TTMV::RARA阳性急性早幼粒细胞白血病复发时伴有骨髓坏死和中枢神经系统受累。

IF 0.9 Q4 HEMATOLOGY
Zhao Wang, Jiaqi Chen, Juanxia Meng, Mingfeng Zhao, Hongxing Liu, Xia Xiao
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引用次数: 0

摘要

自2021年Astolfi等人在类似急性早幼粒细胞白血病(APL)的儿科病例中发现TTMV::RARA融合基因以来,全球已有多例类似病例报道。在本报告中,我们介绍了一例青少年 APL 复发病例,患者携带 TTMV::RARA 融合基因。该患者表现出广泛的中枢神经系统受累,并在疾病复发期间出现骨髓坏死。尽管患者在再次接受化疗后病情得到完全缓解,但很快又再次复发,这凸显了该亚型极具侵袭性的特点。这些临床表现使人们对这种罕见疾病的认识不断提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TTMV::RARA-positive acute promyelocytic leukemia with marrow necrosis and central nervous system involvement at disease recurrence.

Since the identification of the TTMV::RARA fusion in pediatric cases resembling acute promyelocytic leukemia (APL) by Astolfi et al. in 2021, several similar cases have been reported worldwide. In this report, we present a case of relapsed APL in an adolescent patient, who exhibited the TTMV::RARA fusion gene. This patient exhibited extensive central nervous system involvement and experienced bone marrow necrosis during disease recurrence. Despite achieving complete remission after re-induction chemotherapy, the patient experienced a rapid second relapse, highlighting the extremely aggressive nature of this subtype. These clinical manifestations contribute to the growing recognition of this rare disease.

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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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