B淋系/髓系混合表型急性白血病伴TEL-ABL1融合基因表达1例

R733.71; 混合表型急性白血病(mixed phenotype acute leukemia,MPAL)临床罕见,约占急性白血病的2%~5%.TEL-ABL1融合基因阳性主要见于急性髓细胞白血病(acute myeloid leukemia,AML)、急性淋巴细胞白血病(acute lymphocytic leukemia,ALL)、骨髓增殖性肿瘤(myeloproliferative neoplasm,MPN)等恶性血液系统肿瘤,目前以病例报道为主,均提示预后不良.本例患者B淋系/髓系MPAL伴TEL-ABL1融合基因阳性为首次报道,我们给予针对淋系、髓系白血病化学治疗及酪氨酸激酶抑制...

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Published in复旦学报(医学版) Vol. 49; no. 4; pp. 628 - 632
Main Authors 王露婷, 陆丽娜, 何大保, 刘小敏, 曹淑雅, 王素云
Format Journal Article
LanguageChinese
Published 深圳市龙华区中心医院血液内科 深圳 518110%深圳市龙华区中心医院检验科 深圳 518110 01.07.2022
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ISSN1672-8467
DOI10.3969/j.issn.1672-8467.2022.04.022

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Abstract R733.71; 混合表型急性白血病(mixed phenotype acute leukemia,MPAL)临床罕见,约占急性白血病的2%~5%.TEL-ABL1融合基因阳性主要见于急性髓细胞白血病(acute myeloid leukemia,AML)、急性淋巴细胞白血病(acute lymphocytic leukemia,ALL)、骨髓增殖性肿瘤(myeloproliferative neoplasm,MPN)等恶性血液系统肿瘤,目前以病例报道为主,均提示预后不良.本例患者B淋系/髓系MPAL伴TEL-ABL1融合基因阳性为首次报道,我们给予针对淋系、髓系白血病化学治疗及酪氨酸激酶抑制剂靶向治疗后,达到完全缓解,经巩固化疗后进行人类白细胞抗原(human leucocyte antigen,HLA)相合同胞间异基因外周血造血干细胞移植,患者后因肠道排异反应死亡.
AbstractList R733.71; 混合表型急性白血病(mixed phenotype acute leukemia,MPAL)临床罕见,约占急性白血病的2%~5%.TEL-ABL1融合基因阳性主要见于急性髓细胞白血病(acute myeloid leukemia,AML)、急性淋巴细胞白血病(acute lymphocytic leukemia,ALL)、骨髓增殖性肿瘤(myeloproliferative neoplasm,MPN)等恶性血液系统肿瘤,目前以病例报道为主,均提示预后不良.本例患者B淋系/髓系MPAL伴TEL-ABL1融合基因阳性为首次报道,我们给予针对淋系、髓系白血病化学治疗及酪氨酸激酶抑制剂靶向治疗后,达到完全缓解,经巩固化疗后进行人类白细胞抗原(human leucocyte antigen,HLA)相合同胞间异基因外周血造血干细胞移植,患者后因肠道排异反应死亡.
Author 陆丽娜
王露婷
曹淑雅
王素云
刘小敏
何大保
AuthorAffiliation 深圳市龙华区中心医院血液内科 深圳 518110%深圳市龙华区中心医院检验科 深圳 518110
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Author_FL WANG Su-yun
LU Li-na
CAO Shu-ya
HE Da-bao
LIU Xiao-min
WANG Lu-ting
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B淋系/髓系
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Snippet R733.71; 混合表型急性白血病(mixed phenotype acute leukemia,MPAL)临床罕见,约占急性白血病的2%~5%.TEL-ABL1融合基因阳性主要见于急性髓细胞白血病(acute myeloid leukemia,AML)、急性淋巴细胞白血病(acute lymphocytic...
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Title B淋系/髓系混合表型急性白血病伴TEL-ABL1融合基因表达1例
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