Keywords
Juvenile dermatomyositis
Plain radiography
Pediatric rheumatology
Soft tissue calcification
Categories
How to Cite
Abstract
Calcinosis universalis is a rare and debilitating complication of juvenile dermatomyositis (JDM), characterized by extensive deposition of calcium salts in soft tissues. This case study presents a 12-year-old female patient with a known history of JDM who developed widespread calcinosis, documented through plain radiographic imaging. X-ray evaluation revealed diffuse sheet-like and nodular calcifications involving multiple soft tissue regions, correlating with the patient’s progressive musculoskeletal pain, reduced mobility, and recurrent skin ulcerations. Clinical correlations highlighted the significant impact of calcinosis on functional outcomes, disease morbidity, and quality of life. The discussion emphasizes the role of conventional radiography in identifying and monitoring the extent of calcinosis, while also considering therapeutic challenges and the limited effectiveness of available interventions. This case underscores the importance of early recognition, multidisciplinary management, and further research into targeted therapies to reduce disease burden in affected pediatric populations.
References
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Copyright (c) 2026 Maxwell Adu , Mahama Bukari , Felicia Philipa Aggrey , Jacob Leonard Ago, Abdul Rashid Karim