VEXAS syndrome: A new mimicker of idiopathic multicentric Castleman disease

•Only two cases of VEXAS with Castleman-like lymph node mimicking iMCD are reported in the literature.•VEXAS syndrome should be considered in the presence of iMCD suspicion, including patients with compatible histology. Idiopathic Multicentric Castleman Disease (iMCD) is a complex and poorly underst...

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Veröffentlicht in:	Joint, bone, spine : revue du rhumatisme bone, spine : revue du rhumatisme, 2024-07, Vol.91 (4), p.105731, Article 105731
Hauptverfasser:	Philip, Rémi, Cadro, Vincent, Aouba, Achille, Chantepie, Sylvain, Bracquemart, Claire, Dumont, Anaël
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Autoinflammatory disease Castleman Disease - diagnosis Castleman Disease - genetics Diagnosis, Differential Humans Idiopathic multicentric Castleman disease Lymph Nodes - pathology Male Middle Aged Multicentric Castleman disease Mutation Syndrome Ubiquitin-Activating Enzymes - genetics VEXAS syndrome
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