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首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >Interobserver reproducibility among neuropathologists and surgical pathologists in fibrillary astrocytoma grading.
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Interobserver reproducibility among neuropathologists and surgical pathologists in fibrillary astrocytoma grading.

机译:神经病理学家和外科病理学家在原纤维星形细胞瘤分级中观察者间的可重复性。

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摘要

Many of the problems associated with the current grading approaches for fibrillary astrocytomas center around the lack of consistency in grading. This study compares the diagnoses of five neuropathologists with five experienced surgical pathologists with regard to assigning astrocytoma grade. Thirty neoplastic and non-neoplastic lesions were sent to each of five neuropathologists and five surgical pathologists for placement into one of three grades as outlined by modified Ringertz schema. Grading criteria (Burger et al., 1985. Cancer 56:1106-1111) were distributed to all participants, who have been practicing for at least 5 years. An additional category for non-neoplastic or normal tissue was also provided. The diagnoses, based on the majority opinion of the neuropathologist group, included six low grade astrocytomas, 11 anaplastic astrocytomas, seven glioblastoma multiforme, and six normal/reactive lesions. Agreement by all neuropathologists was reached in 12 cases (40%). A discrepant diagnosis was obtained in one of five neuropathologists in 14 additional cases (46.7%). In the remaining four cases, two neuropathologists deviated from the majority opinion; in each of these cases, the diagnostic problem involved differentiating tumor from reactive gliosis. All five surgical pathologists agreed in six cases (20%). One discrepant diagnosis among the surgical pathologist group was seen in seven cases (23.3%). In the remaining 17 cases, two or more discrepant diagnoses were obtained (56.7%); discrepancies in these cases included differences in assignment of tumor grade and in distinguishing low grade astrocytoma from gliosis. In conclusion: (1) it is likely that experience with grading accounts for the better level of agreement among the neuropathologist group (kappa statistic 0.63) versus the surgical pathologist group (kappa statistic 0.36); (2) in most cases, the neuropathologists all agreed or had one discrepant diagnosis (86.7%) versus the surgical pathologist group (43.3%); (3) the discrepancies in diagnosis among both groups is likely related, in good part, to the limitations of the grading schema in fully enumerating the spectrum of such grading parameters as cytologic atypia and vascular proliferation.
机译:与当前纤维原发性星形细胞瘤分级方法相关的许多问题集中在分级一致性的缺乏上。这项研究比较了五位神经病理学家和五位经验丰富的外科病理学家对星形细胞瘤等级的诊断。将三十个赘生性和非赘生性病变分别发送给五名神经病理学家和五名外科手术病理学家,按照改良的林格兹图式将其放置在三个等级之一。将评分标准(Burger等,1985.Cancer 56:1106-1111)分配给已经练习了至少5年的所有参与者。还提供了非肿瘤组织或正常组织的其他类别。根据神经病理学家小组的多数意见,诊断包括六个低度星形细胞瘤,11个间变性星形细胞瘤,七个多形胶质母细胞瘤和六个正常/反应性病变。所有神经病理学家均同意12例(40%)。五名神经病理学家中有一名在另外14例病例中获得了错误的诊断(46.7%)。在其余的四个案例中,两名神经病理学家偏离了多数意见。在每种情况下,诊断问题都涉及区分肿瘤与反应性神经胶质增生。所有五位外科手术病理学家均同意有六例(20%)。手术病理学家组中有7例(23.3%)出现诊断差异。在其余的17例中,获得了两个或更多的差异诊断(56.7%);这些病例的差异包括肿瘤等级分配的差异以及区分低度星形细胞瘤和神经胶质增生的差异。结论:(1)分级经验可能比神经病理学家组(kappa统计量0.63)优于手术病理学家组(kappa统计量0.36)有更好的一致性; (2)在大多数情况下,神经病理学家相对于手术病理学家组(43.3%)都同意或有一个错误的诊断(86.7%); (3)两组之间的诊断差异很可能与分级方案的局限性有关,而分级方案在充分枚举诸如细胞学非典型性和血管增生等分级参数的范围时是有局限性的。

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