Orthonotes
Orthonotes
by the.bonestories
v3.0 Fusion
v3.0 Fusion
PubMed Case Report / Series Evidence Low

[Progressive myositis ossificans: Case report].

Revista medica del Instituto Mexicano del Seguro Social | 2022 | Cruz-Escutia NK, Mendoza-Álvarez SA, Hernández-Montez ZI, Palafox-Vargas ML

In-App Reader

Open Source

Journal and index pages often block iframe embedding. This reader keeps the evidence details in Orthonotes and leaves the source page one click away.

Source
PubMed
Type
Case Report / Series
Evidence
Low

Abstract

[Indexed for MEDLINE] Conflict of interest statement: los autores han completado y enviado la forma traducida al español de la declaración de conflictos potenciales de interés del Comité Internacional de Editores de Revistas Médicas, y no fue reportado alguno relacionado con este artículo. 15. World Neurosurg. 2019 Oct;130:95-97. doi: 10.1016/j.wneu.2019.06.165. Epub 2019 Jun 28. Pseudomalignant Myositis Ossificans of the Neck in a Child: Case Report and Review of the Literature. Dubuisson A(1), Lombard A(2), Otto B(3). Author information: (1)Department of Neurosurgery, Centre Hospitalier Universitaire de Liège, Liège, Belgium. Electronic address: A.Dubuisson@chu.ulg.ac.be. (2)Department of Neurosurgery, Centre Hospitalier Universitaire de Liège, Liège, Belgium. (3)Department of Diagnostic and Interventional Neuroradiology, Centre Hospitalier Universitaire de Liège, Liège, Belgium. BACKGROUND: Myositis ossificans is a benign process of heterotopic bone formation developing in soft tissues that can mimic malignancy. Differential diagnosis can be difficult without a biopsy when it originates in atypical locations. CASE DESCRIPTION: A 5½-year-old boy was admitted for a cervical tumor causing torticollis. The nodular tumor developed at the lateral border of the right C3-4 foramen, had calcification/ossification at its periphery, and was accompanied by a huge edematous reaction of the scalene muscles. The patient underwent an extensive work-up by pediatric oncologists. A biopsy was requested because of high suspicion of malignancy. At surgery, the lesion was benign on frozen sections and was completely resected, allowing the diagnosis of myositis ossificans. The patient made a rapid and complete recovery. CONCLUSIONS: Myositis ossificans circumscripta is rare in children, especially in the neck region. The diagnostic challenge is to differentiate it from bone and soft tissue malignancies. Appropriate management, including surgery if needed, leads to an excellent outcome. Another concern is to exclude fibrodysplasia ossificans progressiva when atraumatic myositis ossificans develops in a young child in the neck or shoulder region. Copyright © 2019. Published by Elsevier Inc. DOI: 10.1016/j.wneu.2019.06.165

Linked Wiki Topics

This article has not been linked to a wiki topic yet.

Linked Cases

This article has not been linked to a case yet.

Linked Atlases

This article has not been linked to an atlas yet.