Brucellosis complicated by myelofibrosis: report of five cases and review of literature.

IF 1.1 Q4 ONCOLOGY International journal of clinical and experimental pathology Pub Date : 2023-01-01
Jun-Nuan Wang, Bing-Jie Li, Jun Yuan, Yan Li
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Abstract

Myelofibrosis is a myeloproliferative tumor, that can be secondary to malignant hematologic or inflammatory diseases, such as chronic myeloid leukemia, polycythemia vera, primary thrombocythemia, multiple myeloma, disseminated tuberculosis, or vasculitis. However, few cases of brucellosis-associated myelofibrosis have been reported. Moreover, due to the rarity of this phenomenon, it is often overlooked by clinicians, resulting in misdiagnosis and mismanagement. Thus, brucellosis should be considered as a possible cause of myelofibrosis. In the present study, we report five cases of brucellosis, of which three had myelofibrosis. In addition, to further determine the potential link between brucellosis and myelofibrosis, we retrospectively analyzed the levels of various cytokines by collecting the clinicopathologic data of patients and using immunohistochemical staining. We found that brucellosis patients with myelofibrosis had elevated levels of cytokines such as interferon (IFN)-γ, interleukin (IL)-1β, basic fibroblast growth factor (b-FGF), vascular endothelial growth factor (VEGF), suggesting that the regulation of cytokines may play a central role in the development of myelofibrosis in patients with brucellosis.

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布鲁氏菌病合并骨髓纤维化:附5例报告并文献复习。
骨髓纤维化是一种骨髓增生性肿瘤,可继发于恶性血液病或炎症性疾病,如慢性髓性白血病、真性红细胞增多症、原发性血小板增多症、多发性骨髓瘤、弥散性结核或血管炎。然而,很少有布鲁氏菌病相关的骨髓纤维化病例被报道。此外,由于这种现象的罕见性,往往被临床医生忽视,导致误诊和管理不善。因此,布鲁氏菌病应被认为是骨髓纤维化的可能原因。在本研究中,我们报告了5例布鲁氏菌病,其中3例有骨髓纤维化。此外,为了进一步确定布鲁氏菌病与骨髓纤维化之间的潜在联系,我们通过收集患者的临床病理资料并使用免疫组织化学染色,回顾性分析了各种细胞因子的水平。我们发现伴有骨髓纤维化的布鲁氏菌病患者的细胞因子水平升高,如干扰素(IFN)-γ、白细胞介素(IL)-1β、碱性成纤维细胞生长因子(b-FGF)、血管内皮生长因子(VEGF),这表明细胞因子的调节可能在布鲁氏菌病患者骨髓纤维化的发展中起核心作用。
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来源期刊
自引率
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发文量
42
审稿时长
1 months
期刊介绍: The International Journal of Clinical and Experimental Pathology (IJCEP, ISSN 1936-2625) is a peer reviewed, open access online journal. It was founded in 2008 by an international group of academic pathologists and scientists who are devoted to the scientific exploration of human disease and the rapid dissemination of original data. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal.
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