Kirito Keita
Department of Hematology/Oncology, University of Yamanashi, Chuo 409-3898, Japan.
Rinsho Byori. 2012 Jun;60(6):553-9.
Although the fourth edition of the World Health Organization (WHO) classification of the diagnostic criteria for myeloproliferative neoplasms is widely accepted, the diagnosis of essential thrombocythemia has been debated. One of the controversies focuses on the provisional entity known as refractory anemia, which exhibits ringed sideroblasts associated with marked thrombocytosis (RARS-T). To date, it has not been made clear whether RARS-T is a form of ET or a separate and unique disease entity. Recent findings, which may shed light on this debate, have demonstrated that more than 60% of RARS-T patients exhibit somatic mutations of SF3B1, a gene encoding a core component of the RNA-splicing system. Another debate is focused on the role of bone marrow histopathology in the diagnosis of essential thrombocythemia. Bone marrow histopathology has been considered to be a major diagnostic criterion for essential thrombocythemia since the previous version of the WHO classification criteria was published. The histological features of bone marrow are important to distinguish essential thrombocythemia from early, prefibrotic stages of primary myelofibrosis, which frequently exhibit elevated platelet levels. The specific histological bone marrow patterns of the diseases were outlined in the fourth version of the WHO classification; however, several investigators have claimed that the criteria exhibit poor interobserver reproducibility and are not sufficiently robust to discriminate essential thrombocythemia and early-stage primary myelofibrosis. This review highlights the recent debates on the role of bone marrow histopathology in essential thrombocythemia.
尽管世界卫生组织(WHO)髓系增殖性肿瘤诊断标准的第四版已被广泛接受,但原发性血小板增多症的诊断一直存在争议。其中一个争议焦点集中在一种称为难治性贫血伴环形铁粒幼细胞和显著血小板增多症(RARS-T)的临时实体。迄今为止,RARS-T究竟是原发性血小板增多症的一种形式还是一种独立且独特的疾病实体尚不清楚。近期的研究发现或许能为这场争论提供线索,这些发现表明超过60%的RARS-T患者存在SF3B1的体细胞突变,SF3B1是一种编码RNA剪接系统核心成分的基因。另一个争论焦点是骨髓组织病理学在原发性血小板增多症诊断中的作用。自WHO分类标准的上一版发布以来,骨髓组织病理学一直被视为原发性血小板增多症的主要诊断标准。骨髓的组织学特征对于区分原发性血小板增多症与原发性骨髓纤维化的早期、纤维化前期阶段很重要,原发性骨髓纤维化前期阶段常常血小板水平升高。WHO分类的第四版概述了这些疾病特定的骨髓组织学模式;然而,一些研究者声称这些标准在观察者之间的可重复性较差,并且不足以有力地区分原发性血小板增多症和早期原发性骨髓纤维化。这篇综述重点介绍了近期关于骨髓组织病理学在原发性血小板增多症中作用的争论。