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华氏巨球蛋白血症的中枢神经系统受累:一项基于人群的宾-尼尔综合征与组织学转化的比较研究。

Central nervous system involvement in Waldenström macroglobulinemia: a comparative population-based study of Bing-Neel syndrome and histological transformation.

作者信息

Østergaard Simon, Munksgaard Lars, Hammer Troels, Nielsen Torsten Holm, Pedersen Mette Ølgod, Gjerdrum Lise Mette Rahbek

机构信息

Department of Pathology, Copenhagen University Hospital - Zealand University Hospital Roskilde, Roskilde, Denmark.

Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

出版信息

Ann Hematol. 2025 Feb;104(2):1007-1014. doi: 10.1007/s00277-025-06194-4. Epub 2025 Jan 24.

Abstract

Central nervous system (CNS) involvement in Waldenström macroglobulinemia (WM) is a rare complication that can manifest as Bing-Neel syndrome (BNS) or as histological transformation (HT) to diffuse large B-cell lymphoma (DLBCL). We report data from a single-center cohort of 469 patients consecutively diagnosed with WM between 2000 and 2022. BNS was identified in 1.5% (n = 7) and HT with CNS involvement (CNS-HT) in 1.7% (n = 8) of patients. The cumulative incidence of BNS and CNS-HT at 15 years was 2.6% and 2.7%, respectively, with CNS-HT more likely to develop in closer proximity to the initial WM diagnosis. One patient with CNS-HT exhibited a preceding phase of BNS before transformation. In general, patients with BNS and CNS-HT presented with diverse neurological symptoms and clinical features. Parenchymal lesions were uniformly found in all patients with CNS-HT, while neuroimaging findings were less consistent in patients with BNS. Involvement of multiple extramedullary sites was observed in approximately half of the patients with both BNS and CNS-HT. Patients with CNS-HT had poor outcomes, with a median overall survival of 10 months following the onset of CNS involvement, whereas BNS was associated with a more favorable prognosis, particularly in patients treated with ibrutinib. This study is the first to present a comparative analysis of BNS and CNS-HT in WM, providing novel insights into their incidence, clinical features, and outcomes.

摘要

中枢神经系统(CNS)受累于华氏巨球蛋白血症(WM)是一种罕见的并发症,可表现为宾-尼尔综合征(BNS)或组织学转化为弥漫性大B细胞淋巴瘤(DLBCL)的组织学转化(HT)。我们报告了2000年至2022年间连续诊断为WM的469例单中心队列患者的数据。1.5%(n = 7)的患者被诊断为BNS,1.7%(n = 8)的患者被诊断为伴有CNS受累的HT(CNS-HT)。15年时BNS和CNS-HT的累积发病率分别为2.6%和2.7%,CNS-HT更有可能在初次诊断WM后不久发生。1例CNS-HT患者在转化前出现了BNS的前期阶段。总体而言,BNS和CNS-HT患者表现出多样的神经症状和临床特征。所有CNS-HT患者均发现有实质病变,而BNS患者的神经影像学表现则不太一致。在大约一半的BNS和CNS-HT患者中观察到多个髓外部位受累。CNS-HT患者预后较差,CNS受累后中位总生存期为10个月,而BNS的预后则较好,尤其是在接受伊布替尼治疗的患者中。本研究首次对WM中的BNS和CNS-HT进行了比较分析,为它们的发病率、临床特征和预后提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/11971055/f8cd1db169c9/277_2025_6194_Fig1_HTML.jpg

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