Juvenile dermatomyositis, clinical manifestations and outcome in an Iranian cohort
المؤلفون المشاركون
Rezaieyazdi, Zahrah
Saghafi, Masud
Hashimzadah, Kamila
المصدر
Egyptian Pediatric Association Gazette
العدد
المجلد 62، العدد 2 (30 يونيو/حزيران 2014)، ص ص. 46-51، 6ص.
الناشر
تاريخ النشر
2014-06-30
دولة النشر
مصر
عدد الصفحات
6
التخصصات الرئيسية
الموضوعات
الملخص EN
Objective : Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy of childhood and is characterized by proximal muscle weakness and pathognomonic skin rashes.
In this study, we performed a descriptive cross sectional study to assess the clinical manifestations and outcomes of 39 patients with JDM from the northeast of Iran during 12 years and compared our findings with other studies.
Design : 39 patients (16 boys and 23 girls) with juvenile dermatomyositis were studied retrospectively between 2001 and 2013.
Gender, age at disease onset and diagnosis, clinical manifestations, laboratory data at onset, treatment and outcome of these patients were reviewed.
Measurements and results : The mean age of onset was 9.42 ± 3.85 years.
At the time of presentation, muscle weakness occurred in 100 % ; heliotrope rash in 51.2 % ; gottron’s papules in 46.1 %, calcinosis in 12.8 %, and 87.1 % had at least one abnormal muscle enzyme result.
Muscle biopsy was performed in 15.3 % and was abnormal in all.
All patients received corticosteroids ; but methotrexate, hydroxychloroquine, intravenous immunoglobulin, or azathioprine was added to corticosteroid in some patients.
The mean follow-up period was 22.66 ± 23.53 months.
Conclusions : This study was in parallel with other reviews except for calcinosis which was observed with lower frequency.
It is suggested that delay in diagnosis and treatment may be associated with calcinosis.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Saghafi, Masud& Rezaieyazdi, Zahrah& Hashimzadah, Kamila. 2014. Juvenile dermatomyositis, clinical manifestations and outcome in an Iranian cohort. Egyptian Pediatric Association Gazette،Vol. 62, no. 2, pp.46-51.
https://search.emarefa.net/detail/BIM-442749
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Saghafi, Masud…[et al.]. Juvenile dermatomyositis, clinical manifestations and outcome in an Iranian cohort. Egyptian Pediatric Association Gazette Vol. 62, no. 2 (2014), pp.46-51.
https://search.emarefa.net/detail/BIM-442749
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Saghafi, Masud& Rezaieyazdi, Zahrah& Hashimzadah, Kamila. Juvenile dermatomyositis, clinical manifestations and outcome in an Iranian cohort. Egyptian Pediatric Association Gazette. 2014. Vol. 62, no. 2, pp.46-51.
https://search.emarefa.net/detail/BIM-442749
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references : p. 50-51
رقم السجل
BIM-442749
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
تقوم هذه الخدمة بالتحقق من التشابه أو الانتحال في الأبحاث والمقالات العلمية والأطروحات الجامعية والكتب والأبحاث باللغة العربية، وتحديد درجة التشابه أو أصالة الأعمال البحثية وحماية ملكيتها الفكرية. تعرف اكثر