首页> 外文期刊>Journal of cutaneous pathology >Lymph nodal Merkel cell carcinoma: primary tumor or metastasis from unknown primary site?
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Lymph nodal Merkel cell carcinoma: primary tumor or metastasis from unknown primary site?

机译:淋巴结性默克尔细胞癌:原发灶或原发灶未知转移?

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摘要

Merkel cell carcinoma represents rare, aggressive skin cancer with neuroendocrine differentiation. Most Merkel cell carcinomas develop within the skin of the head and neck or on the extremities; in <10% of cases, the trunk or mucus membranes are involved. Regional lymph node metastases occur in 50-66% of cases.In 1992, Eusebi et al. described eight cases of nodal Merkel cell carcinoma in the absence of an identifiable primary malignancy. Since that time, other authors ' have reported cases of 'primary' nodal Merkel cell carcinoma and have raised the issue of whether this phenomenon truly occurs or whether such nodal involvement represents, instead, metastasis from an occult tumor. In such cases, strict criteria should be applied before rendering a diagnosis of primary nodal Merkel cell carcinoma. In addition, there is need for specific immunohisto-chemical evidence to support the diagnosis.
机译:默克尔细胞癌代表具有神经内分泌分化的罕见,侵袭性皮肤癌。大多数默克尔细胞癌会在头颈部皮肤或四肢内发展。在少于10%的情况下,会累及躯干或粘膜。局部淋巴结转移发生在50-66%的病例中。1992年,Eusebi等人。他描述了8例淋巴结性默克尔细胞癌,其中没有可确定的原发性恶性肿瘤。从那时起,其他作者报告了“原发性”淋巴结默克尔细胞癌病例,并提出了这种现象是否确实发生或这种淋巴结转移是否代表隐匿性肿瘤转移的问题。在这种情况下,应在诊断原发性结节性默克尔细胞癌之前应用严格的标准。另外,需要特定的免疫组织化学证据来支持诊断。

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