一例罕见的费城阳性(P210BCR-ABL1)T 细胞急性淋巴细胞白血病/淋巴瘤病例,强化化疗后仍有极小残留病灶存在

IF 0.7 Q4 HEMATOLOGY
Shruti Shah , Rupayan Kundu , Rahul Mishra , Sudipto Mukherjee , Abhay Singh
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引用次数: 0

摘要

T 细胞急性淋巴细胞白血病/淋巴瘤(T-ALL/LBL)是一种罕见的侵袭性白血病。费城染色体阳性的细胞遗传学异常在 CML 中最为常见。新发 Ph+ T-ALL/LBL 与 CML 的 T 细胞淋巴细胞危象很难区分。我们介绍了一例成人 Ph+ T-ALL/LBL 病例,患者可能有 CML 前驱史。该病例起初被认为是慢性期 CML 病例,但由于诊断上的窘迫而不得不进行淋巴结活检,最终确诊为 Ph+ T-LBL 或 CML 的 T 淋巴细胞增生危象,这种临床表现极为罕见,在我们查阅的文献中也仅有第二例。由于极小残留病(MRD)阳性表明病情凶险,患者接受了一年多的强化化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of Philadelphia-positive (P210BCR-ABL1) T-cell acute lymphoblastic leukemia/lymphoma associated with minimal residual disease persistence after intensive chemotherapeutic approaches

T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) is a rare and aggressive leukemia. Philadelphia chromosome-positive cytogenetic abnormality is most common in CML. It is difficult to differentiate between de novo Ph+ T-ALL/LBL and T-cell lymphoblastic crises of CML. We present a case of adult Ph+ T-ALL/LBL with a likely history of antecedent CML. Initially thought to be a case of chronic-phase CML, a diagnostic quandary led to the pursuit of a lymph node biopsy that established the diagnosis of Ph+ T-LBL or T lymphoblastic blast crisis of CML, a clinical presentation extremely rare and only the second of its kind from our review of the literature. The patient was treated with an intensive chemotherapy regimen for over a year due to persistent minimal residual disease (MRD) positivity indicating aggressive disease.

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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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