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.
| Item Type: | Journal article |
|---|---|
| Faculties: | Medicine |
| Subjects: | 600 Technology > 610 Medicine and health |
| ISSN: | 1613-5636 |
| Language: | German |
| Item ID: | 78898 |
| Date Deposited: | 15. Dec 2021 14:46 |
| Last Modified: | 15. Dec 2021 14:46 |
