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HIV感染背景下伴有11q异常的高级别B细胞淋巴瘤:10例临床病理研究及文献复习

High-grade B-cell lymphoma with 11q aberration in the HIV setting: a clinicopathological study of 10 cases and literature review.

作者信息

Chang Jing, Liang Ying, Gao Yuxue, Wu Menghua, Lv Fudong, Liu Hui, Sun Lin, Yue Zhujun, Meng Lingjia, Zhang Yulin, Jin Mulan

机构信息

Department of Pathology, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Department of Pathology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.

出版信息

Infect Agent Cancer. 2024 Sep 11;19(1):42. doi: 10.1186/s13027-024-00604-4.

Abstract

High-grade B-cell lymphoma with 11q aberration (HGBL-11q) is a distinct lymphoma entity according to the 5th edition of the WHO classification of hematolymphoid tumors. It lacks MYC translocation but carries proximal gains and/or telomeric losses of chromosome 11q. This rare type of B-cell lymphoma is less frequently reported in people living with HIV (PLWH), and its exact frequency remains unclear. Our goal was to retrospectively analyze its frequency in a cohort of aggressive B-cell lymphomas in PLWH, including Burkitt lymphoma (BL, n = 35), diffuse large B-cell lymphoma (DLBCL, n = 48), high-grade B-cell lymphoma, not otherwise specified (HGBL-NOS, n = 13), which was diagnosed as AIDS-related lymphoma (ARL) at our institution. In total, 10/96 (10.4%) cases harbored the typical 11q aberration pattern, predominantly those that had been classified as BL (6/35, 17.1%), DLBCL (2/48, 4.2%), and HGBL, NOS (2/13, 15.4%). We also evaluated 7 cases of AIDS-related HGBL-11q (AR-HGBL-11q) reported in the literature. The median age of our cohort was 35 years, and all the patients were male. Most cases (70%) had a history of HIV infection for over 1 year, and all were involved in lymph nodes (100%), frequently involved extranodal sites (60%), and Ann Arbor stage III/IV. In histomorphology, the cases exhibited diverse cytological features, reminiscent of BL (6 cases), DLBCL (2 cases), and HGBL (2 cases). A comparison of the combined cohort of 17 AR-HGBL-11q cases with 11 ARL cases that lacked both MYC rearrangement and 11q aberration at our institution showed that HGBL-11q cases were characterized by strikingly coarse apoptotic debris (P < 0.001), background rich in eosinophils (P = 0.002), higher expression of the germinal centre marker LMO2 (P = 0.080), lower expression of MUM1 (P = 0.004), BCL2 (P = 0.007), and LEF1 (P = 0.080), and lower positivity for EBER in situ hybridisation (P = 0.027). Notably, one case in our series was EBV-positive, a finding not previously reported in the literature. Furthermore, comparing the prognosis between these two groups, AR-HGBL-11q showed a relatively favorable prognosis (P = 0.15), although the difference was not statistically significant. We analyzed this rare lymphoma entity in the HIV setting and highlighted the importance of integrating histomorphological and immunophenotypic features in its diagnosis and classification.

摘要

根据世界卫生组织血液淋巴系统肿瘤分类第5版,伴有11q异常的高级别B细胞淋巴瘤(HGBL-11q)是一种独特的淋巴瘤实体。它缺乏MYC易位,但存在11号染色体q臂近端增益和/或端粒缺失。这种罕见的B细胞淋巴瘤在HIV感染者(PLWH)中报道较少,其确切发病率尚不清楚。我们的目标是回顾性分析PLWH侵袭性B细胞淋巴瘤队列中HGBL-11q的发病率,包括伯基特淋巴瘤(BL,n = 35)、弥漫性大B细胞淋巴瘤(DLBCL,n = 48)、未另行指定的高级别B细胞淋巴瘤(HGBL-NOS,n = 13),这些病例在我们机构被诊断为艾滋病相关淋巴瘤(ARL)。总共96例中有10例(10.4%)具有典型的11q异常模式,主要是那些被归类为BL(6/35,17.1%)、DLBCL(2/48,4.2%)和HGBL-NOS(2/13,15.4%)的病例。我们还评估了文献中报道的7例艾滋病相关HGBL-11q(AR-HGBL-11q)病例。我们队列的中位年龄为35岁,所有患者均为男性。大多数病例(70%)有超过1年的HIV感染史,所有病例均累及淋巴结(100%),常累及结外部位(60%),Ann Arbor分期为III/IV期。在组织形态学上,这些病例表现出多样的细胞学特征,类似于BL(6例)、DLBCL(2例)和HGBL(2例)。将我们机构17例AR-HGBL-11q病例与11例既无MYC重排也无11q异常的ARL病例的联合队列进行比较,结果显示HGBL-11q病例的特征为凋亡碎片明显粗大(P < 0.001)、背景富含嗜酸性粒细胞(P = 0.002)、生发中心标志物LMO2表达较高(P = 0.080)、MUM1(P = 0.004)、BCL2(P = 0.007)和LEF1(P = 0.080)表达较低,以及EBER原位杂交阳性率较低(P = 0.027)。值得注意的是,我们系列中有1例为EBV阳性,这一发现此前文献中未报道。此外,比较这两组的预后,AR-HGBL-11q显示出相对较好的预后(P = 0.15),尽管差异无统计学意义。我们在HIV背景下分析了这种罕见的淋巴瘤实体,并强调了在其诊断和分类中整合组织形态学和免疫表型特征的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7846/11391791/7cf829804e9a/13027_2024_604_Fig1_HTML.jpg

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