Sideris Giorgos, Gogoulos Panagiotis P, Nastos Theofanis, Damaskou Vasileia, Vlastarakos Petros V
Second ENT Department, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, GRC.
Second Pathology Department, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, GRC.
Cureus. 2025 Jun 17;17(6):e86192. doi: 10.7759/cureus.86192. eCollection 2025 Jun.
Rhabdomyosarcoma (RMS) of the tongue in adults is an exceptionally rare and aggressive malignancy, often posing significant challenges in diagnosis and management. Due to its rarity, most available data come from isolated case reports and small retrospective studies. It typically presents as a rapidly enlarging tongue mass, leading to symptoms such as dysphagia, speech disturbances, and airway obstruction. Diagnosis relies on imaging studies and histopathological confirmation, with immunohistochemical markers playing a crucial role in differentiation from other malignancies. We present a case of an adult patient who developed a tongue mass with progressive symptoms. Imaging revealed a large tumor at the base of the tongue, and biopsy confirmed a high-grade RMS. Due to worsening clinical symptoms, surgical resection was performed before the final histopathological diagnosis was available. Despite initial treatment, the tumor recurred, requiring a second surgical intervention followed by radiation therapy. At the 12-month follow-up, the patient remained disease-free. A literature review identified 12 previously reported cases of adult tongue RMS, highlighting the variability in treatment approaches, with most patients undergoing surgical resection, often combined with chemotherapy or radiotherapy. Given the high risk of recurrence, a multimodal treatment strategy is necessary to improve survival outcomes. Early diagnosis and regular follow-up are critical as recurrence often necessitates additional surgical interventions. Further studies are needed to better understand the long-term prognosis and optimize treatment strategies for this rare malignancy.
成人舌横纹肌肉瘤(RMS)是一种极为罕见且侵袭性强的恶性肿瘤,在诊断和治疗方面常常带来重大挑战。由于其罕见性,大多数现有数据来自孤立的病例报告和小型回顾性研究。它通常表现为迅速增大的舌部肿块,导致吞咽困难、言语障碍和气道阻塞等症状。诊断依赖于影像学检查和组织病理学确认,免疫组化标志物在与其他恶性肿瘤的鉴别中起着关键作用。我们报告一例成年患者,其出现伴有进行性症状的舌部肿块。影像学显示舌根部有一个大肿瘤,活检证实为高级别RMS。由于临床症状恶化,在最终组织病理学诊断出来之前进行了手术切除。尽管进行了初始治疗,肿瘤仍复发,需要进行第二次手术干预,随后进行放射治疗。在12个月的随访中,患者无疾病复发。文献综述确定了12例先前报道的成人舌RMS病例,突出了治疗方法的多样性,大多数患者接受了手术切除,常联合化疗或放疗。鉴于复发风险高,多模式治疗策略对于改善生存结果是必要的。早期诊断和定期随访至关重要,因为复发往往需要额外的手术干预。需要进一步研究以更好地了解这种罕见恶性肿瘤的长期预后并优化治疗策略。