首页> 美国卫生研究院文献>Blood Cancer Journal >Rationale for revision and proposed changes of the WHO diagnostic criteria for polycythemia vera essential thrombocythemia and primary myelofibrosis
【2h】

Rationale for revision and proposed changes of the WHO diagnostic criteria for polycythemia vera essential thrombocythemia and primary myelofibrosis

机译:修订WHO关于真性红细胞增多症原发性血小板增多症和原发性骨髓纤维化的诊断标准的建议并提出修改建议

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The 2001/2008 World Health Organization (WHO)-based diagnostic criteria for polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (PMF) were recently revised to accomodate new information on disease-specific mutations and underscore distinguishing morphologic features. In this context, it seems to be reasonable to compare first major diagnostic criteria of the former WHO classifications for myeloproliferative neoplasm (MPN) and then to focus on details that have been discussed and will be proposed for the upcoming revision of diagnostic guidelines. In PV, a characteristic bone marrow (BM) morphology was added as one of three major diagnostic criteria, which allowed lowering of the hemoglobin/hematocrit threshold for diagnosis, which is another major criterion, to 16.5 g/dl/49% in men and 16 g/dl/48% in women. The presence of a JAK2 mutation remains the third major diagnostic criterion in PV. Subnormal serum erythropoietin level is now the only minor criterion in PV and is used to capture JAK2-unmutated cases. In ET and PMF, mutations that are considered to confirm clonality and specific diagnosis now include CALR, in addition to JAK2 and MPL. Also in the 2015 discussed revision, overtly fibrotic PMF is clearly distinguished from early/prefibrotic PMF and each PMF variant now includes a separate list of diagnostic criteria. The main rationale for these changes was to enhance the distinction between so-called masked PV and JAK2-mutated ET and between ET and prefibrotic early PMF. The proposed changes also underscore the complementary role, as well as limitations of mutation analysis in morphologic diagnosis. On the other hand, discovery of new biological markers may probably be expected in the future to enhance discrimination of the different MPN subtypes in accordance with the histological BM patterns and corresponding clinical features.
机译:最近修订了基于2001/2008世界卫生组织(WHO)的真性红细胞增多症(PV),原发性血小板增多症(ET)和原发性骨髓纤维化(PMF)的诊断标准,以适应有关疾病特异性突变的新信息,并强调区分形态特征。在这种情况下,比较前世界卫生组织对骨髓增生性肿瘤(MPN)的WHO分类的主要诊断标准,然后集中讨论已讨论的细节,并为即将修订的诊断指南提出建议,似乎是合理的。在PV中,增加了特征性的骨髓(BM)形态作为三项主要的诊断标准之一,这使诊断的血红蛋白/血细胞比容阈值(这是另一项主要标准)降至男性的16.5μg/ dl / 49%女性为16μg/ dl / 48%。 JAK2突变的存在仍然是PV中的第三个主要诊断标准。血清促红细胞生成素水平低于正常水平现在是PV中的唯一次要标准,可用于捕获未突变JAK2的病例。在ET和PMF中,除JAK2和MPL外,现在被认为可以确认克隆性和特定诊断的突变还包括CALR。同样在2015年讨论的修订版中,明显的纤维化PMF与早期/纤维化前PMF明显不同,并且每个PMF变体现在都包括单独的诊断标准列表。这些改变的主要原理是增强所谓的掩蔽PV和JAK2突变的ET之间以及ET和纤维化前早期PMF之间的区别。提出的更改还强调了互补作用,以及突变分析在形态学诊断中的局限性。另一方面,根据组织学BM模式和相应的临床特征,将来可能会期望发现新的生物标志物,以增强对不同MPN亚型的区分。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号