ArticleCase reports in otolaryngology2013
Myoepithelioma of the soft palate: a case report.
Article in Case reports in otolaryngology, 2013. 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.
- MRI and CT features of head and neck myoepithelioma: comparison with parotid pleomorphic adenoma.Japanese journal of radiology · 2026Article
- Decoding myoepithelioma: Highlighting diagnostic dilemmas through a series of rare cases.Journal of oral and maxillofacial pathology : JOMFP · 2025Article
- A Rare Case Presentation of Intraoral Palatal Myoepithelioma.Reports (MDPI) · 2025Article
- Myoepithelioma of the upper lip: A rare case report with a literature review of diagnostic approaches.SAGE open medical case reports · 2025Article
- Article
- Myoepithelioma of the Parotid Gland: A Case Report with Review of the Literature and Classic Histopathology.Case reports in otolaryngology · 2017Article
- Voluminous Myoepithelioma of the Minor Salivary Glands Involving the Base of the Tongue.Case reports in otolaryngology · 2016Article
- Plasmacytoid Myoepithelioma of the Hard Palate in a Child - A Rare Case Report.Journal of clinical and diagnostic research : JCDR · 2015Article
- Clear cell myoepithelioma of palate: A rare case report with brief review of literature.Journal of oral and maxillofacial pathology : JOMFPArticle
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myoepitheliomas are rare benign tumors of myoepithelial cell origin, most commonly seen in parotid gland. These tumors are also reported in oral cavity, soft palate being the most common site of involvement. Imaging findings are nonspecific, and histopathology is necessary to differentiate from other tumors. Our case showed mildly enhancing well-circumscribed mass in soft palate with histological findings consistent with myoepithelioma. The aim of this case report is to increase the awareness about this rare benign tumor regarding its morphological, histopathological, and radiological features along with its possible differential diagnosis.
Identifiers
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Registered trials
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