Online ISSN: 2149-3189
2015
Monthly
Nicaea Medical Publishing
Türkiye

Solitary myofibroma in children: a report of two cases

Çağrı Coşkun, Kemal Kösemehmetoğlu, Mehmet Ayvaz, İbrahim Vargel, Üstün Aydıngöz, Hatice Nursun Özcan, Ali Varan, Bilgehan Yalçın
DOI
https://doi.org/10.18621/eurj.1382704
Abstract
Myofibromas are rare benign tumors of myofibroblasts, seen more commonly in children. These tumors typically involve soft tissues with a predilection for the head and neck. Malignant neoplasia is often suspected for these rapidly growing tumors in early childhood. Clinical and radiological findings are not typical, and histopathological examination makes the definitive diagnosis. This pathology requires the intervention of a multidisciplinary team and regular follow-up. We report our experience with two children with myofibromas, one in the right arm of a 5-year-old girl and the other in the right axilla of a 9-year-old boy. Tumors were totally resected in both children, who are under follow-up with no adjuvant treatment free of disease after surgery. Myofibroma should be considered in the differential diagnosis of pediatric soft tissue tumors. Surgical resection is sufficient for treatment and patients should be followed regularly for possible recurrences.
Keywords
Solitary myofibroma, arm, axilla, immunohistochemistry, surgery
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How to Cite
1.
Coşkun Çağrı, Kösemehmetoğlu K, Ayvaz M, et al. Solitary myofibroma in children: a report of two cases. Eur Res J. 2024;10(3):333-337. doi:10.18621/eurj.1382704
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Vol. 10 No. 3 (2024)

Article Information

  • Article Type Case Report
  • Submitted February 21, 2026
  • Published May 3, 2024
  • Issue Vol. 10 No. 3 (2024)
  • Section Case Report
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