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骨髓形态学是慢性嗜酸性白血病、未分类和反应性特发性嗜酸性粒细胞增多综合征之间的有力鉴别诊断依据。

Bone marrow morphology is a strong discriminator between chronic eosinophilic leukemia, not otherwise specified and reactive idiopathic hypereosinophilic syndrome.

机构信息

Department of Hematopathology, M.D. Anderson Cancer Center, Houston, TX, USA

Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Haematologica. 2017 Aug;102(8):1352-1360. doi: 10.3324/haematol.2017.165340. Epub 2017 May 11.

Abstract

Chronic eosinophilic leukemia, not otherwise specified can be difficult to distinguish from idiopathic hypereosinophilic syndrome according to the current World Health Organization guideline. To examine whether the morphological features of bone marrow might aid in the differential diagnosis of these two entities, we studied a total of 139 patients with a diagnosis of chronic eosinophilic leukemia, not otherwise specified (n=17) or idiopathic hypereosinophilic syndrome (n=122). As a group, abnormal bone marrow morphological features, resembling myelodysplastic syndromes, myeloproliferative neoplasm or myelodysplastic/myeloproliferative neoplasm, were identified in 40/139 (27%) patients: 16 (94%) of those with chronic eosinophilic leukemia and 24 (20%) of those with hypereosinophilic syndrome. Abnormal bone marrow correlated with older age (<0.001), constitutional symptoms (<0.001), anemia (=0.041), abnormal platelet count (=0.002), organomegaly (=0.008), elevated lactate dehydrogenase concentration (=0.005), abnormal karyotype (<0.001), as well as the presence of myeloid neoplasm-related mutations (<0.001). Patients with abnormal bone marrow had shorter survival (48.1 months not reached, <0.001), a finding which was independent of other confounding factors (<0.001). The association between abnormal bone marrow and shorter survival was also observed in hypereosinophilic syndrome patients alone. In summary, most patients with chronic eosinophilic leukemia, not otherwise specified and a proportion of those with idiopathic hypereosinophilic syndrome show abnormal bone marrow features similar to the ones encountered in patients with myelodysplastic syndromes, myelodysplastic/myeloproliferative neoplasm or -negative myeloproliferative neoplasm. Among patients who are currently considered to have idiopathic hypereosinophilic syndrome, abnormal bone marrow is a strong indicator of clonal hematopoiesis. Similar to other myeloid neoplasms, bone marrow morphology should be one of the major criteria to distinguish patients with chronic eosinophilic leukemia, not otherwise specified or clonal hypereosinophilic syndrome from those with truly reactive idiopathic hypereosinophilic syndrome.

摘要

根据现行世界卫生组织指南,慢性嗜酸粒细胞白血病,非特指型与特发性嗜酸粒细胞增多综合征较难区分。为了研究骨髓形态学特征是否有助于这两种疾病的鉴别诊断,我们共研究了 139 例诊断为慢性嗜酸粒细胞白血病,非特指型(n=17)或特发性嗜酸粒细胞增多综合征(n=122)的患者。作为一个整体,有 40/139(27%)例患者的骨髓形态学表现异常,类似于骨髓增生异常综合征、骨髓增生性肿瘤或骨髓增生异常/骨髓增生性肿瘤:16(94%)例慢性嗜酸粒细胞白血病患者和 24(20%)例特发性嗜酸粒细胞增多综合征患者。骨髓形态学异常与年龄较大(<0.001)、全身症状(<0.001)、贫血(=0.041)、血小板计数异常(=0.002)、器官肿大(=0.008)、乳酸脱氢酶浓度升高(=0.005)、核型异常(<0.001)以及存在髓系肿瘤相关突变(<0.001)相关。骨髓形态学异常的患者生存时间更短(48.1 个月未达到,<0.001),这一发现独立于其他混杂因素(<0.001)。这一结果在特发性嗜酸粒细胞增多综合征患者中同样存在。总之,大多数慢性嗜酸粒细胞白血病,非特指型患者和一部分特发性嗜酸粒细胞增多综合征患者存在类似于骨髓增生异常综合征、骨髓增生异常/骨髓增生性肿瘤或骨髓增生性肿瘤-阴性患者的骨髓形态学异常。在目前被认为是特发性嗜酸粒细胞增多综合征的患者中,骨髓形态学异常是克隆性造血的强烈指征。与其他髓系肿瘤一样,骨髓形态学应该是将慢性嗜酸粒细胞白血病,非特指型或克隆性嗜酸粒细胞增多综合征患者与真正的反应性特发性嗜酸粒细胞增多综合征患者区分开来的主要标准之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628b/5541870/89aa756cbb2b/1021352.fig1.jpg

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