Department of Dermatology, Faculty of Medicine, University of Tokyo, 7-3-1, Hongo, Bunkyo-Ku, Tokyo, 113-8655, Japan.
Acta Derm Venereol. 2014 Jan;94(1):54-7. doi: 10.2340/00015555-1626.
Primary cutaneous follicular helper T (TFH)-cell lymphoma has recently been proposed, and is characterized by proliferation of malignant T cells expressing TFH-cell markers, such as CXCL13, accompanied by numerous reactive B cells. We report here a patient whose skin histology showed massive infiltration of both T and B cells, with a proliferation of arborizing high endothelial venules and follicular dendritic cells. Infiltrating T cells were positive for CXCL13, programmed death (PD)-1, inducible T-cell co-stimulator, and BCL-6. Southern blot analyses using DNA from the skin revealed monoclonality of both T and B cells. The patient had marked resistance to treatments, and complete remission was achieved only after allogeneic stem cell transplantation. The present case showed overlapping features with angio-immunoblastic T-cell lymphoma (AITL), although systemic symptoms were not observed. Further study is needed to define the criteria of this provisional entity, representing the cutaneous counterpart of the nodal follicular peripheral T-cell lymphoma or AITL.
原发性皮肤滤泡辅助 T(TFH)细胞淋巴瘤最近被提出,其特征是表达 TFH 细胞标志物的恶性 T 细胞增殖,如 CXCL13,并伴有大量反应性 B 细胞。我们在此报告一例患者,其皮肤组织学显示大量 T 细胞和 B 细胞浸润,有分枝状高内皮静脉和滤泡树突状细胞增殖。浸润的 T 细胞表达 CXCL13、程序性死亡(PD)-1、诱导性 T 细胞共刺激分子和 BCL-6。使用皮肤 DNA 进行的Southern 印迹分析显示 T 细胞和 B 细胞均具有单克隆性。该患者对治疗有明显的耐药性,仅在异基因干细胞移植后才达到完全缓解。本病例与血管免疫母细胞性 T 细胞淋巴瘤(AITL)具有重叠特征,尽管未观察到全身症状。需要进一步研究来定义这一暂定实体的标准,代表结外滤泡性周围 T 细胞淋巴瘤或 AITL 的皮肤对应物。