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Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
Lea-Sophie Stahl1,2, Ann-Christin Wolters3, Ocko Kautz4
1Abteilung für experimentelle Allergologie und Immundermatologie, Carl von Ossietzky Universität Oldenburg, Oldenburg, Deutschland.
A misdiagnosed case of granuloma annulare was reclassified as Wells' syndrome (eosinophilic cellulitis) after a decade of unsuccessful treatment. Systemic pulse steroid therapy achieved complete remission, highlighting its efficacy for this rare skin condition.
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