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Original Article

Intravascular Lymphoma Mimicking a Vogt-Koyanagi-Harada Disease

, MD, PhD, , MD, PhD, , MD, PhD, , MD, , MD, PhD & , MD, PhD
Pages 132-134 | Received 02 Jul 2010, Accepted 11 Oct 2010, Published online: 23 Mar 2011
 

Abstract

Purpose: To report a case of intravascular lymphoma (IVL) mimicking a Vogt-Koyanagi-Harada disease (VKH).

Design: Case report.

Methods: A 38-year-old man was referred for blurred vision, headache, and hearing loss. Examination demonstrated vitritis and subretinal detachments in each eye. Cerebral fluid analysis showed lymphocytic meningitis. Cerebral MRI was normal. A diagnosis of VKH disease was made.

Results: Steroid treatment was introduced, after which all symptoms disappeared. Six months later, the patient returned with paraplegia and confusion. Cerebral MRI revealed hypodense periventricular lesions. A stereotaxic biopsy confirmed the diagnosis of IVL. The patient died a few months later.

Conclusion: IVL may have many revealing aspects, including ophthalmologic symptoms.

ACKNOWLEDGMENTS

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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