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  Vol. 123 No. 1, January 2005 TABLE OF CONTENTS
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  Clinicopathologic Reports, Case Reports, and Small Case Series
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Systemic Non-Hodgkin B-Cell Lymphoma Encountered as a Vanishing Choroidal Mass

Arch Ophthalmol. 2005;123:105-109.

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

Intraocular lymphomas may be subclassified as primary ocular/central nervous system lymphoma and systemic non-Hodgkin lymphoma. Systemic non-Hodgkin lymphomas are usually B-cell lymphomas but may also be of T cell origin. Although ocular/central nervous system lymphomas may commonly be encountered with ocular involvement, it is rare for systemic non-Hodgkin lymphomas to be seen initially as ocular lesions.1-6 We report the case of a systemic large B-cell, non-Hodgkin lymphoma encountered as a choroidal mass with resolution of the ocular lesion after fine-needle aspiration biopsy.

Report of a Case

A 47-year-old woman sought treatment for sudden decreased vision in her left eye. Best-corrected visual acuity was 20/30 OD and hand movements OS. Intraocular pressure was 18 mm Hg in each eye. A left relative afferent pupillary defect was present. Results of an anterior segment examination were unremarkable in both eyes. Dilated ophthalmoscopic examination was unremarkable in the right eye, but disclosed a total, bullous serous retinal detachment . . . [Full Text of this Article]


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AUTHOR INFORMATION
Rajendra S. Apte, MD, PhD; Nael A. Al-Abdulla, MD; W. Richard Green, MD; Andrew P. Schachat, MD; M. Robert DeJong, RDMS, RDCS, RVT; Cathy DiBernardo, RN, RDMS, ROUB; James T. Handa, MD







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