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Published on: May 16, 2025
Clinical features of juvenile lupus erythematosus in Iranian children
M H Moradinejad1, G R Zamani, A R Kiani
1Dep. of Rheumatology, Medical Sciences, University of Tehran, Tehran, Iran. swt_f@yahoo.com
Insights
Juvenile Systemic Lupus Erythematosus (JSLE) presents with diverse and severe clinical features, frequently involving skin, musculoskeletal, and renal systems. Early diagnosis is crucial for managing this complex pediatric autoimmune disease.
Area of Science:
- Pediatric Rheumatology
- Autoimmune Diseases
- Clinical Immunology
Background:
- Juvenile Systemic Lupus Erythematosus (JSLE) is a chronic autoimmune disease affecting children.
- Understanding the clinical spectrum of JSLE is essential for timely diagnosis and management.
- Previous studies highlight the variability in JSLE presentation and outcomes.
Purpose of the Study:
- To analyze the clinical and laboratory features of childhood-onset Systemic Lupus Erythematosus (JSLE).
- To describe the diverse organ involvement and severity in pediatric SLE patients.
- To contribute to a better understanding of JSLE for improved diagnostic strategies.
Main Methods:
- Retrospective multicenter study including 45 children diagnosed with JSLE before age 16.
- Patients met the American College of Rheumatology (ACR) 1982 revised criteria for SLE.
- Data collected on clinical manifestations, laboratory findings, and outcomes.
Main Results:
- The female to male ratio was 8:1, with a mean age of onset at 10.5 years.
- Common manifestations included skin (88.8%), musculoskeletal (77.7%), and renal (64.4%) involvement.
- Significant rates of hematological (55.5%), cardiovascular (26%), central nervous system (17%), and pulmonary (11%) disease were observed.
Conclusions:
- JSLE exhibits diverse and often severe clinical manifestations in children.
- Early recognition and diagnosis are critical for managing JSLE.
- Further multicenter studies in varied geographic regions are needed to enhance understanding and diagnosis of JSLE.
Objective:
Analysis of the clinical and laboratory features of childhood onset systemic lupus erythematosus (JSLE).
Patients And Method:
Forty five children, aged below 16, were enrolled in this retrospective multicenter study. All patients fulfilled the American College of Rheumatology revised criteria 1982 for the diagnosis of SLE and had shown clinical manifestations of the disease before the age of 16.
Results:
The female to male ratio was 8:1. The mean age at onset was 10.5 (ranged between 3 and 16 years). Thirty patients (66%) were correctly diagnosed before referring to our Center. The clinical manifestation in different organs were as follows: 40 patients (88.8%) had skin involvement, 35 patients (77.7%) experienced musculoskeletal involvement, 29 children (64.4%) suffered from renal disease, hematological abnormalities were detected in 25 patients (55.5%), 12 patients (26%) had cardiovascular disease, 10 patients (17%) presented central nervous system involvement, and 5 patients (11%) experienced SLE-related pulmonary disease. During the follow up period, four patients died, two from renal failure, one from CNS complications of JSLE, and one due to severe sepsis.
Conclusion:
Clinical manifestations of Juvenile SLE are diverse and often severe. Similar studies should be undertaken in different geographic areas in order to provide a good insight of the disease towards a correct diagnosis of JSLE.
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