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VEXAS 综合征的诊断和治疗方法:临床怀疑的重要性和甲氨蝶呤的应用。

Approaches for the diagnosis and treatment of VEXAS syndrome: the importance of clinical suspicion and the use of methotrexate.

机构信息

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.

Rheumatology and Clinical Immunology, IRCCS Humanitas Research Hospital, Rozzano, Italy.

出版信息

Ann Hematol. 2024 Nov;103(11):4789-4791. doi: 10.1007/s00277-024-05863-0. Epub 2024 Aug 23.

Abstract

Vacuoles, E1-enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) syndrome is caused by mutations in the UBA1 gene in myeloid precursors, leading to systemic inflammatory manifestations. We present the case of a 75-year-old man presenting with fever, panniculitis, and macrocytic anemia testing repeatedly negative for UBA1 mutations in peripheral blood samples, but ultimately found positive on bone marrow mononuclear cell DNA. The man has been successfully treated with prednisone and methotrexate.

摘要

空泡性表皮松解症样包涵体肌病(VEXAS)综合征是由髓系前体细胞中 UBA1 基因突变引起的,导致全身炎症表现。我们报告了一例 75 岁男性病例,该患者表现为发热、脂膜炎和巨红细胞性贫血,在外周血样本中反复检测 UBA1 突变均为阴性,但最终在骨髓单核细胞 DNA 中检测为阳性。该患者经泼尼松和甲氨蝶呤治疗后病情得到缓解。

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