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Bilateral central serous retinopathy in a patient with paroxysmal nocturnal hemoglobinuria treated with deferoxamine

Abstract

Purpose

To report a case of acute bilateral central serous retinopathy associated with deferoxamine therapy in the context of paroxysmal nocturnal hemoglobinuria.

Methods

Spectral-domain optical coherence tomography and fundus autofluorescence were used to investigate posterior segment changes.

Results

A 76-year-old man with paroxysmal nocturnal hemoglobinuria and hereditary spherocytosis was started on deferoxamine for iron overload secondary to previous blood transfusions. Four days after initiation of treatment, he developed bilateral reduced vision and metamorphopsia. He was noted to have bilateral central serous retinopathy. Symptoms and serous retinal detachment resolved rapidly following discontinuation of treatment.

Conclusions

This case represents the first report of acute bilateral central serous retinopathy associated with deferoxamine therapy. Cessation of deferoxamine resulted in rapid visual recovery.

Eur J Ophthalmol 2016; 26(6): e152 - e154

Article Type: CASE REPORT

DOI:10.5301/ejo.5000840

Authors

Kaveh Vahdani, Georgios Makrygiannis, Harikesh Kaneshyogan, Inderpaul S. Sian, Osama Giasin

Article History

Disclosures

Financial support: No financial support was received for this submission.
Conflict of interest: None of the authors has conflict of interest with this submission.

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Authors

Affiliations

  •  Royal Eye Infirmary, Derriford Hospital, Plymouth - UK
  •  Bristol Eye Hospital, Bristol - UK
  •  Ophthalmology Department, Torbay Hospital, Torquay, Devon - UK
  •  Ophthalmology Department, Singleton Hospital, Sketty, Swansea - UK

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