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Updated: Aug 8, 2026

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The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
Coexistent linear scleroderma and juvenile systemic lupus erythematosus
M Majeed1, S M Al-Mayouf, E Al-Sabban
1Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Pediatric Dermatology
|December 21, 2000
Summary
This case study details a girl initially diagnosed with linear scleroderma who later developed systemic lupus erythematosus (SLE). It reviews prior instances of this dual diagnosis in pediatric patients.
Area of Science:
- Pediatric Rheumatology
- Dermatology
- Immunology
Background:
- Linear scleroderma is a localized connective tissue disease.
- Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder.
- Co-occurrence of these conditions is rare, particularly in childhood.
Observation:
- A pediatric patient initially presented with linear scleroderma.
- Over a five-year period, the patient subsequently developed features of SLE.
- This progression highlights a potential link between the two autoimmune conditions.
Findings:
- The case demonstrates a sequential development of systemic lupus erythematosus following an initial diagnosis of linear scleroderma in a child.
- Review of existing literature indicates limited but documented instances of this combined presentation.
- This suggests a possible shared autoimmune pathway or progression from localized to systemic disease.
Implications:
- Understanding the relationship between linear scleroderma and SLE is crucial for early diagnosis and management in pediatric cases.
- Further research into the underlying mechanisms may reveal novel therapeutic targets for both conditions.
- This case underscores the importance of long-term monitoring for autoimmune manifestations in children with localized scleroderma.
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