Abstract
We describe a 15-year-old girl with eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome, CSS). Under steroid treatment there was a rapid regression of hemoptysis. Termination of steroid therapy could not be achieved after a 7-month follow-up. Previously, the girl had suffered for a long time from therapy refractive bronchial asthma, which in CSS is typically associated with blood eosinophilia. A cardiac or neurological manifestation is particularly dangerous with a high rate of mortality in the generalization phase. Systemic steroid therapy, if necessary with immunosuppressive agents, has become established as an effective therapeutic option.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Medizin |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
ISSN: | 1613-5636 |
Sprache: | Deutsch |
Dokumenten ID: | 78898 |
Datum der Veröffentlichung auf Open Access LMU: | 15. Dez. 2021, 14:46 |
Letzte Änderungen: | 15. Dez. 2021, 14:46 |