Literature DB >> 35986821

Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome (VEXAS syndrome) with prominent supraglottic larynx involvement: a case-based review.

Camila Andrea Guerrero-Bermúdez1, Andrés Felipe Cardona-Cardona2, Edwin Jesús Ariza-Parra3, Juan Ignacio Arostegui4, Anna Mensa-Vilaro4, Jordi Yague4, Gloria Vásquez5, Carlos Horacio Muñoz-Vahos5,6,7.   

Abstract

Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome (VEXAS syndrome) is a recently described genetic disorder that gathers autoinflammatory symptoms and myeloid dysplasia. The first description was reported in 2020, and subsequently, a growing number of cases have been described worldwide. Herein, we describe a case of a 72-year-old male patient with VEXAS syndrome with p.Met41Val mutation of the UBA1 gene, prominent supraglottic larynx involvement, and costochondritis. To our knowledge, this is the first report of VEXAS syndrome in Colombia and South America. This disease could present features of relapsing polychondritis, polyarteritis nodosa, giant cell arteritis, and Sweet syndrome, associated with hematologic involvement, including cytopenias, myelodysplastic syndrome, or thromboembolic disease. Supraglottic larynx chondritis and costochondritis are atypical manifestations. These features were proposed previously to differentiate relapsing polychondritis from VEXAS syndrome but are not entirely reliable like in the case described. A diagnosis of VEXAS should be considered in male patients with incomplete or complete features of the previously described conditions, refractory to treatment, requiring high-dose glucocorticoids, and associated progressive hematologic abnormalities. Key Points • VEXAS syndrome is a recently described genetic (somatic mutations in UBA1 gene) disorder that gathers autoinflammatory and hematologic manifestations. • VEXAS syndrome should be considered in male patients with incomplete or complete features of relapsing polychondritis, polyarteritis nodosa, giant cell arteritis, and Sweet syndrome, refractory to treatment, associated with hematologic involvement, including cytopenias, myelodysplastic syndrome, or thromboembolic disease. • Glucocorticoids ameliorate symptoms effectively. However, other treatment options are limited due to a lack of evidence. Traditional immunosuppressants and biological therapy have been used empirically with limited efficacy and a transient effect. Bone marrow transplant offers a curative approach, but it has high morbidity and mortality.
© 2022. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).

Entities:  

Keywords:  Myelodysplastic syndromes; Polyarteritis nodosa; Relapsing polychondritis; VEXAS syndrome; Vasculitis

Mesh:

Substances:

Year:  2022        PMID: 35986821     DOI: 10.1007/s10067-022-06338-1

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   3.650


  19 in total

Review 1.  Genetics of somatic auto-inflammatory disorders.

Authors:  James A Poulter; Sinisa Savic
Journal:  Semin Hematol       Date:  2021-10-09       Impact factor: 3.851

2.  Toward a pathophysiology inspired treatment of VEXAS syndrome.

Authors:  Maël Heiblig; Bhavisha A Patel; Emma M Groarke; Estelle Bourbon; Pierre Sujobert
Journal:  Semin Hematol       Date:  2021-10-05       Impact factor: 3.851

Review 3.  VEXAS within the spectrum of rheumatologic disease.

Authors:  Matthew J Koster; Kenneth J Warrington
Journal:  Semin Hematol       Date:  2021-10-09       Impact factor: 3.851

4.  Correction to: "Living with COVID"-implications for immunosuppressed and immunocompromised.

Authors:  A Nune; K P Iyengar; R Botchu; Bhupen Barman; C Manzo
Journal:  Clin Rheumatol       Date:  2022-11       Impact factor: 3.650

Review 5.  VEXAS syndrome.

Authors:  Peter C Grayson; Bhavisha A Patel; Neal S Young
Journal:  Blood       Date:  2021-07-01       Impact factor: 25.476

6.  VEXAS syndrome in a female patient with constitutional 45,X (Turner syndrome).

Authors:  Ryan J Stubbins; Eric McGinnis; Bhupinder Johal; Luke Yc Chen; Lorena Wilson; Daniela Ospina Cardona; Thomas J Nevill
Journal:  Haematologica       Date:  2022-04-01       Impact factor: 9.941

7.  Innovations in genomics for undiagnosed diseases: vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome.

Authors:  Ryan J Stubbins; Hannah Cherniawsky; Luke Y C Chen; Thomas J Nevill
Journal:  CMAJ       Date:  2022-04-11       Impact factor: 8.262

8.  Novel somatic mutations in UBA1 as a cause of VEXAS syndrome.

Authors:  James A Poulter; Jason C Collins; Catherine Cargo; Ruth M De Tute; Paul Evans; Daniela Ospina Cardona; David T Bowen; Joanna R Cunnington; Elaine Baguley; Mark Quinn; Michael Green; Dennis McGonagle; David B Beck; Achim Werner; Sinisa Savic
Journal:  Blood       Date:  2021-07-01       Impact factor: 25.476

9.  Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease.

Authors:  David B Beck; Marcela A Ferrada; Keith A Sikora; Amanda K Ombrello; Jason C Collins; Wuhong Pei; Nicholas Balanda; Daron L Ross; Daniela Ospina Cardona; Zhijie Wu; Bhavisha Patel; Kalpana Manthiram; Emma M Groarke; Fernanda Gutierrez-Rodrigues; Patrycja Hoffmann; Sofia Rosenzweig; Shuichiro Nakabo; Laura W Dillon; Christopher S Hourigan; Wanxia L Tsai; Sarthak Gupta; Carmelo Carmona-Rivera; Anthony J Asmar; Lisha Xu; Hirotsugu Oda; Wendy Goodspeed; Karyl S Barron; Michele Nehrebecky; Anne Jones; Ryan S Laird; Natalie Deuitch; Dorota Rowczenio; Emily Rominger; Kristina V Wells; Chyi-Chia R Lee; Weixin Wang; Megan Trick; James Mullikin; Gustaf Wigerblad; Stephen Brooks; Stefania Dell'Orso; Zuoming Deng; Jae J Chae; Alina Dulau-Florea; May C V Malicdan; Danica Novacic; Robert A Colbert; Mariana J Kaplan; Massimo Gadina; Sinisa Savic; Helen J Lachmann; Mones Abu-Asab; Benjamin D Solomon; Kyle Retterer; William A Gahl; Shawn M Burgess; Ivona Aksentijevich; Neal S Young; Katherine R Calvo; Achim Werner; Daniel L Kastner; Peter C Grayson
Journal:  N Engl J Med       Date:  2020-10-27       Impact factor: 91.245

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