Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
2.
Jt Dis Relat Surg ; 32(2): 514-520, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34145831

RESUMO

Osteochondromas are neoplasm that belong to the family of cartilaginous histogenesis tumors and represent 90% of all forms of exostoses. As most osteochondromas are asymptomatic, underdiagnosis is frequent. Symptomatic forms usually manifest before the age of 20 years, and the most common symptoms are pain and the detection of a bony mass. Herein, we report four cases of spontaneous regression of solitary osteochondromas in the light of literature. We consider that orthopedic surgeons should take into account the possibility of spontaneous regression of these tumors, before recommending surgery. Symptoms are usually mild and we recommend following these patients with X-ray and physical examination annually.


Assuntos
Neoplasias Ósseas/fisiopatologia , Exostose/fisiopatologia , Regressão Neoplásica Espontânea/fisiopatologia , Osteocondroma/fisiopatologia , Neoplasias Ósseas/diagnóstico por imagem , Criança , Pré-Escolar , Exostose/diagnóstico por imagem , Humanos , Masculino , Osteocondroma/diagnóstico por imagem , Espanha
3.
J Pediatr Surg ; 46(7): E5-8, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21763824

RESUMO

Myositis ossificans circumscripta (MOC), with nonneoplastic heterotopic bone formation in soft tissue and skeletal muscle, is rare in children. Extraskeletal osteosarcoma is a very rare malignant mesenchymal neoplasm of soft tissues in children. At onset, it may be difficult to distinguish MOC from a musculoskeletal infection or neoplasm, particularly in the absence of trauma, and a biopsy is frequently required. However, differentiating MOC from malignant neoplasm is imperative. We describe the case of a 22-month-old girl who presented with a benign fibrous-myofibroblastic tumor mimicking MOC. However, extraskeletal osteosarcoma was also considered in the differential diagnosis due to the absence of attachment of the lesion to the skeleton. Pathologic findings after a previous needle biopsy and posterior marginal resection exclude both differential diagnoses. Close follow-up during 3 years postoperatively showed no signs of recurrence.


Assuntos
Calcinose/etiologia , Miosite Ossificante/diagnóstico , Neoplasias de Tecido Fibroso/diagnóstico , Neoplasias de Tecidos Moles/diagnóstico , Diagnóstico Diferencial , Feminino , Humanos , Lactente , Imageamento por Ressonância Magnética , Miofibroblastos/patologia , Neoplasias de Tecido Fibroso/diagnóstico por imagem , Neoplasias de Tecido Fibroso/patologia , Neoplasias de Tecido Fibroso/cirurgia , Osteossarcoma/diagnóstico , Radiografia , Neoplasias de Tecidos Moles/diagnóstico por imagem , Neoplasias de Tecidos Moles/patologia , Neoplasias de Tecidos Moles/cirurgia , Coxa da Perna
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA