断提示临床评估以排除神经纤维瘤病的可能性。本病例报告的目的是提高对神经纤维瘤罕见表现的认识,并记录使用口腔内入路成功治疗此类病变的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc90/6714308/77ba7577324e/12903_2019_888_Fig1_HTML.jpg

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