Abuharb Abdullah Ibrahim Ali, Alzamil Abdullah Fahad, Alqarni Khalid Saad, Alsudays Ali M, Alqahtani Saeed M, Alahmadi Rawan Mosleh, Mutairy Alyaa Shojaa Al, Alghamdi Fareed Ramzi
Department of Otorhinolaryngology/Head and Neck Surgery, Imam Mohammed ibn Saud Islamic University, Riyadh 11564, Saudi Arabia.
Department of Otorhinolaryngology/Head and Neck Surgery, Prince Sultan Military Medical City, Riyadh 11564, Saudi Arabia.
World J Clin Cases. 2025 Aug 26;13(24):105244. doi: 10.12998/wjcc.v13.i24.105244.
Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer with high incidence in older and immunocompromised patients. Its occurrence in the nasal dorsum is extremely rare and poses significant diagnostic and therapeutic challenges.
We report the case of a 65-year-old woman with diabetes mellitus and hypertension who presented with a dorsal nasal mass. The initial differential diagnosis favored hemangioma-based clinical examination on imaging. Histopathological examination after excision revealed MCC, necessitating a complex management strategy. A 3 cm × 2 cm nasal mass, initially suspected to be a hemangioma, was excised but revealed MCC with positive margins. Positron emission tomography-computed tomography confirmed metastatic cervical lymphadenopathy. The patient underwent bilateral neck dissection, revealing metastases in seven nodes. Residual activity was treated with radiation therapy, leading to a favorable response after 6 months.
This case highlights the importance of considering MCC in the differential diagnosis of nasal masses, and integrated management.
默克尔细胞癌(MCC)是一种罕见的侵袭性皮肤癌,在老年和免疫功能低下患者中发病率较高。其发生于鼻背部极为罕见,带来了重大的诊断和治疗挑战。
我们报告了一例65岁患有糖尿病和高血压的女性,其鼻背部出现肿物。基于影像学的临床检查,初步鉴别诊断倾向于血管瘤。切除术后的组织病理学检查显示为MCC,需要采取复杂的管理策略。一个最初怀疑为血管瘤的3 cm×2 cm鼻肿物被切除,但显示切缘阳性的MCC。正电子发射断层扫描-计算机断层扫描证实有颈部转移性淋巴结病。患者接受了双侧颈部清扫术,发现7个淋巴结有转移。残余病灶采用放射治疗,6个月后取得了良好的反应。
本病例强调了在鼻肿物的鉴别诊断中考虑MCC以及综合管理的重要性。