PARACENTRAL ACUTE MIDDLE MACULOPATHY ASSOCIATED WITH BRANCH RETINAL ARTERY OCCLUSION DUE TO POLYCYTHEMIA IN A PATIENT WITH TETRALOGY OF FALLOT.
Retin Cases Brief Rep
; 16(5): 558-560, 2022 Sep 01.
Article
em En
| MEDLINE
| ID: mdl-32969982
ABSTRACT
PURPOSE:
To describe the occurrence of paracentral acute middle maculopathy (PAMM) associated with branch retinal artery occlusion secondary to polycythemia in a patient with tetralogy of Fallot.METHODS:
Case report.RESULTS:
A 30-year-old man presented with acute vision loss and superior visual deficit in his left eye for two days. His medical record had a tetralogy of Fallot. Complete blood count showed an erythrocyte count of 9.88 million/µL (4.4-5.6), hemoglobin of 17.7 g/dL (13.5-16.9), and hematocrit of 65.4% (40-49). The best-corrected visual acuity was 20/25 in the left eye, and a diagnosis of left inferotemporal branch retinal artery occlusion was made. Spectral-domain optical coherence tomography revealed a characteristic hyperreflective band-like lesion on the inner nuclear layer consistent with PAMM. CONLUSION Polycythemia may be a trigger for branch retinal artery occlusion-associated PAMM. We suggest a new precursor cause of PAMM that is previously undescribed.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Policitemia
/
Doenças Retinianas
/
Tetralogia de Fallot
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Oclusão da Artéria Retiniana
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Degeneração Macular
Idioma:
En
Ano de publicação:
2022
Tipo de documento:
Article