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J Pak Med Assoc ; 71(7): 1897-1899, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-34410270

RESUMEN

Chondromyxoid fibroma is a rare tumour, representing <1% of all primary bone neoplasm. We report the case of a four-year-old female child with a one-year history of nasal obstruction and facial swelling. A large enhanced lesion with amorphous densities spreading into the right cribriform plate and floor of sphenoid sinus, laterally into the right lamina papyracea, inferolaterally into the medial wall of maxillary sinus, posteriorly into the nasopharynx and superior aspect of oropharynx was observed on CT scan. The mass was excised by Caldwell Luc's endoscopic medial maxillectomy via sublabial approach. CMF was confirmed histopathologically.


Asunto(s)
Neoplasias Óseas , Fibroma , Niño , Preescolar , Endoscopía , Femenino , Fibroma/diagnóstico por imagen , Fibroma/cirugía , Humanos , Tomografía Computarizada por Rayos X
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