Journals / Zeynep Kamil Tıp Bülteni / 2026 / Cilt: 36 Sayı: 2

A case of juvenil dermatomyositis

Jüvenil dermatomitozitli bir olgu sunumu

Pages
93–96
Publication Date
2005-03-01
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AI Summary & Key Takeaways

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

Since our case was 16 months, we wanted to consider that JDM may be seen at smaller ages, too.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Juvenile dermatomyositis (JDM), the most common of the pediatric inflammatory myopathies, is a systemic vasculopathy with characteristic cutaneous findings and focal areas of myositis resulting in progressive proximal muscle weakness that is responsive to the prompt institution of immunosuppressive therapy.
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Key Findings & Data:JDM is mostly seen between the ages of 5-14 years of age.
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Conclusion & Impact:Since our case was 16 months, we wanted to consider that JDM may be seen at smaller ages, too.
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Dermatomiyozit · Kas hastalıkları · Vaskülit

Abstract

Juvenile dermatomyositis (JDM), the most common of the pediatric inflammatory myopathies, is a systemic vasculopathy with characteristic cutaneous findings and focal areas of myositis resulting in progressive proximal muscle weakness that is responsive to the prompt institution of immunosuppressive therapy. JDM is mostly seen between the ages of 5-14 years of age. Since our case was 16 months, we wanted to consider that JDM may be seen at smaller ages, too.

Özet

Jüvenil Dermatomiyozit (JDM); pediatrik miyopatilerin en yaygını olup, deri bulguları ve progresif olarak proksimal kaslarda zayıflığa yol açan, fokal miyozitlerle seyreden ve immünsupresif tedaviye cevap veren sistemik bir vaskülopatidir. En sık 5-14 yaşlar arasında görülür. 16 aylık bir olguyu yaşının küçük olması nedeniyle sunmak istedik.

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Cite This Article

Giray, T., Cantürk, Ö., Ağzıkuru, T., Erdağ, G. Ç., Çiçek, N., Akın, Y., Vitrinel, A. (2005). A case of juvenil dermatomyositis. Zeynep Kamil Tıp Bülteni, Cilt: 36 Sayı: 2, 93–96. https://doi.org/10.16948/zktb.47333

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References (9)

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