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Updated: Jul 27, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
[Adult-onset Still's disease : Rare adult-onset autoinflammatory syndrome]
E Oms1, M Tronnier2
1Klinik für Dermatologie, Allergologie und Venerologie, Helios Klinikum Hildesheim GmbH, Senator-Braun-Allee 33, 31135, Hildesheim, Deutschland. elisabeth.oms@helios-gesundheit.de.
Abstract:
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease characterized by high spiking fever, arthritis, salmon-pink maculopapular rash and multiple organ involvement. We report a case of an adult-onset Still's disease that meets Yamaguchi's criteria and presented with typical clinical manifestations. AOSD is treated with anti-inflammatory medications. Standard therapy includes corticosteroids. Other medications like azathioprine, methotrexate or interleukin-1 or -6 blockers can be used when standard steroid treatment is not adequate.
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