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  Vol. 116 No. 6, June 1998 TABLE OF CONTENTS
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  Clinicopathologic Report
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 •Choroidal Neovascularization
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Multifocal Choroiditis

Clinicopathologic Correlation

Arch Ophthalmol. 1998;116:801-803.

Many of the white dot syndromes are considered to have a granulomatous pathogenesis. The histopathologic characteristics of this case of multifocal choroiditis seen within 15 months of apparent clinical onset show that the white dot lesions were nongranulomatous perivascular choroidal infiltrates, consisting mainly of B lymphocytes. Early choroidal neovascularization was also seen.


Anthony A. S. Dunlop, MD; Ian A. Cree, PhD; Susan Hague, MB; Philip J. Luthert, MB; Susan Lightman, MD
From the Departments of Clinical Ophthalmology (Dr Dunlop and Ms Lightman) and Pathology (Dr Cree and Mr Luthert), Institute of Ophthalmology, University College, London, England; and the Department of Ophthalmology, Royal Naval Hospital Haslar, Gosport, England (Ms Hague).



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