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Myeloid tumors accompanying systemic mastocytosis, basophilia, and abnormal platelet-derived growth factor receptor β

机译:骨髓肿瘤随身伴有全身性乳细胞症,嗜碱性菌和异常血小板衍生的生长因子受体β

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INTRODUCTION:Myeloid neoplasms with platelet-derived growth factor receptor β (PDGFRB) rearrangement usually present with eosinophilia in the peripheral blood and bone marrow. Here we report a case of systemic mastocytosis related myeloid neoplasms with basophilia and PRKG2-PDGFRB fusion gene.PATIENTS CONCERNS:A 53-year-old male patient felt fatigue with thrombocythemia and normal hemoglobin over 2?years. Considering the possibility of primary thrombocytosis, the patient was treated with hydroxyurea and interferon. Then the therapy was stopped due to adverse events and worsen condition.DIAGNOSIS:Acute myelogenous leukemia (AML) diagnosis was confirmed by bone marrow morphology and flow cytometry. PDGFRB rearrangement was detected by fluorescence in situ hybridization (FISH) test, with chromosome karyotype 46,XY,t(4:5)(q21:q33). PRKG2-PDGFRB fusion was observed by next generation sequencing (NGS) and verified by RT-PCR followed by Sanger sequencing. The results of bone marrow aspiration, bone marrow biopsy, and immunophenotyping showed systemic mastocytosis-related myeloid tumor with basophilia.INTERVENTIONS:Imatinib 400?mg/d was given on the day of admission. Azacitidine 75?mg/m2 was given for induction therapy for 10?days, and followed by one course of DHAG consolidating therapy. Imatinib was taken orally continuously.OUTCOMES:On the 8th day of treatment, the patient's diet and fatigue improved. The hematological and bone marrow morphological remission was achieved on the 25th day. Cytogenetic complete remission was achieved 3?months later and continued to present (December 20, 2020). PRKG2-PDGFRB fusion gene turned negative 7?months later from diagnosis.LESSONS:Patients with increased basophilic granulocyte and/or mast cells in peripheral blood and/or bone marrow should be screened for PDGFRB abnormality and myeloid or lymphatic tumor. Patients bearing PDGFRB abnormality have a good response to imatinib.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:介绍:骨髓肿瘤,具有血小板衍生的生长因子受体β(PDGFRB)重排通常存在于外周血和骨髓中的嗜酸性粒细胞。在这里,我们向嗜碱性菌和PRKG2-PDGFRB融合基因报告了系统性乳细胞症相关的骨髓肿瘤。患者担心:一个53岁的男性患者患有血小板血症和正常血红蛋白的疲劳。考虑到原发性血小板减少症的可能性,患者用羟基脲和干扰素治疗。然后通过不良事件和恶化病情来停止治疗。肿瘤:骨髓形态和流式细胞术证实了急性骨髓性白血病(AML)诊断。通过荧光原位杂交(鱼)试验检测PDGFRB重排,染色体核型46,XY,T(4:5)(Q21:Q33)。通过下一代测序(NGS)观察PRKG2-PDGFRB融合,并通过RT-PCR验证,然后验证Sanger测序。骨髓抽吸,骨髓活检和免疫蛋白型观察结果显示了与Basophilia的全身性乳细胞增生相关骨髓肿瘤。Incaterventions:Imatinib 400?Mg / D在入场日给出。偶氮辛丁75?Mg / m 2给予诱导治疗10?天,然后进行一系列DHAG综合治疗。伊马替尼不断服用。待办事项:在治疗的第8天,患者的饮食和疲劳改善。血液学和骨髓形态缓解在第25天实现。细胞遗传学完全缓解3?几个月后并继续存在(2020年12月20日)。 PRKG2-PDGFRB融合基因转染值7?几个月后,诊断:患有增加的嗜碱性粒细胞和/或外周血和/或骨髓中的肥大细胞的患者,应筛选PDGFRB异常和髓样或髓样或淋巴瘤。患有PDGFRB异常的患者对伊马替尼的反应良好? 2021提交人。由Wolters Kluwer Health,Inc。出版

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