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

被引:13
|
作者
Broly, Elyette [1 ,2 ]
Lefevre, Benoit [1 ,2 ,5 ]
Zachar, Dominique [3 ]
Hafian, Hilal [1 ,2 ,4 ,5 ]
机构
[1] Univ Reims, Fac Odontol, Reims, France
[2] Ctr Hosp Univ, Pole Med Buccodent, Hop Maison Blanche, Reims, France
[3] Ctr Hosp Univ, Pole Biol Med & Pathol, Hop Robert Debre, Reims, France
[4] Univ Reims, Lab Rech Nanosci LRN, EA 4682, Reims, France
[5] Univ Reims, Univ Hosp Reims, Maison Blanche Hosp, Dept Oral Med & Oral Surg, 45 Rue Cognac Jay, F-51100 Reims, France
关键词
Solitary neurofibroma; Lingual nerve; Magnetic resonance imaging; S-100; protein; EMA; ORAL-CAVITY; TUMORS; HEAD;
D O I
10.1186/s12903-019-0888-0
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
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.
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页数:8
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