Myositis ossificans in the pediatric population: a systematic scoping review.

biopsy child diagnosis imaging myositis ossificans

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2023
Historique:
received: 15 09 2023
accepted: 13 11 2023
medline: 2 1 2024
pubmed: 2 1 2024
entrez: 1 1 2024
Statut: epublish

Résumé

Circumscribed or pseudomalignant myositis ossificans (MO) is a rare and benign condition characterized by heterotopic bone formation in soft tissues. The clinical presentation of MO, imaging investigations, histological findings, and treatment strategies are unclear, especially in the pediatric population. A literature search was conducted in PubMed, Scopus, and Google Scholar electronic databases to identify original articles and reviews in English or French of traumatic and non-traumatic MO. Studies were selected by 2 independent reviewers following the PRISMA recommendation and descriptive data were extracted. We harvest in each case the sex, age at diagnosis, location, presence of initial trauma, pre-emptive diagnosis, modalities of imagery used, realized biopsy, treatment performed, and type of follow-up. Sixty pediatric cases of MO were identified between 2002 and 2023. Twenty-three patients (38.3%) were diagnosed with idiopathic/pseudomalignant and 37 patients (61.7%) with circumscribed. The mean age at diagnosis was 9.5 years (range 0.2-17 years), with a male-to-female ratio of 1:1. The initial pre-emptive diagnosis was neoplasia in 13 patients (21.7%). The biopsy was percutaneous in 9 patients (15%) and incisional in 7 patients (11.7%). Histological analysis was achieved in 35 cases (57%). Surgical excision was the first line treatment in 46.7% of patients, and non-surgical in the remaining patients. The follow-up strategy was clinical in 16 patients (26.7%) or based on imaging investigation in 23 patients (38.3%). Although MO in children is described as a rare pathology, identifying the benignity of the condition is essential to avoid unnecessary invasive treatment and to avoid delaying the treatment of a potentially life-threatening entity. It seems that there is no consensus established concerning the proper imaging for diagnosis. Clinicians should acknowledge that the absence of a triggering trauma tends to direct the investigation and the management toward a surgical attitude. Conservative management is key, however, surgical excision can be proposed on matured lesions on a case-by-case basis. The absence of recurrence is not excluded. Therefore, a close clinical follow-up is suggested for all cases. The true benefit of a radiological is questioned in a question known to be self-resolving.

Identifiants

pubmed: 38161430
doi: 10.3389/fped.2023.1295212
pmc: PMC10757320
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1295212

Informations de copyright

© 2023 Cherry, Mutschler, Samara, Merckaert, Zambelli and Tschopp.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Ibrahim Cherry (I)

Department of Pediatric Orthopedic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Marion Mutschler (M)

Department of Pediatric Orthopedic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Eleftheria Samara (E)

Department of Pediatric Orthopedic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Sophie Merckaert (S)

Department of Pediatric Orthopedic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Pierre-Yves Zambelli (PY)

Department of Pediatric Orthopedic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Benjamin Tschopp (B)

Department of Pediatric Orthopedic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Classifications MeSH