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Peripheral T cell lymphoma-associated hemophagocytic syndrome in a patient with human adjuvant disease

机译:患有人类辅助疾病的患者的外周血T细胞淋巴瘤相关的噬血细胞综合征

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摘要

Hemophagocytic syndrome (HPS) is a rare complication of lymphoma. We report a 70-year-old woman with human adjuvant disease who developed lymphoma-associated HPS (LAHPS) and elevated serum soluble interleukin (IL)-2 receptor. Despite intensive therapy, she died of pneumonia. Necropsy revealed a prominent spleen containing atypical T cells and many erythrophagocytizing histiocytes.
机译:噬血细胞综合征(HPS)是一种罕见的淋巴瘤并发症。我们报告一位患有人类辅助疾病的70岁妇女,该妇女发展了淋巴瘤相关的HPS(LAHPS)和血清可溶性白介素(IL)-2受体升高。尽管进行了强化治疗,她还是死于肺炎。尸检显示突出的脾脏,其中包含非典型的T细胞和许多吞噬红细胞的组织细胞。

著录项

  • 来源
    《Rheumatology International》 |2003年第3期|143-145|共3页
  • 作者单位

    Division of Rheumatology and Clinical Immunology First Department of Internal Medicine Showa University School of Medicine;

    Division of Rheumatology and Clinical Immunology First Department of Internal Medicine Showa University School of Medicine;

    Division of Rheumatology and Clinical Immunology First Department of Internal Medicine Showa University School of Medicine;

    Division of Rheumatology and Clinical Immunology First Department of Internal Medicine Showa University School of Medicine;

    Department of Allergy and Immunological Disease Metropolitan Komagome Hospital;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Hemophagocytic syndrome; Human adjuvant disease; Peripheral T cell lymphoma;

    机译:吞噬细胞综合征;人类辅助疾病;外周T细胞淋巴瘤;

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