Lefèvre Guillaume, Copin Marie-Christine, Roumier Christophe, Aubert Hélène, Avenel-Audran Martine, Grardel Nathalie, Poulain Stéphanie, Staumont-Sallé Delphine, Seneschal Julien, Salles Gilles, Ghomari Kamel, Terriou Louis, Leclech Christian, Morati-Hafsaoui Chafika, Morschhauser Franck, Lambotte Olivier, Ackerman Félix, Trauet Jacques, Geffroy Sandrine, Dumezy Florent, Capron Monique, Roche-Lestienne Catherine, Taieb Alain, Hatron Pierre-Yves, Dubucquoi Sylvain, Hachulla Eric, Prin Lionel, Labalette Myriam, Launay David, Preudhomme Claude, Kahn Jean-Emmanuel
Institute of Immunology, French Eosinophil Network and Research Unit EA2686, Lille University Hospital, Université Lille Nord de France, Lille Department of Internal Medicine - Clinical Immunology Unit and Research Unit EA2686, Lille University Hospital, Université Lille Nord de France, Lille
Institute of Pathology and CNRS Unit Research UMR 8161, Lille University Hospital, Université Lille Nord de France, Lille.
Haematologica. 2015 Aug;100(8):1086-95. doi: 10.3324/haematol.2014.118042. Epub 2015 Feb 14.
The CD3(-)CD4(+) lymphoid variant of hypereosinophilic syndrome is characterized by hypereosinophilia and clonal circulating CD3(-)CD4(+) T cells. Peripheral T-cell lymphoma has been described during this disease course, and we observed in our cohort of 23 patients 2 cases of angio-immunoblastic T-cell lymphoma. We focus here on histopathological (n=12 patients) and immunophenotypic (n=15) characteristics of CD3(-)CD4(+) lymphoid variant of hypereosinophilic syndrome. Atypical CD4(+) T cells lymphoid infiltrates were found in 10 of 12 CD3(-)CD4(+) L-HES patients, in lymph nodes (n=4 of 4 patients), in skin (n=9 of 9) and other extra-nodal tissues (gut, lacrymal gland, synovium). Lymph nodes displayed infiltrates limited to the interfollicular areas or even an effacement of nodal architecture, associated with proliferation of arborizing high endothelial venules and increased follicular dendritic cell meshwork. Analysis of 2 fresh skin samples confirmed the presence of CD3(-)CD4(+) T cells. Clonal T cells were detected in at least one tissue in 8 patients, including lymph nodes (n=4 of 4): the same clonal T cells were detected in blood and in at least one biopsy, with a maximum delay of 23 years between samples. In the majority of cases, circulating CD3(-)CD4(+) T cells were CD2(hi) (n=9 of 14), CD5(hi) (n=12 of 14), and CD7(-)(n=4 of 14) or CD7(low) (n=10 of 14). Angio-immunoblastic T-cell lymphoma can also present with CD3(-)CD4(+) T cells; despite other common histopathological and immunophenotypic features, CD10 expression and follicular helper T-cell markers were not detected in lymphoid variant of hypereosinophilic syndrome patients, except in both patients who developed angio-immunoblastic T-cell lymphoma, and only at T-cell lymphoma diagnosis. Taken together, persistence of tissular clonal T cells and histopathological features define CD3(-)CD4(+) lymphoid variant of hypereosinophilic syndrome as a peripheral indolent clonal T-cell lymphoproliferative disorder, which should not be confused with angio-immunoblastic T-cell lymphoma.
高嗜酸性粒细胞综合征的CD3(-)CD4(+)淋巴细胞变异型的特征为嗜酸性粒细胞增多和克隆性循环CD3(-)CD4(+) T细胞。在该疾病过程中曾有外周T细胞淋巴瘤的报道,在我们的23例患者队列中,我们观察到2例血管免疫母细胞性T细胞淋巴瘤。我们在此聚焦于高嗜酸性粒细胞综合征CD3(-)CD4(+)淋巴细胞变异型的组织病理学(n = 12例患者)和免疫表型(n = 15例)特征。在12例CD3(-)CD4(+) L - HES患者中的10例发现非典型CD4(+) T细胞淋巴浸润,见于淋巴结(4例患者中的4例)、皮肤(9例中的9例)和其他结外组织(肠道、泪腺、滑膜)。淋巴结显示浸润局限于滤泡间区,甚至淋巴结结构消失,伴有树枝状高内皮小静脉增生和滤泡树突状细胞网络增加。对2份新鲜皮肤样本的分析证实存在CD3(-)CD4(+) T细胞。8例患者的至少一个组织中检测到克隆性T细胞,包括淋巴结(4例中的4例):在血液和至少一次活检中检测到相同的克隆性T细胞,样本之间的最大间隔时间为23年。在大多数病例中,循环CD3(-)CD4(+) T细胞为CD2(高表达)(14例中的9例)、CD5(高表达)(14例中的12例),以及CD7(-)(14例中的4例)或CD7(低表达)(14例中的10例)。血管免疫母细胞性T细胞淋巴瘤也可出现CD3(-)CD4(+) T细胞;尽管有其他常见的组织病理学和免疫表型特征,但在高嗜酸性粒细胞综合征淋巴细胞变异型患者中未检测到CD10表达和滤泡辅助性T细胞标志物,仅在发生血管免疫母细胞性T细胞淋巴瘤的2例患者中,且仅在T细胞淋巴瘤诊断时检测到。综上所述,组织克隆性T细胞的持续存在和组织病理学特征将高嗜酸性粒细胞综合征的CD3(-)CD4(+)淋巴细胞变异型定义为一种外周惰性克隆性T细胞淋巴增殖性疾病,不应与血管免疫母细胞性T细胞淋巴瘤相混淆。