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基于 WHO 2008 标准的骨髓纤维化的鉴别诊断:伴有骨髓纤维化的急性全髓增生、伴有骨髓纤维化的急性巨核细胞白血病、原发性骨髓纤维化和骨髓增生异常综合征伴骨髓纤维化。

Differential diagnosis of myelofibrosis based on WHO 2008 criteria: acute panmyelosis with myelofibrosis, acute megakaryoblastic leukemia with myelofibrosis, primary myelofibrosis and myelodysplastic syndrome with myelofibrosis.

机构信息

Department of Laboratory Medicine, VHS Medical Center, Seoul, South Korea; Department of Laboratory Medicine, College of Medicine and Asan Medical Center, University of Ulsan, Seoul, South Korea.

出版信息

Int J Lab Hematol. 2013 Dec;35(6):629-36. doi: 10.1111/ijlh.12101. Epub 2013 May 22.

Abstract

INTRODUCTION

The aim of this study was to characterize clinicopathological features of acute panmyelosis with myelofibrosis (APMF), acute megakaryoblastic leukemia with myelofibrosis (AMKL-MF), primary myelofibrosis (PMF) and myelodysplastic syndrome with myelofibrosis (MDS-MF) in order to provide the keys to the differential diagnosis of bone marrow (BM) fibrosis.

METHODS

We compared age, gender, splenomegaly, serum lactate dehydrogenase level, blood cell counts, blast counts in peripheral blood (PB) and BM, megakaryocyte counts, BM cellularity, dysplasia, and the karyotypes of patients with APMF (n = 6), AMKL-MF (n = 7), PMF (n = 44), and MDS-MF (n = 44).

RESULTS

APMF showed hyperplasia of all three lineages, increase in megakaryocyte count with dysplasia and frequent abnormal karyotypes. AMKL-MF was associated with elevated BM blast counts, decreased BM megakaryocyte count with rare megakaryocytic dysplasia and chromosome 21 abnormality. PMF patients displayed splenomegaly, rare blasts in PB/BM, and JAK2 V617F mutation. MDS-MF patients showed pancytopenia, dysplasia in all three lineages and recurrent chromosomal abnormalities involving chromosome 5,7,12, and 17.

CONCLUSIONS

Although differential diagnosis among APMF, AMKL-MF, PMF, and MDS-MF is very challenging due to the overlapping clinical and morphological features, meticulous investigation of the patient with respect to splenomegaly, blood cell count, PB and BM findings, and karyotype will serve as a guide to correct diagnosis.

摘要

简介

本研究旨在对急性全髓增生伴骨髓纤维化(APMF)、急性巨核细胞白血病伴骨髓纤维化(AMKL-MF)、原发性骨髓纤维化(PMF)和骨髓增生异常综合征伴骨髓纤维化(MDS-MF)的临床病理特征进行分析,以期为骨髓纤维化的鉴别诊断提供线索。

方法

我们比较了 APMF(n=6)、AMKL-MF(n=7)、PMF(n=44)和 MDS-MF(n=44)患者的年龄、性别、脾肿大、血清乳酸脱氢酶水平、血细胞计数、外周血和骨髓中原始细胞计数、巨核细胞计数、骨髓细胞增生程度、发育不良以及核型。

结果

APMF 表现为三系增生过度,巨核细胞计数增加,伴有发育不良,且常伴有异常核型。AMKL-MF 与骨髓中原始细胞计数升高、骨髓巨核细胞计数减少、罕见巨核细胞发育不良和 21 号染色体异常相关。PMF 患者表现为脾肿大、外周血/骨髓中原始细胞罕见,且存在 JAK2 V617F 突变。MDS-MF 患者表现为全血细胞减少,三系发育不良,常伴有 5 号、7 号、12 号和 17 号染色体的反复异常。

结论

虽然 APMF、AMKL-MF、PMF 和 MDS-MF 的鉴别诊断由于其重叠的临床和形态学特征而极具挑战性,但详细的患者检查包括脾肿大、血细胞计数、外周血和骨髓发现以及核型分析,有助于指导正确诊断。

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