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2
Merkel cell carcinoma: a review of clinical management with focus on Asian patients. Merkel 细胞癌:临床管理综述,重点关注亚洲患者。
Jpn J Clin Oncol. 2023 Jul 31;53(8):673-679. doi: 10.1093/jjco/hyad059.
3
Treatment and survival outcomes in metastatic Merkel cell carcinoma: Analysis of 2010 patients from the SEER database.转移性默克尔细胞癌的治疗与生存结局:来自监测、流行病学和最终结果(SEER)数据库的2010例患者分析
Cancer Treat Res Commun. 2022;33:100665. doi: 10.1016/j.ctarc.2022.100665. Epub 2022 Nov 24.
4
Gender and immunosuppression impact on Merkel cell carcinoma diagnosis and prognosis. A population based cohort study.性别和免疫抑制对默克尔细胞癌诊断及预后的影响。一项基于人群的队列研究。
Skin Health Dis. 2021 Dec 8;2(1):e80. doi: 10.1002/ski2.80. eCollection 2022 Mar.
5
Surgical Management of Merkel Cell Carcinoma.默克尔细胞癌的外科治疗。
Otolaryngol Clin North Am. 2021 Apr;54(2):357-368. doi: 10.1016/j.otc.2020.11.008. Epub 2021 Feb 15.
6
How we treat Merkel cell carcinoma: within and beyond current guidelines.我们如何治疗 Merkel 细胞癌:现行指南内及以外的治疗方法。
Future Oncol. 2021 Apr;17(11):1363-1377. doi: 10.2217/fon-2020-1036. Epub 2021 Jan 29.
7
Targeting the epigenetic addiction of Merkel cell carcinoma.针对 Merkel 细胞癌的表观遗传成瘾。
EMBO Mol Med. 2020 Nov 6;12(11):e13347. doi: 10.15252/emmm.202013347. Epub 2020 Oct 16.
8
Diagnostic accuracy of a panel of immunohistochemical and molecular markers to distinguish Merkel cell carcinoma from other neuroendocrine carcinomas.一组免疫组织化学和分子标志物鉴别 Merkel 细胞癌与其他神经内分泌癌的诊断准确性。
Mod Pathol. 2019 Apr;32(4):499-510. doi: 10.1038/s41379-018-0155-y. Epub 2018 Oct 22.
9
Merkel cell carcinoma.默克尔细胞癌。
Nat Rev Dis Primers. 2017 Oct 26;3:17077. doi: 10.1038/nrdp.2017.77.
10
Definitive radiotherapy for Merkel cell carcinoma confers clinically meaningful in-field locoregional control: A review and analysis of the literature.根治性放疗治疗 Merkel 细胞癌可实现有临床意义的瘤内局部区域控制:文献回顾与分析。
J Am Acad Dermatol. 2017 Jul;77(1):142-148.e1. doi: 10.1016/j.jaad.2017.02.015. Epub 2017 May 9.

一名患有基底细胞癌的患者发生默克尔细胞癌:一例前哨淋巴结活检阴性的局限性疾病病例。

Merkel cell carcinoma in a patient with basal cell carcinoma: a case of localized disease with negative sentinel node biopsy.

作者信息

Shahani Hiba Arshad, Ali Masab, Babar Ilsa, Javeriya Sana, Ahmad Muhammad Husnain, Saeed Humza, Ahmad Uswa, Sehbai Aasim

机构信息

Department of Internal Medicine, Rawalpindi Medical University, Rawalpindi, Pakistan.

Department of Internal Medicine, Punjab Medical College, Faisalabad, Punjab, Pakistan.

出版信息

Ann Med Surg (Lond). 2025 Feb 27;87(3):1746-1749. doi: 10.1097/MS9.0000000000003063. eCollection 2025 Mar.

DOI:10.1097/MS9.0000000000003063
PMID:40213245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11981377/
Abstract

INTRODUCTION

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.

CASE PRESENTATION

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.

CLINICAL DISCUSSION

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.

CONCLUSION

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.

摘要

引言

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。

病例介绍

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。

临床讨论

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。

结论

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。