Familial tumoral calcinosis

Author:

Alkhatib Amal12,Burton Laura E3,Carachi Robert4

Affiliation:

1. Consultant Paediatric Surgeon, Department of Paediatric Surgery, Khartoum Teaching Hospital, Sudan

2. Consultant Paediatric Surgeon, Department of Paediatric Surgery, Latifa Hospital, Dubai, United Arab Emirates

3. Medical Student, School of Medicine, University of Glasgow, UK

4. Professor of Surgical Paediatrics, Department of Surgical Paediatrics, Royal Hospital for Sick Children, UK

Abstract

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.

Publisher

SAGE Publications

Subject

General Medicine

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