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Ki-67 expression in non-tumour epithelium adjacent to oral cancer as risk marker for multiple oral tumours.

机译:Ki-67在与口腔癌相邻的非肿瘤上皮中的表达是多种口腔肿瘤的危险标志。

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We have read with great interest and would like to take the opportunity to comment on the recently published article 'Ki-67 expression in non-tumour epithelium adjacent to oral cancer as risk marker for multiple oral tumours' (Gonzalez-Moles et al, 2010). There is a lack of consensus on the duration on which the lesion would be classified as synchronous or metachronous e.g. 6 or more months (Hong et al, 1990), 1 month (Liao et al, 2007) and 2 months (Van der Haring et al, 2009). Such classification appears irrelevant as the treatment and prognosis depend ultimately on clinical and histopath-ological prognosticators. The criteria for secondary primary tumours (SPTs) were erroneously attributed to Billroth (1889), but it was revealed that he did not state such unrealistically rigid criteria (Moertel et al, 1961). The established criteria which are widely used include (i) each of the tumours must present a definite picture of malignancy; (ii) each must be distinct; and (iii) the probability that one was a metastatic lesion from the other must be excluded (Warren and Gates, 1931). Histopathological examination often solves the issue of whether the tumour is malignant, but the other two criteria remain confusing and debatable.
机译:我们非常感兴趣地阅读,并希望借此机会评论最近发表的文章“与口腔癌相邻的非肿瘤上皮中的Ki-67表达是多种口腔肿瘤的危险标志”(Gonzalez-Moles等人,2010年)。对于病变被分类为同步或异时的持续时间缺乏共识,例如6个月或更长时间(Hong等,1990),1个月(Liao等,2007)和2个月(Van der Haring等,2009)。这种分类似乎无关紧要,因为治疗和预后最终取决于临床和组织病理学预后。次生原发性肿瘤(SPTs)的标准被错误地归因于Billroth(1889),但据透露,他没有陈述这种不切实际的严格标准(Moertel等,1961)。广泛使用的既定标准包括:(i)每个肿瘤都必须表现出明确的恶性图像; (ii)每个都必须是不同的; (iii)必须排除一个是转移灶,而另一个是转移灶(Warren and Gates,1931)。组织病理学检查通常可以解决肿瘤是否为恶性的问题,但其他两个标准仍然令人困惑且值得商de。

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