Author(s)

Ibrahim Abdulaziz Hamama^1,2,3*, Tariq Alhazmi^2,3, Waseemoddin Patel¹

¹Division of Neonatology, Department of Pediatrics, King Abdullah Bin Abdulaziz University Hospital, Princess Nora Bint Abdulrahman University, Riyadh, Saudi Arabia.
²Department of Pediatrics, AlNoor Specialist Hospital, Mecca, Saudi Arabia.
³Department of Pediatrics, Maternity and Children Hospital, Mecca, Saudi Arabia.

Background: Infantile myofibromatosis is an uncommon disorder characterized by multiple fibromatous tumours involving skin, bone, muscle, viscera and subcutaneous tissue. It is a rare benign mesenchymal tumour; most commonly occurs in infancy or early childhood. The clinical presentation can mimic malignant tumours of infancy or childhood. Case Presentation: We describe a rare case of multicentric Infantile myofibromatosis in a 6-month-old infant presenting with multiple scalp swellings and associated skeletal abnormalities (adducted thumbs, clinodactyly and bilateral hallux valgus deformity of great toes). The case required surgical excision of all scalp lesions and orthopedic manipulation of skeletal abnormalities. Conclusion: Infantile myofibromatosis presenting as multiple lesions in the scalp associated with skeletal abnormalities, is very rare. To best of our knowledge, the unique combination of the distinct skeletal abnormalities in infantile myofibromatosis has not been reported so far. This report emphasizes the possibility of skeletal abnormalities in infantile myofibromatosis.

Infantile Myofibromatosis, Multiple Fibromatous, Skeletal Abnormalities, Clinodactyly, Hallux Valgus Deformity

Hamama, I. , Alhazmi, T. and Patel, W. (2020) Multiple Infantile Myofibromatosis with Skeletal Abnormalities. Health, 12, 849-856. doi: 10.4236/health.2020.127062.