Background: Mucoepidermoid carcinoma originates from reserve cells present in ducts of salivary glands and is the most common malignancy of the salivary glands. It is commonly found in the parotid gland, followed by the palatal and buccal mucous membranes. However, mucoepidermoid carcinoma occurrence in other intraoral sites, including the tongue base, is extremely rare.
Case Presentation: A 33-year-old Chinese man presented with a progressively enlarging mass at the base of his left tongue. Contrast-enhanced computed tomography and magnetic resonance imaging revealed an augmented soft tissue mass in the left jaw region with indistinct boundaries, enlargement of cervical lymph node of uncertain etiology, and no evidence of distant metastasis. A transoral needle biopsy from the mass pathologically revealed low-grade mucoepidermoid carcinoma. Complete transoral excision and cervical lymph node dissection were performed, followed by reconstruction with an anterolateral thigh free flap. Examination of the obtained surgical specimen confirmed low-grade mucoepidermoid carcinoma with MAML2 gene fusion in the base of the tongue. The tumor was removed with negative margins, and the cervical lymph nodes were free of disease. The patient had an uneventful recovery and showed no evidence of recurrence or metastasis at 40 months of follow-up.
Conclusion: We present a rare case of mucoepidermoid carcinoma at the base of the tongue. Furthermore, we review related literature and discuss its clinical features, histopathological characteristics, and treatment strategies.
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http://dx.doi.org/10.1186/s13256-025-05099-0 | DOI Listing |
Indian J Otolaryngol Head Neck Surg
February 2025
Department of ENT, Command Hospital- Eastern Command, Kolkata, India.
Unlabelled: Sino-nasal malignancies are extremely rare accounting < 1% of all malignancies and < 3% of aero-digestive tract tumors. Their surgical pathology is extremely challenging due to the enormous heterogeneity. Few of these sino-nasal tumors may possibly present histologically as clear cell neoplasm.
View Article and Find Full Text PDFDiagn Cytopathol
April 2025
Department of Pediatric Oncology, Institut Curie, Paris cedex, France.
Keratocystoma is a rare benign salivary gland tumor described in 1999. Only 14 cases have been reported in the histopathological literature, with three of them having had a preoperative fine needle aspiration (FNA) performed. All cytological diagnoses were not specific.
View Article and Find Full Text PDFOral Oncol
February 2025
Department of Pathology, School of Medical Sciences, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil. Electronic address:
A 62-year-old male was referred for management of oral squamous cell carcinoma (OSCC), previously diagnosed in another service. The patient complained of persistent oral discomfort for 10 months, reported being a social drinker, and denied smoking. Intraoral examination revealed a vegetating, hardened lesion, measuring 3.
View Article and Find Full Text PDFJ Med Case Rep
February 2025
Department of Pathology, West China Hospital of Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China.
Background: Sclerosing mucoepidermoid carcinoma of the thyroid with eosinophilia (SMECE) is a rare thyroid tumor. More and more reports have proposed that sclerosing mucoepidermoid carcinoma of the thyroid with eosinophilia is significantly invasive, but its origin and pathogenesis are currently controversial.
Case Presentation: We presented a 42-year-old female of Han ethnicity.
Ear Nose Throat J
February 2025
Department of Otolaryngology-Head and Neck Surgery, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Salivary gland cancer (SGC) comprises a very heterogeneous group of rare neoplasms, accounting for approximately 2% to 6% of head and neck malignancies. Surgery with or without adjuvant radiotherapy is the main treatment regimen. However, patients who are ineligible for surgery, including late-stage, recurrent, or metastatic disease, have very limited options.
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