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Familial tumoral calcinosis
Amal Alkhatib1, Laura E Burton2, Robert Carachi3
1Consultant Paediatric Surgeon, Department of Paediatric Surgery, Khartoum Teaching Hospital, Sudan Consultant Paediatric Surgeon, Department of Paediatric Surgery, Latifa Hospital, Dubai, United Arab Emirates.
Introduction:
Tumoral calcinosis is a rare condition characterised by progressive, ectopic, periarticular deposits of calcium. These tumour-like growths often infiltrate muscle and tendon, usually presenting as multiple masses or as a painless, solitary mass. Our case report will focus on familial tumoral calcinosis, an autosomal recessive metabolic disorder generally observed in patients within the first two decades of life.
Case Presentation:
Our case report introduces two Sudanese siblings from consanguineous parents who presented with simultaneous recurrent multiple soft tissue swellings.
Conclusion:
The cases discussed highlight the main features of familial tumoral calcinosis and indicate the need for improved clinical guidance on the investigations, treatment and genetic screening of familial tumoral calcinosis.
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