Degree of fibrosis and its association with angiogenesis in the myelofibrotic bone marrow

S. Afroz, A. Kabir, B. P. Dey, M. M. Rahman, Papiya Rahman, Rezwana Karim, Syeeda Shiraj Um Mahmuda, Umama-Tun-Nesa Emita, S. Jahan
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Abstract

Background: Primary and secondary myelofibrosis has become a global burden due to its increased mortality and morbidity. Angiogenesis is a significant driving force in the development of fibrogenesis in the bone marrow, which leads to myelofibrosis. The microvascular density (MVD) with immunomarker CD34 can be used to assess the degree of angiogenesis. The objective of this study was to examine the association between degree of myelofibrosis and angiogenesis in hematological malignancies. Methods: Forty-six trephine biopsy specimens of various hematological malignancies with myelofibrosis were studied at the Department of Pathology of Bangabandhu Sheikh Mujib Medical University. Extent of myelofibrosis in each case was assessed by examining the reticulin and Masson’s trichrome stained sections using a semiquantitative grading system of bone marrow fibrosis (MF) within a scale of MF-0 to MF-3. Angiogenesis was measured by counting MVD in the ‘hotspots’ after immunostaining with CD34 antibody. Results: The trephine biopsy cases were grouped into early fibrotic (MF-1) and advanced fibrotic (MF-2,3) consisting of 16 (34.8%) and 30 (65.2%) patients, respectively. Angiogenesis was estimated as mean MVD count which revealed 16.7 ± 5.4 and 32.0 ± 11.5 in these groups, respectively.  Significant difference of mean MVD values     (P<0.001) between the early and advanced fibrotic groups revealed the association of angiogenesis and degree of myelofibrosis. Conclusion: MVD may be used to measure angiogenesis in myelofibrotic marrow along with other clinical and laboratory indices as a marker of disease activity in hematological malignancies, thus aiding disease prognosis. Bangabandhu Sheikh Mujib Medical University Journal 2023;16(1): 26-34  
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骨髓纤维化骨髓的纤维化程度及其与血管生成的关系
背景:原发性和继发性骨髓纤维化由于其死亡率和发病率的增加而成为全球负担。血管生成是导致骨髓纤维化的骨髓纤维化发展的重要驱动力。免疫标记CD34的微血管密度(MVD)可用于评估血管生成的程度。本研究的目的是检测血液系统恶性肿瘤中骨髓纤维化程度与血管生成之间的关系。方法:在Bangabandhu Sheikh Mujib医科大学病理学系对46例伴有骨髓纤维化的各种血液系统恶性肿瘤的环钻活检标本进行研究。通过使用骨髓纤维化(MF)的半定量分级系统在MF-0至MF-3的范围内检查网织蛋白和Masson三色染色切片来评估每个病例的骨髓纤维化程度。用CD34抗体免疫染色后,通过计数“热点”中的MVD来测量血管生成。结果:环钻活检病例分为早期纤维化(MF-1)和晚期纤维化(MF-2,3),分别为16例(34.8%)和30例(65.2%)。血管生成被估计为平均MVD计数,在这些组中分别为16.7±5.4和32.0±11.5。早期和晚期纤维化组的平均MVD值存在显著差异(P<0.001),表明血管生成与骨髓纤维化程度有关。结论:MVD可用于测量骨髓纤维化骨髓中的血管生成,以及其他临床和实验室指标,作为血液系统恶性肿瘤疾病活动性的标志,从而帮助疾病预后。Bangabandhu Sheikh Mujib医科大学学报2023;16(1):26-34
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