Valentini Filippo, Messineo Daniela, Riminucci Mara, Corsi Alessandro, De Virgilio Armando
Department of Sense Organs, Sapienza University of Rome, Rome, Italy.
Department of Radiologic, Oncologic and Anatomo-Pathologic Sciences, Sapienza University of Rome, Rome, Italy.
Front Oncol. 2025 Jun 10;15:1560133. doi: 10.3389/fonc.2025.1560133. eCollection 2025.
Lymphoepithelial carcinoma (LEC) is a rare malignancy within the head and neck region, histologically akin to undifferentiated nasopharyngeal carcinoma. It is uncommon outside the nasopharynx, particularly in the oropharynx and salivary glands. Granular cell tumors (GCTs), or Abrikossoff's tumors, are rare mesenchymal neoplasms of neural origin, frequently benign but with the potential for malignant transformation. This case report presents an unprecedented clinical scenario of a 62-year-old female patient diagnosed with an HPV/EBV-negative LEC of the right palatine tonsil, coupled with metachronous squamous dysplasia and a contralateral GCT of the true vocal cord. Following initial presentation with cervical swelling, hoarseness, and dysphagia, diagnostic imaging and histopathological analyses confirmed the distinct co-occurrence of these rare entities. The patient underwent multidisciplinary treatment, including transoral robotic surgery (TORS), radical neck dissection, and adjuvant chemoradiotherapy for LEC. Simultaneously, the GCT was managed surgically with close-margin excision, with ongoing surveillance for recurrence. A comprehensive treatment strategy meticulously addressed the unique pathological and therapeutic challenges posed by the simultaneous management of these neoplasms. This case underscores the critical importance of thorough diagnostic evaluation and multidisciplinary planning in managing complex oncological scenarios. The concurrent presentation of LEC and GCT in the head and neck region necessitates individualized approaches, integrating surgical precision and adjuvant therapies. The rarity of this co-occurrence highlights the need for further studies to refine diagnostic markers and therapeutic guidelines, improving patient outcomes.
淋巴上皮癌(LEC)是头颈部区域一种罕见的恶性肿瘤,组织学上类似于未分化鼻咽癌。它在鼻咽部以外并不常见,尤其是在口咽和唾液腺。颗粒细胞瘤(GCTs),即阿布里科索夫瘤,是一种罕见的神经源性间叶肿瘤,通常为良性,但有恶变的可能。本病例报告呈现了一个前所未有的临床病例,一名62岁女性患者被诊断为右侧腭扁桃体HPV/EBV阴性的LEC,同时伴有异时性鳞状上皮发育异常和对侧真声带的GCT。在最初出现颈部肿胀、声音嘶哑和吞咽困难后,诊断性影像学检查和组织病理学分析证实了这些罕见实体的明显同时存在。患者接受了多学科治疗,包括经口机器人手术(TORS)、根治性颈清扫术以及针对LEC的辅助放化疗。同时,GCT通过手术进行切缘阴性切除处理,并持续监测复发情况。一个全面的治疗策略精心应对了同时处理这些肿瘤所带来的独特病理和治疗挑战。本病例强调了在处理复杂肿瘤病例时进行全面诊断评估和多学科规划的至关重要性。头颈部区域LEC和GCT的同时出现需要个体化方法,整合手术精准性和辅助治疗。这种同时出现的罕见性凸显了进一步研究以完善诊断标志物和治疗指南、改善患者预后的必要性。