T细胞非霍奇金淋巴瘤临床明显嗜酸性细胞增多1例

C. Agrawal, K. Das, S. Verma, N. Shirazi, Mansi Kala
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引用次数: 0

摘要

本研究描述了一个高嗜酸性粒细胞的病例,他表现出明显的高嗜酸性粒细胞的表现,并检测到有潜在的非霍奇金淋巴瘤。男性患者表现为深度虚弱和多个非瘙痒结节性皮肤病变2周。皮肤结节活检显示异常淋巴细胞沉积。淋巴结活检示单核异常细胞消失,CD4和5阳性,细胞角蛋白和CD20阴性。他被诊断为T-NHL。[图3a,图3b] NHL细胞累及骨髓。他的复视和头痛反应鞘内甲氨蝶呤和可能累及中枢神经系统的疾病被考虑。由于临床进展,家庭选择退出对抗疗法治疗计划。他后来死于疾病进展。本病例显示了临床明显嗜酸性细胞增多症与T - NHL之间罕见而有趣的联系。该研究提示,嗜酸性粒细胞过多的病例应彻底评估T细胞疾病。病例报告Agrawal等;中国生物医学杂志,9(1):1-5,2019;文章no.IBRR。45392 2
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overt Clinical Hypereosinophilia in T- cell Non Hodgkin Lymphoma: A Case Report
The study describes a case of hyper-eosinophilia who was presented with overt manifestation of high eosinophil and detected to have underlying non Hodgkin lymphoma. The male patient was presented with profound weakness and multiple non itchy nodular skin lesion for 2 weeks. Biopsy from skin nodule showed deposits of abnormal lymphocytes. Lymph node biopsy showed effacement with mono nuclear abnormal cells which showed positivity for CD4 and 5, negative for cytokeratin and CD20. He was diagnosed to have T-NHL. [Fig. 3a, Fig. 3b] Bone marrow showed involvement by NHL cells. His diplopia and headache responded to intra-thecal methotrexate and possibly CNS involvement of disease was considered. Family opted out of allopathic treatment plan due to clinical progression. He later died of disease progression. This case illustrates the rare and interesting association of overt clinical hyper-eosinophilia and T NHL. The study suggests that cases with hyper eosinophilia should be evaluated thoroughly for T cell disease. Case Report Agrawal et al.; IBRR, 9(1): 1-5, 2019; Article no.IBRR.45392 2
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