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伴有显著肉芽肿反应的经典型霍奇金淋巴瘤:20例临床病理研究

Classic Hodgkin lymphoma with marked granulomatous reaction: A clinicopathologic study of 20 cases.

作者信息

Xu Jie, Li Shaoying, Yin C Cameron, Patel Keyur P, Tang Guilin, Wang Wei, Miranda Roberto N, Garces Sofia, Tang Zhenya, Lin Pei, Medeiros L Jeffrey

机构信息

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.

出版信息

Hum Pathol. 2023 Apr;134:114-123. doi: 10.1016/j.humpath.2022.12.014. Epub 2022 Dec 28.

Abstract

Granulomatous reactions can be associated with various types of lymphoma, most commonly classic Hodgkin lymphoma (CHL). In some cases, the granulomatous reaction is extensive, obscuring the presence of neoplastic cells and potentially leading to delayed diagnosis and treatment. It is unknown if this subgroup of CHL has any unique clinicopathologic features. Here, we assessed the clinical and pathological features of 20 cases of CHL with a marked granulomatous reaction, defined in this study as granulomas representing ≥50% of the total cellularity/space of the specimen. This cohort of patients showed a male predominance (M:F ratio = 1.9:1) and 75% of patients were older than 40 years. Nineteen (95%) patients presented with lymphadenopathy with the neck/supraclavicular areas being most commonly involved (11/19; 58%). Advanced stage (III-IV) disease and B symptoms were present in 69% and 64% of patients, respectively. The morphologic features of these neoplasms fit best with mixed cellularity type. The Hodgkin and Reed-Sternberg (HRS) cells were positive for CD30, PAX5 (weak), pSTAT3 (80%), CD15 (70%), PD-L1 (67%), EBV-encoded small RNA (EBER)/LMP1 (50%) and CD20 (42%), and were negative for CD3, CD5, CD45, ALK and pERK. The histiocytes of the granulomas were positive for PD-L1 (67%), pSTAT3 (50%), and were negative for pERK and cyclin D1. Next generation sequencing using a 162-gene panel was negative for mutations in 4 cases. With a median follow-up of 58.9 months (range, 3.4-199.2 months), the median overall survival was 111 months and the 5-year overall survival was 78%. In summary, patients with CHL and a marked granulomatous reaction can present a diagnostic challenge and the pathologist must be alert to the possible presence of CHL to avert potential misdiagnosis. The histiocytes in the granulomas frequently express PD-L1, likely through the activation of the JAK/STAT pathway, suggesting a potential role for PD-1 blockade therapy in these patients.

摘要

肉芽肿反应可与多种类型的淋巴瘤相关,最常见的是经典型霍奇金淋巴瘤(CHL)。在某些情况下,肉芽肿反应广泛,掩盖了肿瘤细胞的存在,可能导致诊断和治疗延迟。目前尚不清楚这一亚组CHL是否具有任何独特的临床病理特征。在此,我们评估了20例具有明显肉芽肿反应的CHL的临床和病理特征,本研究将其定义为肉芽肿占标本总细胞数/空间的≥50%。这组患者以男性为主(男:女比例 = 1.9:1),75%的患者年龄超过40岁。19例(95%)患者出现淋巴结病,最常累及颈部/锁骨上区域(11/19;58%)。分别有69%和64%的患者处于晚期(III-IV期)疾病且有B症状。这些肿瘤的形态学特征最符合混合细胞型。霍奇金和里德-斯腾伯格(HRS)细胞CD30、PAX5(弱阳性)、pSTAT3(80%)、CD15(70%)、PD-L1(67%)、EBV编码的小RNA(EBER)/LMP1(50%)和CD20(42%)呈阳性,而CD3、CD5、CD45、ALK和pERK呈阴性。肉芽肿的组织细胞PD-L1(67%)、pSTAT3(50%)呈阳性,pERK和细胞周期蛋白D1呈阴性。使用162个基因的面板进行的二代测序在4例中未发现突变。中位随访时间为58.9个月(范围3.4 - 199.2个月),中位总生存期为111个月,5年总生存率为78%。总之,患有CHL且有明显肉芽肿反应的患者可能带来诊断挑战,病理学家必须警惕CHL的可能存在以避免潜在的误诊。肉芽肿中的组织细胞经常表达PD-L1,可能是通过JAK/STAT途径的激活,提示PD-1阻断疗法在这些患者中可能发挥作用。

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