[血管内大 B 细胞淋巴瘤的临床病理特征和五例碰撞瘤】。]

Q3 Medicine
J Liu, G Z Liu, L Xia, H Y Wang, X F Zhang, H Liu
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引用次数: 0

摘要

目的研究血管内大 B 细胞淋巴瘤(IVLBCL)及其碰撞肿瘤的临床病理特征、诊断和鉴别诊断。方法收集5例IVLBCL病例,其中2例为碰撞瘤,1例并发肝硬化。对其形态学和免疫表型进行了分析。回顾相关文献。结果2例女性,3例男性,年龄在53至73岁之间,中位年龄为65岁。肿瘤分别位于下肢、右侧小脑半球、左肾、双侧鼻腔和肝脏。病例 2 和病例 3 分别是在脑膜瘤和肾细胞癌组织中偶然发现的。病例 5 有肝硬化背景。形态学上,非典型大淋巴细胞位于小血管和毛细血管腔内,细胞质少,色素沉着,核仁突出,有明显的有丝分裂。免疫组化结果显示,IVLBCL 肿瘤细胞表达 CD20 和 PAX5,其中 2 例为 CD5 阳性。5例中有1例为GCB表型,4例为非GCB表型。所有病例均表达C-MYC(阳性率为10%-40%)。4例PD-L1阳性(阳性率为60%-90%)。Ki-67增殖指数为70%-90%。CKpan、CD3、TDT和CD34均为阴性。在病例2中,脑膜瘤细胞的PR、EMA和波形蛋白呈阳性,但CKpan和PD-L1呈阴性。在病例3中,肾癌细胞的CKpan、PAX8、EMA、波形蛋白、CAⅨ和CD10呈阳性,而PD-L1呈阴性。5例患者均未检测到EBER表达(原位杂交)或C-MYC基因易位(FISH,断裂探针)。对 3 例患者进行了随访,所有患者均在 1-13 个月内死亡。结论:IVLBCL是一种侵袭性很强的淋巴瘤,临床表现隐匿,预后较差。IVLBCL的碰撞肿瘤极为罕见。更好地了解IVLBCL有助于病理学家避免误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinicopathological features of intravascular large B-cell lymphoma and collision tumors of five cases].

Objective: To investigate the clinicopathological characteristics, diagnosis and differential diagnosis of intravascular large B-cell lymphoma (IVLBCL) and its collision tumors. Methods: Five cases of IVLBCL were collected, including 2 cases of collision tumors, and 1 case complicated with liver cirrhosis. The morphology and immunophenotype were analyzed. The related literature was reviewed. Results: There were 2 females and 3 males, aged from 53 to 73 years, with a median age of 65 years. The tumors were located in the lower extremities, right cerebellar hemisphere, left kidney, bilateral nasal cavity, and liver, respectively. Cases 2 and 3 were incidentally found in meningioma and renal cell carcinoma tissues, respectively. Case 5 had a background of liver cirrhosis. Morphologically, atypical large lymphoid cells were located in small blood vessels and capillary lumen, with little cytoplasm, hyperchromasia, prominent nucleoli, and obvious mitotic figures. Immunohistochemically, the IVLBCL tumor cells expressed CD20 and PAX5; 2 cases were CD5 positive. One of the 5 cases was GCB phenotype, and 4 cases were non-GCB phenotype. All cases expressed C-MYC (positive rate was 10%-40%). PD-L1 was positive in 4 cases (positive rate was 60%-90%). Ki-67 proliferation index was 70%-90%. CKpan, CD3, TDT, and CD34 were negative. In case 2, meningioma cells were positive for PR, EMA, and vimentin, but negative for CKpan and PD-L1. In case 3, renal carcinoma cells were positive for CKpan, PAX8, EMA, vimentin, CAⅨ and CD10, while PD-L1 was negative. No EBER expression (by in situ hybridization) or C-MYC gene translocation (FISH, break-apart probe) was detected in any of the 5 cases. Three patients were followed up, and all died within 1-13 months. Conclusions: IVLBCL is a highly aggressive lymphoma, with occult clinical manifestations and poor prognosis. Collision tumors of IVLBCL are extremely rare. A better understanding of IVLBCL would help pathologists avoid misdiagnoses.

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中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
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10377
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