一例以血细胞减少为首发表现的难治性机化性肺炎合并复发性多软骨炎，诊断为VEXAS综合征：7年病程 - Suppr | 超能文献

相似文献

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A Case of polychondritis-onset refractory organizing pneumonia with cytopaenia diagnosed as VEXAS syndrome: the disease course of 7 years.一例以血细胞减少为首发表现的难治性机化性肺炎合并复发性多软骨炎，诊断为VEXAS综合征：7年病程

Rheumatology (Oxford). 2021 Oct 2;60(10):e356-e359. doi: 10.1093/rheumatology/keab349.

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Vacuoles in neutrophil precursors in VEXAS syndrome: diagnostic performances and threshold.VEXAS综合征中性粒细胞前体中的空泡：诊断效能与阈值

Br J Haematol. 2021 Oct;195(2):286-289. doi: 10.1111/bjh.17679. Epub 2021 Aug 2.

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A Case of VEXAS Syndrome Complicated by Hemophagocytic Lymphohistiocytosis.1例伴有噬血细胞性淋巴组织细胞增生症的VEXAS综合征病例。

J Clin Immunol. 2021 Oct;41(7):1648-1651. doi: 10.1007/s10875-021-01070-y. Epub 2021 Jun 2.

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Case Report: Genetic Double Strike: VEXAS and TET2-Positive Myelodysplastic Syndrome in a Patient With Long-Standing Refractory Autoinflammatory Disease.病例报告：遗传性双重打击：长期难治性自身炎症性疾病患者的 VEXAS 和 TET2 阳性骨髓增生异常综合征。

Front Immunol. 2022 Jan 20;12:800149. doi: 10.3389/fimmu.2021.800149. eCollection 2021.

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UBA1 and DNMT3A mutations in VEXAS syndrome. A case report and literature review.VEXAS综合征中的UBA1和DNMT3A突变：一例报告及文献综述

Mod Rheumatol Case Rep. 2022 Jan 7;6(1):134-139. doi: 10.1093/mrcr/rxab021.

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Clinical characteristics, disease trajectories and management of vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome: a systematic review.空泡、E1 酶、X 连锁、自身炎症、体细胞（VEXAS）综合征的临床特征、疾病轨迹和治疗：系统评价。

Rheumatol Int. 2024 Jul;44(7):1219-1232. doi: 10.1007/s00296-023-05513-0. Epub 2023 Dec 21.

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Somatic Mutations in and Severe Adult-Onset Autoinflammatory Disease.和严重成人发病的自身炎症性疾病中的体细胞突变。

N Engl J Med. 2020 Dec 31;383(27):2628-2638. doi: 10.1056/NEJMoa2026834. Epub 2020 Oct 27.

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Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS.UBA1 体细胞突变导致的成人发作性自身炎症：荷兰 VEXAS 患者的病例系列。

J Allergy Clin Immunol. 2022 Jan;149(1):432-439.e4. doi: 10.1016/j.jaci.2021.05.014. Epub 2021 May 25.

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Looking beyond VEXAS: Coexistence of undifferentiated systemic autoinflammatory disease and myelodysplastic syndrome.超越VEXAS综合征：未分化的系统性自身炎症性疾病与骨髓增生异常综合征并存

Semin Hematol. 2021 Oct;58(4):247-253. doi: 10.1053/j.seminhematol.2021.10.003. Epub 2021 Oct 9.

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[Orbitopathy and bilateral posterior scleritis in VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome].VEXAS（空泡、E1酶、X连锁、自身炎症性、体细胞）综合征中的眼眶病和双侧后巩膜炎

J Fr Ophtalmol. 2024 Sep;47(7):104151. doi: 10.1016/j.jfo.2024.104151. Epub 2024 Mar 19.

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1

dysfunction in VEXAS and cancer.VEXAS 相关功能障碍与癌症。

Oncotarget. 2024 Sep 30;15:644-658. doi: 10.18632/oncotarget.28646.

2

The role of FDG-PET imaging in VEXAS syndrome: a multicentric case series and a systematic review of the literature.FDG-PET 成像在 VEXAS 综合征中的作用：一项多中心病例系列研究和文献系统评价。

Intern Emerg Med. 2024 Nov;19(8):2331-2345. doi: 10.1007/s11739-024-03763-9. Epub 2024 Sep 9.

3

Successful treatment with fludarabine and cyclophosphamide in a VEXAS syndrome patient with associated myelodysplastic syndrome: a case report and systematic review.