Shahani Hiba Arshad, Ali Masab, Babar Ilsa, Javeriya Sana, Ahmad Muhammad Husnain, Saeed Humza, Ahmad Uswa, Sehbai Aasim
Department of Internal Medicine, Rawalpindi Medical University, Rawalpindi, Pakistan.
Department of Internal Medicine, Punjab Medical College, Faisalabad, Punjab, Pakistan.
Ann Med Surg (Lond). 2025 Feb 27;87(3):1746-1749. doi: 10.1097/MS9.0000000000003063. eCollection 2025 Mar.
Merkel cell carcinoma (MCC) is a rare but aggressive neuroendocrine skin cancer with a high risk of recurrence and metastasis. It typically affects sun-exposed areas in elderly or immunocompromised individuals. Early diagnosis and management are essential due to its rapid progression and potential for early metastasis.
We report the case of a 65-year-old male with a history of diabetes mellitus and basal cell carcinoma who developed MCC on his left upper extremity. Initial imaging, including a sentinel lymph node biopsy (SLNB) and magnetic resonance imaging (MRI), localized the tumor and assessed lymph node involvement. The SLNB was negative for metastasis, and a wide excision confirmed no residual MCC. Further imaging with positron emission tomography (PET) and computed tomography (CT) scans showed no distant metastasis, indicating localized disease. The patient underwent wide excision followed by radiation therapy (RT) (50 Gy in 25 fractions), experiencing mild post-radiation effects such as swelling and erythema.
MCC poses significant diagnostic and therapeutic challenges due to its nonspecific presentation and rapid progression. In this case, early detection and appropriate imaging allowed for timely intervention. Negative SLNB results and localized disease justified the use of wide excision and MC. Multimodal treatment, including surgery and radiation, is crucial in managing localized MCC.
This case emphasizes the importance of early detection, comprehensive imaging, and multimodal therapy in the management of MCC. Close follow-up remains essential, especially in cases with negative SLNB, to monitor for recurrence or metastasis.
默克尔细胞癌(MCC)是一种罕见但侵袭性强的神经内分泌皮肤癌,复发和转移风险高。它通常影响老年人或免疫功能低下者的阳光暴露部位。由于其进展迅速且有早期转移的可能,早期诊断和治疗至关重要。
我们报告一例65岁男性,有糖尿病和基底细胞癌病史,其左上肢发生了MCC。初始影像学检查,包括前哨淋巴结活检(SLNB)和磁共振成像(MRI),对肿瘤进行了定位并评估了淋巴结受累情况。SLNB转移结果为阴性,广泛切除证实无残留MCC。正电子发射断层扫描(PET)和计算机断层扫描(CT)进一步检查显示无远处转移,表明为局限性疾病。患者接受了广泛切除,随后进行放射治疗(RT)(25次分割,共50 Gy),出现了如肿胀和红斑等轻度放疗后反应。
MCC因其表现不具特异性且进展迅速,带来了重大的诊断和治疗挑战。在本病例中,早期检测和适当的影像学检查使得能够及时进行干预。SLNB结果为阴性且疾病局限,证明了广泛切除和放疗的合理性。包括手术和放疗在内的多模式治疗对于局限性MCC的管理至关重要。
本病例强调了早期检测、全面影像学检查和多模式治疗在MCC管理中的重要性。密切随访仍然至关重要,尤其是在前哨淋巴结活检阴性的病例中,以监测复发或转移情况。