医学
结节性多动脉炎
复发性多软骨炎
病理
多发性骨髓瘤
巨细胞动脉炎
疾病
皮肤病科
血管炎
内科学
作者
Alexandre Fagart,T. Quéméneur,Guillaume Collet,F. Demailly,Clémentine Rousselin
标识
DOI:10.1097/rlu.0000000000004443
摘要
VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is an adult-onset autoinflammatory disease caused by somatic UBA1 mutations first described in 2020. Most of these patients met clinical criteria for an inflammatory syndrome (relapsing polychondritis, Sweet syndrome, polyarteritis nodosa, or giant-cell arteritis) or a hematologic condition (myelodysplastic syndrome or multiple myeloma) or both. We described here an FDG PET/CT "leopard man" appearance, with abnormal marrow recruitment the findings, in a 70-year-old man diagnosed with a VEXAS syndrome.
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