<scp>VEXAS</scp> Syndrome: A Case Series From a <scp>Single‐Center</scp> Cohort of Italian Patients With Vasculitis
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- Francesco Muratore
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Chiara Marvisi
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia, Reggio Emilia, Italy, and Università di Modena e Reggio Emilia Modena Italy
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- Paola Castrignanò
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia, Reggio Emilia, Italy, and Università di Modena e Reggio Emilia Modena Italy
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- Davide Nicoli
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Enrico Farnetti
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Orsola Bonanno
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Rosina Longo
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Piera Zaldini
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Elena Galli
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia, Reggio Emilia, Italy, and Università di Modena e Reggio Emilia Modena Italy
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- Nicholas Balanda
- National Human Genome Research Institute NIH Bethesda Maryland
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- David B. Beck
- National Human Genome Research Institute NIH Bethesda Maryland
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- Peter C. Grayson
- National Institute of Arthritis and Musculoskeletal and Skin Diseases NIH Bethesda Maryland
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- Nicolò Pipitone
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Luigi Boiardi
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia Reggio Emilia Italy
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- Carlo Salvarani
- Azienda Unità Sanitaria Locale‐IRCCS di Reggio Emilia, Reggio Emilia, Italy, and Università di Modena e Reggio Emilia Modena Italy
書誌事項
- 公開日
- 2022-03-03
- 権利情報
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- http://creativecommons.org/licenses/by-nc-nd/4.0/
- DOI
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- 10.1002/art.41992
- 公開者
- Wiley
この論文をさがす
説明
<jats:sec><jats:title>Objective</jats:title><jats:p>To identify patients with VEXAS syndrome (vacuoles, E1 enzyme, X‐linked, autoinflammatory, somatic syndrome) from a single‐center cohort of Italian patients with vasculitis, using a clinically oriented phenotype‐first approach.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We retrospectively reviewed the clinical records of 147 consecutive male patients followed up in our vasculitis clinic from 2013 to date. All patients with a diagnosis of vasculitis and treatment‐resistant manifestations of inflammation, persistently elevated inflammation markers, and hematologic abnormalities were identified. Bone marrow aspirates were examined for the presence of vacuoles. Sequencing of ubiquitin‐activating enzyme E1 (UBA‐1) was performed using genomic DNA from peripheral blood leukocytes or bone marrow tissue.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Seven patients with vasculitis and concomitant features of VEXAS syndrome were identified. A final diagnosis of VEXAS syndrome was made in 3 of the 5 patients who underwent sequencing of UBA‐1 (diagnosis was made postmortem for 1 patient). In all 3 patients, examination of the bone marrow aspirate revealed vacuoles characteristic of VEXAS syndrome, and all 3 patients met the definitive World Health Organization criteria for myelodysplastic syndrome. Cytogenetic analysis showed normal karyotypes in all 3 patients.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>To our knowledge, this is the first report of VEXAS syndrome associated with antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis. Our data emphasize the need to consider VEXAS syndrome when evaluating patients with various forms of systemic vasculitis. The novel association between VEXAS syndrome and ANCA‐associated vasculitis reported herein warrants further investigation.</jats:p></jats:sec>
収録刊行物
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- Arthritis & Rheumatology
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Arthritis & Rheumatology 74 (4), 665-670, 2022-03-03
Wiley