A clinical phenotype of VEXAS syndrome with pleural effusion, infiltrates, and systemic inflammation in a 76-year-old patient: a case report-Reference-Cited by-同舟云学术

A clinical phenotype of VEXAS syndrome with pleural effusion, infiltrates, and systemic inflammation in a 76-year-old patient: a case report

Published:2024-08-24 Issue:1 Volume:18 Page:
ISSN:1752-1947
Container-title:Journal of Medical Case Reports
language:en
Short-container-title:J Med Case Reports

Author:

Berger Melanie,Schumacher Falk,Wollsching-Strobel Maximilian,Kroppen Doreen,Stanzel Sarah B.,Majorski Daniel S.,Fricke Kathrin,Plath Ilka,Windisch Wolfram,Zimmermann Maximilian^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1186/s13256-024-04688-9.pdf

Reference15 articles.

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2. Beck DB, Bodian DL, Shah V, et al. Estimated prevalence and clinical manifestations of UBA1 variants associated with VEXAS syndrome in a clinical population. JAMA. 2023;329:318–24. https://doi.org/10.1001/jama.2022.24836.

3. Beck DB, Werner A, Kastner DL, et al. Disorders of ubiquitylation: unchained inflammation. Nat Rev Rheumatol. 2022;18:435–47. https://doi.org/10.1038/s41584-022-00778-4.

4. Aksentijevich I, Zhou Q. NF-κB pathway in autoinflammatory diseases: dysregulation of protein modifications by ubiquitin defines a new category of autoinflammatory diseases. Front Immunol. 2017;8:399. https://doi.org/10.3389/fimmu.2017.00399.

5. Touitou I, Aksentijevich I. Genetic approach to the diagnosis of autoinflammatory diseases. In: Hashkes PJ, Laxer RM, Simon A, editors. Textbook of autoinflammation. Cham: Springer International Publishing; 2019. p. 225–37.