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Chronic active Epstein-Barr virus infection with progression to large granular lymphocytic leukemia

机译:慢性活动性爱泼斯坦-巴尔病毒感染,进展为大颗粒性淋巴细胞白血病

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Dear Editor,A 34-year-old woman presented with 1-year history of recurrent vesicles, papules and erosions on her face (Fig. 1). Skin biopsy showed diffuse infiltration of lymphocytes and plasma cells with epidermal necrosis (Fig. 2a,b). Hypersensitivity to mosquito bites was not observed. We first diagnosed severe hydroa vacciniforme in an adult and performed further examination. Laboratory examination showed leukocytosis (white blood cell [WBC], 23 000L) with 20% granular lymphocytes. Flow cytometric analysis of peripheral blood mononuclear cells showed abnormal increment of CD3+ CD8+ cells (CD3+ 88.6%, CD3+CD4+ 36.1%, CD3+CD8+ 44.1%) which were considered as increased large granular lymphocytes (LGL) in laboratory examination. The immunophenotype of LGL was CD3+CD8+CD16-CD56-.
机译:尊敬的编辑,一位34岁的女性,她的脸上出现了1年的反复性囊泡,丘疹和糜烂的病史(图1)。皮肤活检显示淋巴细胞和浆细胞弥漫性浸润,并伴有表皮坏死(图2a,b)。没有观察到对蚊虫叮咬的超敏反应。我们首先在成人中诊断出严重的水痘疫苗,并进行了进一步检查。实验室检查显示白细胞增多症(白细胞[WBC],23 000 / nL)含20%颗粒淋巴细胞。外周血单核细胞的流式细胞仪分析显示,CD3 + CD8 +细胞异常增加(CD3 + 88.6%,CD3 + CD4 + 36.1%,CD3 + CD8 + 44.1%),在实验室检查中被认为是大颗粒淋巴细胞(LGL)增加。 LGL的免疫表型为CD3 + CD8 + CD16-CD56-。

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