IF 2 3区 医学 Q2 PEDIATRICS BMC Pediatrics Pub Date : 2025-02-28 DOI:10.1186/s12887-024-05093-3
Taxiarhia J Arabatzis, Biren Desai, Sandra Baril, Susan Rasul, Girmay Tekle-Yohannes, Michal Ann Miller
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引用次数: 0

摘要

我们在此描述一例在出生后第 4 天被偶然诊断为先天性 KMT2A 重排(KMT2A-r)B 细胞 ALL 的婴儿。他在出生后第 5 天接受了首剂鞘内甲氨蝶呤治疗,并于出生后第 6 天接受了诱导性全身治疗。最小残留病灶(MRD)为1.4%。巩固和免疫治疗后,他出现了孤立的中枢神经系统疾病。8个月大时,他接受了造血干细胞移植(HSCT)。14个月大时,他的髓质和中枢神经系统复发,16个月大时接受了CD19 CAR-T治疗。6 岁时,他的病情仍在缓解,发育迟缓可以忍受,生活质量良好。
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A long-term survivor of congenital KMT2A-R B-lymphoblastic leukemia with persistently positive bone marrow MRD and multiple CNS relapses.

Here we describe the case of an infant incidentally diagnosed with congenital KMT2A-rearranged (KMT2A-r) B-cell ALL on Day of Life 4. He received the first dose of intrathecal methotrexate on DOL 5, and induction systemic therapy on DOL 6. He demonstrated morphologic remission at the end of induction but had positive bone marrow. Minimal residual disease (MRD) was 1.4%. He experienced isolated CNS disease after consolidation and immunotherapy. At 8 months of age he underwent hematopoietic stem cell transplantation (HSCT). At 14 months of age he had medullary and CNS relapse, and at 16 months of age underwent CD19 CAR-T therapy. At 6 years of age he remains in remission with tolerable developmental delays and a good quality of life.

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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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