中枢神经系统alk阴性间变性大细胞淋巴瘤伴IRF4/DUSP22重排。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Brain Tumor Pathology Pub Date : 2022-01-01 Epub Date: 2021-11-18 DOI:10.1007/s10014-021-00415-0
Shino Magaki, Radha Satyadev, Zesheng Chen, Kathryn S Yung, Harry V Vinters, Marsha C Kinney, Jonathan W Said
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引用次数: 2

摘要

间变性大细胞淋巴瘤(ALCL)是一种成熟的t细胞肿瘤,其中大约一半的患者存在ALK基因重排,因此预后良好。最近的研究表明,相当大比例的alk阴性alcl表现出IRF4/DUSP22位点的重排,这也通常与良好的预后相关。原发性累及中枢神经系统(CNS)的ALCL极为罕见。我们报告一例可能是alk阴性ALCL伴IRF4/DUSP22重排累及大脑的病例,患者为55岁男性。磁共振成像显示脑室周围区、胼胝体和扣带回信号异常。活检显示cd30阳性细胞弥漫性实质和血管中心浸润,荧光原位杂交显示IRF4/DUSP22重排。我们还回顾了文献中原发性中枢神经系统alk阴性alcl的临床和病理特征,并强调需要认识到这一实体,以优化适当的管理。
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Central nervous system ALK-negative anaplastic large cell lymphoma with IRF4/DUSP22 rearrangement.

Anaplastic large cell lymphomas (ALCL) are mature T-cell neoplasms, approximately half of which harbor rearrangements of the ALK gene that confer a good prognosis. Recent studies have demonstrated that a significant proportion of ALK-negative ALCLs demonstrate rearrangements of the IRF4/DUSP22 locus that also are typically associated with a favorable prognosis. ALCL with primary involvement of the central nervous system (CNS) is extremely rare. We report what may be the first case of ALK-negative ALCL with IRF4/DUSP22 rearrangement involving the brain in a 55-year-old man. Magnetic resonance imaging demonstrated signal abnormalities in the periventricular region, corpus callosum and cingulate gyrus. Biopsy revealed a diffuse parenchymal and angiocentric infiltrate of CD30-positive cells that showed IRF4/DUSP22 rearrangement by fluorescence in situ hybridization. We also review the clinical and pathologic features of primary CNS ALK-negative ALCLs in the literature and highlight the need for awareness of this entity to optimize appropriate management.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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