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Lymphomas represent the second most common malignancy of the head and neck, with Waldeyer’s ring being the predominant extranodal site. Mantle cell lymphoma (MCL) is an uncommon subtype of non-Hodgkin lymphoma and rarely presents in the lingual tonsil. Only a few such cases have been reported in the literature. We report the case of a 77-year-old woman who presented with a 3-week history of dysphagia and ipsilateral aural fullness. Clinical examination was largely unremarkable except for a multinodular thyroid gland. Fiberoptic laryngoscopy and subsequent CT imaging revealed a 3.8 cm exophytic mass arising from the lingual tonsil, accompanied by bilateral cervical lymphadenopathies. Surgical excision of the lesion yielded a diagnosis of MCL based on immunohistochemical analysis. Staging investigations demonstrated no bone marrow involvement but multiple hypermetabolic cervical lymph nodes; the disease was classified as stage IIA. The patient received 8 cycles of R-CHOP chemoimmunotherapy followed by rituximab maintenance therapy. Post-treatment PET imaging showed complete remission, and the patient remains disease-free 3 years after completion of R-CHOP. Mantle cell lymphoma of the lingual tonsil is exceedingly rare, with only 4 previously reported cases. This case underscores the importance of considering lymphoma in the differential diagnosis of base-of-tongue masses and highlights that multimodal management with chemoimmunotherapy can achieve favorable outcomes, even in elderly patients with limited-stage disease.
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Veken et al. (2026) studied this question.
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