ArticleBMC oral health2019
Solitary neurofibroma of the floor of the mouth: rare localization at lingual nerve with intraoral excision.
Article in BMC oral health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 26 citations in OpenAlex.
- Excision of a Solitary Neurofibroma in the Right Masseter Muscle via a High Perimandibular Approach: A Case Report and Review of the Literature.Case reports in dentistry · 2025Article
- Article
- Solitary intraosseous neurofibroma of the oral cavity: rare localization in the maxilla.BMC oral health · 2024Article
- Beyond Excision: Cryotherapy as a Non-surgical Treatment for Palatal Solitary Neurofibroma.Cureus · 2024Article
- Solitary Neurofibroma of the Maxillary Soft Tissue Causing Bone Destruction: A Rare Presentation.Cureus · 2023Article
- A case of multiple solitary neurofibromas located in the hypopharynx and cervical esophagus.DEN open · 2023Article
- Solitary Neurofibroma of the Hard Palate: A Case Report and Literature Review.The American journal of case reports · 2021Review
- Unusual presentation of submandibular lingual nerve sheath tumour as sublingual stone.BMJ case reports · 2020Article
- Solitary Neurofibroma over Lower Lip: A Rare Manifestation.Journal of cutaneous and aesthetic surgeryArticle
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Authors and funding
4 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundNeurofibromas (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.
conclusionThe 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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