Helmbold P, Schröter S, Holzhausen H-J, Dunst J, Marsch W Ch
Universitätsklinik und Poliklinik für Dermatologie und Venerologie der Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany.
Hautarzt. 2002 Oct;53(10):652-8. doi: 10.1007/s00105-001-0318-4.
Merkel cell carcinoma (cutaneous neuroendocrine carcinoma) is an uncommon, highly malignant, neuroendocrine skin tumour. Typically, the primary is a fast-growing tough dermal nodule that is characterized histologically by uniform round cells with a small cytoplasmic rim. The tumour cells express the cytokeratins 8, 18, 19, 20, neurofilament, synaptophysin, chromogranin, and neuron-specific enolase. A high frequency of local recurrences (25-77%) and lymph-node metastases (50%) are characteristic features of Merkel cell carcinoma. The 5-year survival rate is 30-74%. Merkel cell carcinomas are highly radiosensitive. Thus, besides surgical methods, radiation should be included into the treatment concept in every stage. We present four cases of Merkel cell carcinoma with different courses for a review-like discussion of this disease giving instructions for rapid diagnosis and effective therapy.
默克尔细胞癌(皮肤神经内分泌癌)是一种罕见的、高度恶性的神经内分泌皮肤肿瘤。通常,原发灶是一个快速生长的坚硬真皮结节,组织学上其特征为具有少量细胞质边缘的均匀圆形细胞。肿瘤细胞表达细胞角蛋白8、18、19、20、神经丝、突触素、嗜铬粒蛋白和神经元特异性烯醇化酶。局部复发(25%-77%)和淋巴结转移(50%)的高发生率是默克尔细胞癌的特征性表现。5年生存率为30%-74%。默克尔细胞癌对放疗高度敏感。因此,除手术方法外,放疗应纳入各阶段的治疗方案中。我们呈现4例病程各异的默克尔细胞癌病例,以进行类似综述的讨论,为这种疾病的快速诊断和有效治疗提供指导。