Your browser doesn't support javascript.
loading
Pediatric myositis ossificans mimicking osteosarcoma.
Yamaga, Kensaku; Kobayashi, Eisuke; Kubota, Daisuke; Setsu, Nokitaka; Tanaka, Yuya; Minami, Yusuke; Tanzawa, Yoshikazu; Nakatani, Fumihiko; Kawai, Akira; Chuman, Hirokazu.
Afiliación
  • Yamaga K; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Kobayashi E; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Kubota D; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Setsu N; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Tanaka Y; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Minami Y; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Tanzawa Y; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Nakatani F; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Kawai A; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Chuman H; Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Pediatr Int ; 57(5): 996-9, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26508182
Myositis ossificans (MO) is a rare benign cause of heterotopic bone formation in soft tissue that most commonly affects young adults, typically following trauma. We report the case of an 11-year-old girl who developed MO mimicking osteosarcoma in her right shoulder. Plain radiography and computed tomography showed poorly defined flocculated densities in the soft tissue and a periosteal reaction along the proximal humerus. On magnetic resonance imaging, the mass displayed an ill-defined margin and inhomogeneous signal change. Histologically, the mass had a pseudosarcomatous appearance. Based on these findings, the patient was initially misdiagnosed with osteosarcoma at another hospital. The diagnosis was difficult because the patient was 11 years old and had no trauma history, with atypical radiographic changes and a predilection for the site of origin for osteosarcomas. We finally made the correct diagnosis of MO by carefully reviewing and reflecting on the pathological differences between stages.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Óseas / Osteosarcoma / Errores Diagnósticos / Miositis Osificante Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans Idioma: En Revista: Pediatr Int Asunto de la revista: PEDIATRIA Año: 2015 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Óseas / Osteosarcoma / Errores Diagnósticos / Miositis Osificante Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans Idioma: En Revista: Pediatr Int Asunto de la revista: PEDIATRIA Año: 2015 Tipo del documento: Article País de afiliación: Japón