Systemic pulse steroid therapy, antibiotics, and antihypertensive and anticonvulsive drugs were given.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:A 10-year-old boy with epidermolysis bullosa simplex (Weber-Cockayne variant) together with leukocytoclastic vasculitis is presented.
📊
Key Findings & Data:He was admitted to the hospital with the provisional diagnoses of infected epidermolysis bullosa simplex or drug eruption.
💡
Conclusion & Impact:Systemic pulse steroid therapy, antibiotics, and antihypertensive and anticonvulsive drugs were given.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
A 10-year-old boy with epidermolysis bullosa simplex (Weber-Cockayne variant) together with leukocytoclastic vasculitis is presented. He was admitted to the hospital with the provisional diagnoses of infected epidermolysis bullosa simplex or drug eruption. On the sixth day of hospitalization he developed palpable purpura, abdominal pain and bloody diarrhea, together with hematuria and proteinuria. A generalized tonic-clonic convulsion, changes in mental status, fluctuations in arterial blood pressure and intractable pain in his extremities occurred during the course of hospitalization. Systemic pulse steroid therapy, antibiotics, and antihypertensive and anticonvulsive drugs were given. On the 30
🔖
Cite This Article
BÜYÜKKALE, G., BAKKALOĞLU, A., SEÇMEER, G., KANRA, G., CEYHAN, M., SEZGİN, G. (2022). Leukocytoclastic vasculitis in a child with epidermolysis bullosa simplex. Turkish Journal of Pediatrics, Cilt: 41 - Sayı: 2, 277–282. https://ajindex.com/articles/613487