首页> 外文期刊>Cytopathology >Proffered papers 14.00-15.00 Tuesday 16 September 2003.
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Proffered papers 14.00-15.00 Tuesday 16 September 2003.

机译:发表论文14.00-15.00 2003年9月16日星期二。

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We promote FNA as the first line investigation for lymphadenopathy. Patients subjected to FNA have direct smears and needle rinses routinely prepared for morphological interpretation and, if appropriate, immunosuspension (using immunoflourescence and FACS), immunostaining, microbiology investigations, and PCR. Patients with a cytological diagnosis of lymphoma are then subjected to surgical biopsy if clinically appropriate. We are aware that in many haemato-oncology services, especially those where the pathologist has only limited experience of cytology, FNA is regarded as either inferior to histology, or of no use, in identifying and classifying lymphomas. In this audit we address this misconception. All cases coded by SNOMED as lymphoma at St George's between January 2000 and December 2002 were retrieved and their diagnostic pathway was reviewed. We identified those cases that had preceding FNA from those that did not, and we determined which samples had which ancillary tests. Our audit shows that: *FNA is highly sensitive for B-cell lymphoma, which is increased by immunosuspension studies to 100%. *FNA has a lower sensitivity for T-cell lymphoma, which is slightly increased by immunosuspension studies to 73%. *FNA has a lower sensitivity for Hodgkin lymphoma of 73%, which is not increased by immunosuspension studies. *We do not use PCR enough for statistically significant data on its utility. *Core biopsy provides no information than cannot be obtained by FNA. We conclude that: *FNA is an appropriate means of identifying and classifying lymphoma. *The utility of FNA is greatly enhanced by ancillary tests, especially immunosuspension studies. *Core biopsy is no better than FNA for diagnosing and classifying lymphoma. *Excision biopsy is still important in the comprehensive documentation of lymphoma. *Excision biopsy is an essential second line investigation in cases where the lymphadenopathy persists or progresses regardless of the FNA findings.
机译:我们促进FNA作为淋巴结病的一线研究。进行FNA的患者应常规常规涂片和针头冲洗,以进行形态学解释,必要时还可以进行免疫悬浮(使用免疫荧光和FACS),免疫染色,微生物学研究和PCR。如果临床合适,对具有淋巴瘤细胞学诊断的患者进行手术活检。我们知道,在许多血液肿瘤学服务中,特别是那些病理学家仅具有细胞学经验的服务中,FNA在识别和分类淋巴瘤方面被认为不如组织学,或者没有用。在这次审核中,我们解决了这个误解。检索了2000年1月至2002年12月在圣乔治被SNOMED编码为淋巴瘤的所有病例,并对其诊断途径进行了回顾。我们从没有FNA的病例中识别出了那些病例,并确定了哪些样品具有哪些辅助检查。我们的审计表明:* FNA对B细胞淋巴瘤高度敏感,通过免疫悬浮研究可将其增加到100%。 * FNA对T细胞淋巴瘤的敏感性较低,通过免疫悬浮研究可稍微提高到73%。 * FNA对霍奇金淋巴瘤的敏感性较低,为73%,而免疫悬浮研究并未提高这种敏感性。 *我们对PCR的效用没有足够的统计意义上的重要数据。 *核心活检没有提供FNA无法获得的信息。我们得出以下结论:* FNA是识别和分类淋巴瘤的合适方法。 * FNA的实用性通过辅助测试(尤其是免疫悬浮研究)大大增强。 *对于淋巴瘤的诊断和分类,核心活检并不比FNA好。 *在淋巴瘤的全面文献中,活检仍很重要。 *无论FNA是否发现,淋巴结病持续或进展的情况下,活检是必不可少的二线检查。

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