ArticleCureus2025
Primary Malignant Melanoma of the Oropharynx: A Rare Case of a Tonsillar Melanotic Lesion.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- [Tonsillar malignant melanoma presenting as sore throat and tonsillar mass: a case report and literature review].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2026Review
- Case Report: Melanoma of the hard palate presenting initially with gastrointestinal symptoms: the diagnostic pivotal role ofFrontiers in medicine · 2026Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oral malignant melanoma (OMM) is a rare and aggressive malignancy arising from melanocytes in the oral mucosa. We present the case of a 33-year-old Ethiopian female who arrived at the ED with hematemesis, active oral bleeding, and a sensation of suffocation. On examination, a darkly pigmented, ulcerated mass was identified arising from the left posterior tonsillar pillar. Emergency surgery was performed to control the bleeding, and subsequent histopathological analysis confirmed a diagnosis of amelanotic malignant melanoma, supported by immunohistochemical positivity for S100, HMB45, Melan-A, and P16. Advanced imaging with PET-CT and MRI demonstrated a localized tumor without evidence of lymph node involvement or distant metastasis. The patient was treated with neoadjuvant immunotherapy using pembrolizumab, followed by curative-intent radiation therapy targeting high-risk mucosal regions and bilateral cervical nodes. She tolerated the treatment well, though she experienced radiation-induced mucositis, dermatitis, and weight loss. Immunotherapy was resumed post-radiation, and the patient has since completed ten cycles without significant immune-related adverse events. The rarity of OMM and its aggressive clinical behavior underscore the need for heightened clinical suspicion for pigmented or ulcerated oral lesions. This case illustrates the diagnostic and therapeutic complexities of primary oropharyngeal melanoma, especially in the context of amelanotic presentation. It emphasizes the importance of prompt multidisciplinary evaluation, integration of advanced imaging modalities, immunohistochemical profiling, and emerging immunotherapeutic strategies to improve patient outcomes.
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Registered trials
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