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Merkel cell carcinoma in the community setting: a casereport

机译:社区默克尔细胞癌病例报告

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摘要

Merkel cell carcinoma (MCC) is a rare neuroendocrine tumor of the skin initially believed to arise from the Merkel cells. In the community setting a general radiation oncologist may only encounter this pathology in a handful of cases over the course of their career. Due to the low incidence of this malignancy, few prospective randomized controlled trials have ever been conducted and therefore guidelines are based on relatively lower levels of evidence upon which the clinical recommendations are made. We discuss the case of a female in her 90s presenting with a classic MCC primary lesion, as well as satellite lesions proximal to both the primary and the draining regional lymph nodes with no evidence of nodal involvement. Here we discuss the presentation, management, treatment planning, underlying pathology, results and sequelae of treatment. We also review new treatment modalities, and the most current staging systems and guidelines.
机译:默克尔细胞癌(MCC)是一种罕见的皮肤神经内分泌肿瘤,最初被认为是由默克尔细胞引起的。在社区环境中,普通放射肿瘤科医生可能在其职业生涯中只有少数情况下会遇到这种病理情况。由于这种恶性肿瘤的发生率低,因此几乎没有进行过任何前瞻性随机对照试验,因此指南基于相对较低水平的证据,可据此提出临床建议。我们讨论了一位90多岁的女性病例,该女性患者患有典型的MCC原发灶,以及邻近原发淋巴结和引流区域淋巴结的卫星病变,没有淋巴结受累的证据。在这里,我们讨论了治疗的介绍,管理,治疗计划,基本病理,结果和后遗症。我们还将审查新的治疗方式以及最新的分期系统和指南。

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