Congenital Orbital Teratoma.
Ocul Oncol Pathol
; 3(1): 11-16, 2017 Jan.
Article
em En
| MEDLINE
| ID: mdl-28275597
We report a case of congenital orbital teratoma. A 3-day-old male, born at 39 weeks' gestation without relevant prenatal history, presented with a large vascularized proptotic mass distorting the left midface. Laboratory studies showed elevated serum alpha-fetoprotein (12,910 ng/ml). Computed tomography showed a multiloculated heterogeneous lesion composed of hypodense and hyperdense calcified areas encompassing the whole orbital cavity with expansion of the bony walls, as well as forward displacement and compression of the eyeball without extension to surrounding structures. Clinical, imaging and laboratory features were consistent with congenital orbital teratoma. Due to pronounced proptosis with exposure keratopathy and corneal perforation, no motility of the globe and no vision in the affected eye in a resource-limited setting, the patient underwent orbital exenteration. Histopathological examination confirmed the diagnosis of mature cystic teratoma. We describe the clinical course, radiographic and histopathological findings of this rare orbital tumor.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Ocul Oncol Pathol
Ano de publicação:
2017
Tipo de documento:
Article
País de afiliação:
República Dominicana
País de publicação:
Suíça