Congenital proptosis secondary to orbital teratoma. Clinicopathological study.
نویسندگان
چکیده
CASE REPORT A newborn male with right proptosis secondary to a retroocular mass. Ophthalmological examination also showed corneal ulcer and perforation, iris hernia, total ophthalmoplegia, chemosis and eyelid retraction. The histopathology diagnosis was mature teratoma. DISCUSSION Teratomas are tumors composed of a mixture of mature tissues consisting of 3 germ layers. Congenital teratomas of the orbit are very rare and should be included as a possibility in cases with a primary tumor in the orbit.
منابع مشابه
Congenital orbital teratoma
BACKGROUND The occurrence of proptosis at birth is unusual and may be associated with a variety of tumours and structural abnormalities. Congenital orbital teratoma is a rare cause of congenital proptosis. METHODS A case report is presented of a female infant with gross right proptosis. RESULTS Computed tomography demonstrated a characteristic multicystic structure with no intracranial invo...
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A newborn baby had an orbital-intracranial benign teratoma radically excised with preservation of the eye. Three years later she developed recurrent proptosis, and reoperation showed an invasive orbital tumour that histologically was a malignant germ-cell neoplasm. The relationship of the two tumours is discussed. Malignant change in a benign orbital-intracranial teratoma of the newborn has not...
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Teratoma is a rare tumor, containing structures originating from all three germinal layers. The most frequent location of teratoma is the gonads. Orbital teratoma is extremely rare. In 1969, Jensen reported that only 40 cases of orbital teratoma existed in the world. We describe a rare case of orbital teratoma in a 15-day girl who presented with marked proptosis of the left eye. The eyeball was...
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We report on a case of an congenital orbital tumor of impressive size, occurring in a newborn. The patient underwent orbital exenteration with a histopathologic diagnosis of cystic teratoma. The clinicopathological aspects of such a rare disease are commented.
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عنوان ژورنال:
- Archivos de la Sociedad Espanola de Oftalmologia
دوره 88 4 شماره
صفحات -
تاریخ انتشار 2013