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  Vol. 120 No. 7, July 2002 TABLE OF CONTENTS
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  Clinicopathologic Reports, Case Reports, and Small Case Series
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Presumed Iris Hemangioma Associated With Multiple Central Nervous System Cavernous Hemangiomas

Arch Ophthalmol. 2002;120:984-985.

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

We present the unique case of a patient with a vascular iris lesion consistent with a cavernous hemangioma and central nervous system (CNS) cavernous hemangiomas demonstrated by magnetic resonance imaging (MRI). Clinical reports of iris vascular tumors are rare and cases with histopathologic abnormalities are even more uncommon.1 Hemangiomas of the eye are most often associated with posterior segment structures. We could find no previously described association between vascular tumors of the iris and CNS in adults. Most of the modern reports of iris vascular tumors occur in isolation.2-3 There is one case of diffuse congenital hemangiomatosis with a unilateral iris cavernous hemangioma; however, this syndrome appears to be uniformly fatal by age 1 year.4

Report of a Case

A 48-year-old white woman was referred for evaluation after her local ophthalmologist noted an unusual iris mass in her right eye. The patient's medical history was significant for schizophrenia for which she had been treated . . . [Full Text of this Article]


Comment
Corresponding author: Thomas A. Oetting, MD, MS, UIHC, Deptartment of Ophthalmology and Visual Sciences, 200 Hawkins Dr, Iowa City, IA 52242-1091 (e-mail: thomas-oetting@uiowa.edu).



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Arteriovenous malformation of the iris in 14 cases.
Shields et al.
Arch Ophthalmol 2006;124:370-375.
ABSTRACT | FULL TEXT  





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