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Case Reports
. 2004 May;221(5):401-3.
doi: 10.1055/s-2004-812858.

[Primary intraocular lymphoma with unusual clinical presentation and poor outcome]

[Article in German]
Affiliations
Case Reports

[Primary intraocular lymphoma with unusual clinical presentation and poor outcome]

[Article in German]
M Pache et al. Klin Monbl Augenheilkd. 2004 May.

Abstract

Background: Primary intraocular lymphoma is a distinct subset of primary non-Hodgkin's lymphoma of the CNS. In general, the primary non-Hodgkin's lymphoma of the CNS is rare, accounting for 1 % of all non-Hodgkin's lymphomas and less than 1 % of all intraocular tumors.

History and signs: A 70-year-old man was hospitalized in June 2002 because of acute loss of vision on his left eye. A severe vitreous hemorrhage was observed. Ultrasound showed solid subretinal lesions at the posterior fundus. Diagnostic vitreous surgery including a biopsy was performed. An intraocular malignant B-cell lymphoma was determined by immunohistochemistry. General screening revealed no further manifestations of the lymphoma.

Therapy and outcome: The patient initially refused any therapy until a painful secondary neovascular glaucoma with complete loss of visual function developed, thus prompting us to perform an enucleation. The following immunohistochemical examination confirmed the initial diagnosis. A chemotherapy with high-dose methotrexate and leucovorin rescue was initiated.

Conclusions: Primary intraocular lymphoma can present as diffuse uveitis refractory to corticosteroids. Diagnosis can be difficult and is often delayed.

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