Altamirano De La Cruz Azalea Guadalupe, Orozco Velazco Christian Daniel, Ramírez Saavedra Abraham, Salazar López Maria Daniela, Cruz Dominguez Karen Sofia
Internal Medicine, Mexican Social Security Institute (IMSS) General Zone Hospital No. 8, Ensenada, MEX.
Internal Medicine, Hospital Angeles Metropolitano, Mexico City, MEX.
Cureus. 2025 Aug 16;17(8):e90232. doi: 10.7759/cureus.90232. eCollection 2025 Aug.
Merkel cell carcinoma (MCC) is a rare but exceptionally aggressive neuroendocrine skin cancer, characterized by low global incidence yet significant clinical impact due to its propensity for early metastasis. Regional lymph node metastases occur frequently, while distant metastases are present in a substantial proportion of patients. The rising incidence over recent decades is largely attributed to the aging global population, associated immunosenescence, and increased cumulative ultraviolet (UV) radiation exposure, particularly UVB radiation. MCC's medical significance lies in its rapid progression, high metastatic potential, and poor prognosis, with survival rates decreasing markedly from localized disease to cases with regional lymph node involvement. This underscores the need for prompt recognition and management to optimize patient outcomes. Key risk factors include advanced age, with an exponential increase in incidence after retirement age, immunosuppression, and chronic sun/UV exposure. Merkel cell polyomavirus has been identified as an important etiologic factor in the majority of cases. This case report describes an elderly female patient who presented with a rapidly growing, ulcerated cervical lesion that had progressed substantially over several months. The lesion was initially misdiagnosed and inadequately treated with minor excision without histopathological analysis. Subsequent rapid local recurrence, extensive regional lymph node involvement, and definitive diagnosis, confirmed by characteristic immunohistochemical staining patterns, highlight the critical need for high clinical suspicion and meticulous histopathological evaluation. Palliative radiotherapy provided measurable clinical benefit, including significant pain relief and notable tumor size reduction. This case exemplifies how deficiencies in initial management can dramatically alter disease trajectory in aggressive malignancies, transforming potentially curable early-stage disease into advanced locoregional involvement requiring palliative treatment with markedly reduced survival expectations.
默克尔细胞癌(MCC)是一种罕见但极具侵袭性的神经内分泌皮肤癌,其全球发病率较低,但因其易于早期转移而具有重大临床影响。区域淋巴结转移很常见,而相当一部分患者会出现远处转移。近几十年来发病率上升主要归因于全球人口老龄化、相关的免疫衰老以及累积紫外线(UV)辐射暴露增加,尤其是UVB辐射。MCC的医学意义在于其进展迅速、转移潜力高且预后差,从局限性疾病到区域淋巴结受累病例,生存率显著下降。这凸显了及时识别和管理以优化患者预后的必要性。关键风险因素包括高龄,退休年龄后发病率呈指数级增长、免疫抑制以及长期阳光/紫外线暴露。默克尔细胞多瘤病毒已被确定为大多数病例中的重要病因。本病例报告描述了一名老年女性患者,她出现了一个快速生长、溃疡的颈部病变,在几个月内有显著进展。该病变最初被误诊,仅进行了小范围切除且未进行组织病理学分析,治疗不充分。随后病变迅速局部复发、广泛区域淋巴结受累,通过特征性免疫组化染色模式确诊,突出了高度临床怀疑和细致组织病理学评估的迫切需求。姑息性放疗带来了可测量的临床益处,包括显著缓解疼痛和明显缩小肿瘤大小。该病例例证了初始管理中的缺陷如何能极大地改变侵袭性恶性肿瘤的疾病轨迹,将潜在可治愈的早期疾病转变为需要姑息治疗且生存期望显著降低的晚期局部区域受累疾病。