@article{oai:nagoya.repo.nii.ac.jp:02000161,
 author = {Takahashi Noriyuki and Takeichi Takuya and Nishida Tetsuya and Takahashi Yasuhiro and Sato Juichi and Yamamura Masahiro and Ogi Tomoo and Akiyama Masashi},
 issue = {10},
 journal = {Arthritis & Rheumatology},
 month = {Oct},
 note = {A 55-year-old Japanese man was diagnosed with VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome, which is a newly documented adult-onset autoinflammatory disease caused by somatic UBA1 mutations [1], after four years of symptoms. He had suffered from recurrent fever after the onset of systemic arthralgia, scleritis, periorbital/orbital inflammation, optic perineuritis (A, B, T1-weighted contrast-enhanced magnetic resonance imaging in C and D, arrow in D), and myelodysplastic syndrome., First published: 21 April 2021},
 pages = {1896--1897},
 title = {Extensive multiple organ involvement in VEXAS syndrome},
 volume = {73},
 year = {2021}
}