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  Vol. 123 No. 8, August 2005 TABLE OF CONTENTS
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  Clinicopathologic Reports, Case Reports, and Small Case Series
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Diffuse Retinal Involvement in Malignant Nonteratoid Medulloepithelioma of Ciliary Body in an Adult

Arch Ophthalmol. 2005;123:1136-1138.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Intraocular medulloepithelioma is a rare embryonal neoplasm that occurs predominantly in children and arises from the primitive medullary epithelium of the optic cup. Medulloepitheliomas that contain heterotopic elements or tissues such as brain, cartilage, or rhabdomyoblasts are classified as teratoid, and tumors lacking these elements are classified as nonteratoid medulloepitheliomas.1 Both nonteratoid and teratoid medulloepitheliomas may be benign or malignant.1

The clinical and histopathological features of intraocular medulloepitheliomas have been described previously in various reports.2-9 We herein report a case of a malignant nonteratoid medulloepithelioma of a ciliary body in an adult. To the best of our knowledge, this is the first documented report of a medulloepithelioma of the ciliary body with intraretinal involvement.

Report of a Case

A 27-year-old Hispanic man developed a mass in the left side of the neck in 1976. A histopathological diagnosis of Hodgkin disease was made. The patient was treated with radiation and chemotherapy. Following treatment, he remained . . . [Full Text of this Article]


Pathologic Findings

Comment

AUTHOR INFORMATION
Ramon L. Font, MD; Kirtee Rishi, MD



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Possible Shared Pathogenesis of the Retinoinvasive Phenotype of Malignant Medulloepithelioma and Malignant Melanoma of the Ciliary Body
Kivela and Summanen
Arch Ophthalmol 2006;124:1066-1066.
FULL TEXT  





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