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  Vol. 120 No. 9, September 2002 TABLE OF CONTENTS
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  Clinicopathologic Reports, Case Reports, and Small Case Series
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Atypical Retinoblastoma Presentations: A Challenge for the Treating Ophthalmologist

Arch Ophthalmol. 2002;120:1222-1225.

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

INTRODUCTION

An intraocular procedure in a child with retinoblastoma represents one of the few situations in which an ophthalmologist can produce a disease that may be fatal to the patient. It is always important to consider retinoblastoma, even in children who are atypical in age or appearance for this disease.


Report of Cases

Case 1

A 19-month-old boy with a medical history of malrotation of the intestines who had recently undergone their surgical repair, was referred for evaluation of leukocoria in his right eye. His ocular history was significant for strabismus at 6 months of age that was attributed to prominent epicanthal folds. At approximately 19 months of age, his right eye clearly deviated, and he was referred to a pediatric ophthalmologist who subsequently referred the patient to the ocular oncology unit at the University of California, San Francisco (UCSF).

On examination at UCSF, the patient demonstrated visual fixation that was not central and not steady . . . [Full Text of this Article]

Case 2

Case 3

Comment

Corresponding author: Joan M. O'Brien, MD, Ocular Oncology Division, Department of Ophthalmology, University of California San Francisco, 10 Koret Way, Room K-301, Box 0730, San Francisco, CA 94143-0730 (e-mail: aleja@itsa.ucsf.edu).



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