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Multilokuläres Pyoderma gangraenosum: Assoziation mit der Erstmanifestation einer primär biliären Cholangitis

A 16-year-old female patient with previously diagnosed acne vulgaris was transferred to our clinic in reduced general condition with rapidly progressive and extremely painful ulcerations. In the laboratory exam, inflammatory parameters were highly elevated, but she was normothermic. Based on the fin...

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Detalles Bibliográficos
Autores principales: Kögel, Julian, Berneburg, Mark, Karrer, Sigrid, Drexler, Konstantin, Niebel, Dennis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290030/
https://www.ncbi.nlm.nih.gov/pubmed/37326669
http://dx.doi.org/10.1007/s00105-023-05161-2
Descripción
Sumario:A 16-year-old female patient with previously diagnosed acne vulgaris was transferred to our clinic in reduced general condition with rapidly progressive and extremely painful ulcerations. In the laboratory exam, inflammatory parameters were highly elevated, but she was normothermic. Based on the findings, we diagnosed multilocular pyoderma gangrenosum. Further investigations established the diagnosis of primary biliary cholangitis as the underlying condition. Treatment with systemic corticosteroids was initiated and we started therapy with ursodeoxycholic acid. This led to improvement within a few days. PAPA-syndrome (pyogenic arthritis, pyoderma gangrenosum and acne vulgaris) could be ruled out by genetic analysis.