Suppr超能文献

系统性红斑狼疮巨噬细胞活化综合征后严重骨髓再生障碍

Severe Bone Marrow Aplasia Following Macrophage Activation Syndrome in Systemic Lupus Erythematosus.

作者信息

Ichimura Hirona, Ichikawa Satoshi, Ono Koya, Inokura Kyoko, Hoshi Yosuke, Shirai Tsuyoshi, Fukuhara Noriko, Yokoyama Hisayuki, Fujii Hiroshi, Harigae Hideo

机构信息

Department of Hematology, Tohoku University Hospital.

Department of Rheumatology, Tohoku University Hospital.

出版信息

Tohoku J Exp Med. 2023 Aug 11;260(4):301-304. doi: 10.1620/tjem.2023.J037. Epub 2023 May 11.

Abstract

Macrophage activation syndrome (MAS) is a potentially fatal complication of rheumatic diseases, characterized by activated macrophages with hemophagocytosis and multiple organ damage. We report a case of MAS associated with systemic lupus erythematosus that initially presented with severe liver dysfunction. Although it was improved with steroids and plasmapheresis, severe pancytopenia was subsequently experienced, and the bone marrow showed severe aplasia similar to aplastic anemia. Nevertheless, the administration of immunosuppressants resulted in the recovery of blood counts within two weeks. When severe MAS results in cytokine overproduction, bone marrow aplasia may occur, for which immunosuppressive therapy may be highly effective.

摘要

巨噬细胞活化综合征(MAS)是风湿性疾病的一种潜在致命并发症,其特征为活化的巨噬细胞伴噬血细胞现象和多器官损害。我们报告一例与系统性红斑狼疮相关的MAS病例,该病例最初表现为严重肝功能障碍。尽管使用类固醇和血浆置换后病情有所改善,但随后出现了严重全血细胞减少,骨髓显示出与再生障碍性贫血相似的严重发育不全。然而,给予免疫抑制剂后,血细胞计数在两周内恢复。当严重的MAS导致细胞因子过度产生时,可能会发生骨髓发育不全,对此免疫抑制治疗可能非常有效。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验