Albaldawy Mazin J, Ebaied Tamer, Al Shamsi Humaid O, Alkinain Ashraf, Faruk Abbu Rahil U
Department of Oncology, Al Dhannah Hospital, Abu Dhabi, ARE.
Department of Ear, Nose, and Throat, Al Dhannah Hospital, Abu Dhabi, ARE.
Cureus. 2025 Apr 20;17(4):e82637. doi: 10.7759/cureus.82637. eCollection 2025 Apr.
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.
口腔恶性黑色素瘤(OMM)是一种罕见且侵袭性强的恶性肿瘤,起源于口腔黏膜中的黑素细胞。我们报告了一例33岁的埃塞俄比亚女性病例,该患者因呕血、口腔活动性出血和窒息感而被送往急诊科。检查时,发现左侧扁桃体后柱有一个色素沉着、溃疡的肿块。进行了急诊手术以控制出血,随后的组织病理学分析证实为无色素性恶性黑色素瘤,S100、HMB45、Melan-A和P16免疫组化呈阳性支持该诊断。PET-CT和MRI的高级影像学检查显示为局限性肿瘤,无淋巴结受累或远处转移的证据。患者接受了帕博利珠单抗新辅助免疫治疗,随后针对高危黏膜区域和双侧颈部淋巴结进行了根治性放疗。她对治疗耐受性良好,尽管出现了放射性粘膜炎、皮炎和体重减轻。放疗后恢复免疫治疗,此后患者已完成十个周期,无明显的免疫相关不良事件。OMM的罕见性及其侵袭性临床行为强调了对色素沉着或溃疡性口腔病变提高临床怀疑的必要性。该病例说明了原发性口咽黑色素瘤的诊断和治疗复杂性,尤其是在无色素表现的情况下。它强调了及时进行多学科评估、整合先进影像学检查、免疫组化分析和新兴免疫治疗策略以改善患者预后的重要性。