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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3096286114

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

About this item

Full title

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

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

Journal title

Annals of hematology, 2024-11, Vol.103 (11), p.4789-4791

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

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 pe...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_3096286114

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3096286114

Other Identifiers

ISSN

0939-5555,1432-0584

E-ISSN

1432-0584

DOI

10.1007/s00277-024-05863-0

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