毛细胞白血病继发性中枢神经系统受累无转化1例报告并文献复习。

IF 1.7 4区 医学 Q3 HEMATOLOGY
Acta Haematologica Pub Date : 2024-01-01 Epub Date: 2023-11-10 DOI:10.1159/000535066
Kenichi Ito, Kunihiko Harada, Yoshihito Uchino, Kazuhiko Hirano, Naohiro Sekiguchi
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引用次数: 0

摘要

毛细胞白血病(HCL)是一种惰性b细胞淋巴瘤,其特征是特异性基因突变BRAF V600E,影响特异性形态和肿瘤发生。对于HCL,关于继发性中枢神经系统受累(SCNSI)的报道很少。在这里,我们提出的情况下,80岁的妇女谁有复发的HCL与SCNSI。2015年6月,经免疫组化分析鉴定BRAF V600E蛋白,诊断为HCL,并通过化疗免疫治疗控制病情6年。2021年2月,患者因头晕等神经系统症状入院。脑磁共振成像显示大脑异常强化,脑脊液分析显示肿瘤细胞未转化为大细胞。因此,该患者在HCL中被诊断为SCNSI。结论我们报告一例罕见的HCL中SCNSI的临床表现,并进行文献复习。
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 Clinical Case of Secondary Central Nervous System Involvement without Transformation in Hairy Cell Leukemia: A Case Report and Literature Review.

Introduction: Hairy cell leukemia (HCL) is an indolent B-cell lymphoma characterized by a specific genetic mutation, BRAF V600E, which affects the specific morphology and oncogenesis. For HCL, few reports regarding secondary central nervous system involvement (SCNSI) are available. Herein, we present the case of an 80-year-old woman who had a relapse of HCL with SCNSI.

Case presentation: The diagnosis of HCL was made in June 2015 after identifying BRAF V600E proteins by immunohistochemical analysis, and the disease was then controlled for 6 years by employing chemoimmunotherapy. In February 2021, the patient was admitted with neurological symptoms such as dizziness. Magnetic resonance imaging of the brain showed abnormal enhancement in the cerebrum, and cerebrospinal fluid analysis revealed neoplastic cells without transformation into large cells. Thus, the patient was diagnosed as having SCNSI in HCL.

Conclusion: We report a case of a rare clinical presentation of SCNSI in HCL with literature review.

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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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