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专家评审在皮肤黑素细胞性病变的组织病理学诊断中仍然很重要。

Expert review remains important in the histopathological diagnosis of cutaneous melanocytic lesions.

作者信息

van Dijk M C R F, Aben K K H, van Hees F, Klaasen A, Blokx W A M, Kiemeney L A L M, Ruiter D J

机构信息

Department of Pathology, University Medical Centre Nijmegen, Nijmegen, and Department of Pathology, University Medical Centre Groningen, Groningen, The Netherlands.

出版信息

Histopathology. 2008 Jan;52(2):139-46. doi: 10.1111/j.1365-2559.2007.02928.x.

Abstract

AIMS

To assess the type of problems encountered in diagnosing melanocytic lesions and to evaluate the contribution of expert review.

METHODS AND RESULTS

Data from 1887 lesions submitted for consultation to one of the expert pathologists of the Dutch Melanoma Working Group Pathology Panel between 1991 and 2004 were analysed. Referring pathologists can voluntarily submit lesions which are difficult to classify to the panel. Most cutaneous melanocytic lesions (n = 1217) were submitted with a presumed diagnosis by the referring pathologists. Relevant underdiagnoses of melanoma (in situ) and overdiagnoses of naevi were prevented in 12% (144/1217) and 15% (178/1217) of cases, respectively. Problematic melanocytic lesions were (i) spitzoid and dysplastic lesions, (ii) lesions with histological features that hampered the diagnosis such as regression, lymphocytic infiltrate, or a combination with other melanocytic lesions, and (iii) lesions with unusual clinical features, e.g. childhood melanoma. Remarkably, the features of the lesions that were submitted and the types of over- and under-diagnosis remained consistent from 1991 to 2004.

CONCLUSIONS

A second opinion from an expert pathologist on problem-prone melanocytic lesions improves patient care, in our series in 27% of cases.

摘要

目的

评估黑色素细胞性病变诊断中遇到的问题类型,并评估专家评审的作用。

方法与结果

分析了1991年至2004年间提交给荷兰黑色素瘤工作组病理小组的一位专家病理学家进行会诊的1887例病变的数据。转诊病理学家可以自愿将难以分类的病变提交给该小组。大多数皮肤黑色素细胞性病变(n = 1217)由转诊病理学家提交时已有初步诊断。分别在12%(144/1217)和15%(178/1217)的病例中避免了黑色素瘤(原位)的相关漏诊和痣的过度诊断。有问题的黑色素细胞性病变包括:(i)梭形和发育异常性病变;(ii)具有妨碍诊断的组织学特征的病变,如消退、淋巴细胞浸润或与其他黑色素细胞性病变合并;(iii)具有不寻常临床特征的病变,如儿童黑色素瘤。值得注意的是,1991年至2004年间提交的病变特征以及过度诊断和漏诊的类型保持一致。

结论

在我们的系列研究中,专家病理学家对易出现问题的黑色素细胞性病变给出的第二种意见在27%的病例中改善了患者护理。

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