首页> 外文期刊>International Journal of Clinical Medicine >Successful Treatment of Life-Threatening Cerebral Bleeding Associated with Disseminated Intravascular Coagulation Using Recombinant Human Soluble Thrombomodulin in a Patient with Mixed Phenotype Acute Leukemia with t (9; 22) (q34; q11.2); Bcr-Abl1
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Successful Treatment of Life-Threatening Cerebral Bleeding Associated with Disseminated Intravascular Coagulation Using Recombinant Human Soluble Thrombomodulin in a Patient with Mixed Phenotype Acute Leukemia with t (9; 22) (q34; q11.2); Bcr-Abl1

机译:使用重组人可溶性血栓调节蛋白成功治疗t型混合型表型急性白血病患者的危及生命的脑出血与弥散性血管内凝血相关联(t; 9; 22)(q34; q11.2); Bcr-Abl1

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Recently, mixed phenotype acute leukemia (MPAL) with t (9; 22) (q34; q11.2); bcr-abl1 was described as one kind of acute leukemia of ambiguous lineage in the 2008 World Health Organization Classification of Tumors of Hematopoietic and Lymphoid Tissues. However, treatment strategy remains difficult for this uncommon MPAL. In addition, this type of MPAL is at high risk of tumor lysis syndrome (TLS) because of high chemo-sensitivity. Here, we report a MPAL with t (9; 22) (q34; q11.2); bcr-abl1 case that suffered from life-threatening cerebral bleeding associated with disseminated intravascular coagulation (DIC) with TLS after bcr-abl positive acute lymphoblastic leukemia (ALL) type induction therapy who was successfully treated with recombinant human thrombomodulin (rhTM). This case reached complete remission without additive cerebral bleeding. In conclusion, bcr-abl positive ALL type induction therapy was effective for MPAL with t (9; 22) (q34; q11.2); bcr-abl1 and rhTM was effective against DIC with TLS.
机译:最近,混合表型急性白血病(MPAL)与t(9; 22)(q34; q11.2); bcr-abl1在2008年世界卫生组织《造血和淋巴组织肿瘤分类》中被描述为一种歧义性急性白血病。但是,对于这种罕见的MPAL,治疗策略仍然很困难。另外,由于高的化学敏感性,这种类型的MPAL处于高的肿瘤溶解综合征(TLS)风险中。在这里,我们报告的MPAL为t(9; 22)(q34; q11.2); bcr-abl1病例,在通过bcr-abl阳性急性淋巴细胞白血病(ALL)诱导治疗后,通过重组人血栓调节蛋白(rhTM)成功治疗,并伴有TLS的弥散性血管内凝血(DIC)和致命性脑出血。该病例达到完全缓解,无附加脑出血。总之,bcr-abl阳性ALL型诱导治疗对MPAL有效,t(9; 22)(q34; q11.2); bcr-abl1和rhTM对带TLS的DIC有效。

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