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首页> 外文期刊>Pathology oncology research: POR >Epidemiological, Clinicopathological and Virological Features of Merkel Cell Carcinomas in Medical Center of University of Pécs, Hungary (2007–2012)
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Epidemiological, Clinicopathological and Virological Features of Merkel Cell Carcinomas in Medical Center of University of Pécs, Hungary (2007–2012)

机译:匈牙利佩奇大学医学中心的默克尔细胞癌的流行病学,临床病理和病毒学特征(2007-2012年)

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Merkel cell carcinoma (MCC) is a rare, highly aggressive skin tumour. In 2008, a Merkel cell polyomavirus (MC) was identified in MCCs as a potential etiological factor of MCC. The aims of this retrospective study were to investigate the epidemiological, clinicopathological and virological features of MCCs. Between 2007 and 2012, 11 patients had been diagnosed with MCC by histological methods in University of Pécs, Hungary. In eight MCC cases MC was tested by PCR (in primary skin lesions, lymph nodes/cutan metastases, MCC neighboring carcinomas). Clinicopathological characteristics (age, histological pattern, lymphovascular invasion, co-morbidities) of MC-positive and MC-negative cases were compared. MC was detected in three (37.5?%) out of eight patients’ primary tumour or metastasis. The average age was 73.8 (64.3 in MC-positive group). Except the youngest, 55?year-old patient (the primary tumour appeared on his leg), all tumours were found at the head and neck region. Immunosuppression (steroid therapy, chronic lymphoid leukaemia, chronic obstructive pulmonary disease) and/or old age were characteristic for all cases. Histological pattern was different in MC-positive and in MC-negative groups: MCCs with MC showed more homogeneous histological pattern, lack of lymphovascular invasion and were associated with better prognosis (mortality rate: 33?% versus 80?%). MCC associated with oncogenic virus is a newly recognized clinical entity. However, MC could not be detected in all histologically proven MCCs. The well-defined selection of patients/disease groups and better characterization of differences between MC-positive and negative cases is an important step towards the recognition of the etiology and pathogenesis of all MCCs.
机译:默克尔细胞癌(MCC)是一种罕见的高度侵袭性皮肤肿瘤。 2008年,在MCC中发现了默克尔细胞多瘤病毒(MC)作为MCC的潜在病因。这项回顾性研究的目的是调查MCC的流行病学,临床病理学和病毒学特征。在2007年至2012年之间,匈牙利佩奇大学通过组织学方法诊断出11例MCC患者。在8例MCC病例中,通过PCR检测MC(在原发性皮肤病变,淋巴结/角质转移,MCC邻近癌中)。比较了MC阳性和MC阴性病例的临床病理特征(年龄,组织学模式,淋巴血管浸润,合并症)。在八名患者的原发肿瘤或转移中,三分之二(37.5%)被检测到MC。平均年龄为73.8岁(MC阳性组为64.3岁)。除了最年轻的55岁患者(原发肿瘤出现在他的腿上)以外,所有肿瘤均位于头部和颈部。免疫抑制(类固醇疗法,慢性淋巴白血病,慢性阻塞性肺疾病)和/或老年是所有病例的特征。 MC阳性和MC阴性组的组织学模式不同:MC的MCC显示出更均一的组织学模式,缺乏淋巴管浸润并且预后更好(死亡率:33%vs 80%)。与致癌病毒相关的MCC是新近公认的临床实体。但是,无法在所有经过组织学证实的MCC中检测到MC。明确定义患者/疾病组的选择以及更好地表征MC阳性和阴性病例之间的差异是认识所有MCC的病因和发病机制的重要一步。

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