Journals / The Journal of Pediatric Research / 2016 / Cilt: 3 - Sayı: 2

Livedoid Vasculopathy with Behçet Disease

Behçet Hastalığı ile Birlikte Görülen Livedoid Vaskülopati

Pages
120–122
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

By analyzing the case mentioned above, a rarely encountered vasculitis form of Behçet disease has been emphasized.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Livedoid vasculopathy is a rarely encountered disease.
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Key Findings & Data:A 15-year-old girl presented with painful ulcerations, porcelain-white atrophic scars of the malleolar region and dorsal aspect of the feet, livedo reticularis on the limbs.
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Conclusion & Impact:By analyzing the case mentioned above, a rarely encountered vasculitis form of Behçet disease has been emphasized.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Livedoid vasculopathy is a rarely encountered disease. A 15-year-old girl presented with painful ulcerations, porcelain-white atrophic scars of the malleolar region and dorsal aspect of the feet, livedo reticularis on the limbs. Arthralgia was an accompanying complaint and she was overwhelmed by oral ulcers and folliculitis. Also she had family history for Behçet disease. By analyzing the case mentioned above, a rarely encountered vasculitis form of Behçet disease has been emphasized.

Özet

Livedoid vaskülopati nadir görülen bir hastalıktır. On beş yaşında kız hasta malleolar bölge ve ayak dorsalinde bulunan porselensi-beyaz atrofik skarlar, ağrılı ülserle livedo retikülaris kliniğine sahipti. Artralji, oral ülserler ve follikülit eşlik eden diğer bulgulardı. Ailede Behçet hastalığı öyküsü vardı. Bu olgu ile Behçet hastalığının nadir bir vaskülit formunun vurgulanması amaçlandı.

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Cite This Article

VATANSEVER, Z., PAÇ, A. K., SÖZERİ, B., GÜNDÜZ, Z., DÜŞÜNSEL, R., POYRAZOĞLU, H., DENİZ, K. (2016). Livedoid Vasculopathy with Behçet Disease. The Journal of Pediatric Research, Cilt: 3 - Sayı: 2, 120–122. https://ajindex.com/articles/362845

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