Solitary infantile myofibromatosis of the orbit
Pan Arab Journal of Neurosurgery. 2003; 7 (2): 70-73
em Inglês
| IMEMR
| ID: emr-64261
ABSTRACT
Infantile myofibromatosis [IM] is an extremely rare cause of skull lesion in the new-born and paediatric population. The prognosis is related to the number of lesions and the presence or absence of visceral involvement. The authors report a case of IM, in a 5-year-old boy with an osteolytic lesion in the right orbital roof, which displaced the globe downwards. A subfrontal approach was made with total resection. The globe had regained a normal position and further evaluation revealed no other lesions. The patient's age at presentation, physical findings, radiographic appearance and the histopathological examination of the lesion are needed to generate a-differential diagnosis and to formulate a treatment plan
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Pediatria
/
Neoplasias Orbitárias
/
Tomografia Computadorizada por Raios X
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Pan Arab J. Neurosurgery
Ano de publicação:
2003
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