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Purtscher-like retinopathy associated with primary hypereosinophilic syndrome
Omesh P Gupta1, Eric Zegere, Joseph I Maguire
1From the *Retina Service, Wills Eye Institute, Jefferson Medical College, Philadelphia, Pennsylvania; and the †Hematology/Oncology Service, Lankenau Hospital, Wynnewood, Pennsylvania.
Purpose:
To describe a patient with undiagnosed primary hypereosinophilic syndrome (HES) who presented with Purtscher-like retinopathy and to review the literature.
Methods:
Observational case report.
Patient:
A 25-year-old man presented with a 1-week history of bilateral visual blur. Examination revealed multiple peripapillary cotton-wool spots and few intraretinal hemorrhages. Clinical history was obtained and fluorescein angiography, systemic evaluation, laboratory studies, and histopathologic analysis of a bone marrow biopsy specimen were performed.
Results:
The patient was diagnosed with primary HES. No previous description was found in the literature.
Conclusion:
HES should be considered in the differential diagnosis of Purtscher retinopathy. This case supports the microembolic theory of Purtscher retinopathy.
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