Qubaja Marwan, Audouin Josée, Moulin Jean Claude, Molina Thierry Jo, Le Tourneau Agnès, Gaulard Philippe, Straub Pierre, Audhuy Bruno, Diebold Jacques
Service d'anatomie et de cytologie pathologiques, Hôtel-Dieu, 75181 Paris Cedex 04, France.
Hum Pathol. 2009 Feb;40(2):264-9. doi: 10.1016/j.humpath.2008.05.018. Epub 2008 Aug 28.
We report the case of a 62-year-old patient presenting with 3 different patterns of follicular helper T-cell lymphoma. The patient initially presented with angioimmunoblastic T-cell lymphoma. A nodal relapse in the form of follicular T-cell lymphoma with a progressively transformed germinal center pattern occurred 8 years later. Two years later, this was followed by another relapse presenting as a predominantly large-cell peripheral T-cell lymphoma, unspecified. All neoplastic cells expressed CD3, CD5, and CD2, with some neoplastic cells also expressing CD7. These cells also expressed CD4, with some expressing CD10, bcl-6, CXCL13, and programmed death-1, all of which are characteristic of the normal subset of follicular T-helper cells. The immunophenotype showed a progressive increase in the proportion of cells expressing CD10, bcl-6, CXCL13, and programmed death-1 from the first to the last lymphoma. In addition, neoplastic T cells from the last biopsy sample expressed CD20.
我们报告了一例62岁的患者,其呈现出3种不同模式的滤泡辅助性T细胞淋巴瘤。该患者最初表现为血管免疫母细胞性T细胞淋巴瘤。8年后,出现了以滤泡性T细胞淋巴瘤形式的淋巴结复发,伴有进行性转化的生发中心模式。两年后,又出现了另一次复发,表现为主要为未特指的大细胞外周T细胞淋巴瘤。所有肿瘤细胞均表达CD3、CD5和CD2,部分肿瘤细胞还表达CD7。这些细胞也表达CD4,部分表达CD10、bcl-6、CXCL13和程序性死亡-1,所有这些都是正常滤泡辅助性T细胞亚群的特征。免疫表型显示,从第一次淋巴瘤到最后一次淋巴瘤,表达CD10、bcl-6、CXCL13和程序性死亡-1的细胞比例逐渐增加。此外,最后一次活检样本中的肿瘤性T细胞表达CD20。