AI Summary & Key Takeaways
AI InsightWe described an ashmatic patient in whom Churg-Strauss syndrome with skin eruptions developed within six months after the withdrawal of systemic corticosteroids in association with leucocytoclastic vasculitis as well as eosinophilia, paranasal sinusitis and pulmonary infiltration.
📌 3 Key Takeaways
Abstract
Churg-Strauss syndrome is a rare disorder characterized by hypereosinophilia and systemic vasculitis occuring in individuals with asthma and allergic rhinitis. We described an ashmatic patient in whom Churg-Strauss syndrome with skin eruptions developed within six months after the withdrawal of systemic corticosteroids in association with leucocytoclastic vasculitis as well as eosinophilia, paranasal sinusitis and pulmonary infiltration.
Özet
Churg-Strauss sendromu astma ve allerjik rinitle birlikte görülen hipereozinofili ve sistemik vaskülitle karakterize nadir bir hastalıktır. Biz astma nedeniyle sistemik kortikosteroid tedavisi alan bir olguda steroid kesilmesinden yaklaşık 6 ay sonra deri döküntüleri ile başvuran ve lökositoklastik vaskülitin yanı sıra eozinofili, paranasal sinüzit ve pulmoner infiltrasyon saptanan Churg Strauss sendromlu bir olguyu sunuyoruz.