通过多种检测方式检测到一种新型 BCR::ABL1 变异体。

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2024-08-16 eCollection Date: 2024-01-01 DOI:10.1155/2024/8486267
J Jean, M Sukhanova, D Dittmann, J Gao, L J Jennings
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引用次数: 0

摘要

慢性髓性白血病(CML)与导致不同 BCR::ABL1 融合转录本的几个断点区有关。这些断点区包括主要断点区(M-BCR)、次要断点区(m-BCR)和μ断点区(u-BCR),分别对应 p210、p190 和 p230 融合转录本。该患者为 38 岁女性,新诊断为慢性期 CML。通过定性反转录聚合酶链反应和毛细管电泳,检测到一个新的 p210 融合转录本剪接变体。随后进行的 FISH 研究显示,BCR::ABL1 融合的阳性率为 86.5%。定量实时聚合酶链反应(PCR)显示 p210 融合转录本为阴性。桑格测序进一步确定了该变异体的特征。该变异体位于框架内,预计具有功能性。该病例说明,需要结合不同的检测技术来全面鉴定罕见的 BCR::ABL1 融合转录本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel BCR::ABL1 Variant Detected with Multiple Testing Modalities.

Chronic myeloid leukemia (CML) is associated with several breakpoint regions that result in different BCR::ABL1 fusion transcripts. These include the major breakpoint region (M-BCR), minor breakpoint region (m-BCR), and mu breakpoint region (u-BCR) corresponding to p210, p190, and p230 fusion transcripts, respectively. This patient is a 38-year-old female with a new diagnosis of CML in chronic phase. A novel p210 fusion transcript splice variant was detected with qualitative reverse transcription PCR and capillary electrophoresis. Subsequent FISH study was performed, which revealed 86.5% positive for the BCR::ABL1 fusion. Quantitative real-time polymerase chain reaction (PCR) showed a negative result for the p210 fusion transcript. The variant was further characterized by Sanger sequencing. This variant is in-frame and predicted to be functional. This case illustrates the need for a combination of different testing techniques to fully characterize the rare BCR::ABL1 fusion transcripts.

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