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PARACENTRAL ACUTE MIDDLE MACULOPATHY IN PRIMARY CONGENITAL GLAUCOMA
Yavuz K Aribas1, Zeynep Aktas, Kemal Bayrakceken
1Department of Ophthalmology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Retinal Cases & Brief Reports
|November 21, 2017
Summary
Primary congenital glaucoma may predispose individuals to paracentral acute middle maculopathy. This case report details a 14-year-old girl experiencing sudden vision loss due to this rare association.
Area of Science:
- Ophthalmology
- Medical Case Reports
Background:
- Primary congenital glaucoma (PCG) is a rare developmental disorder affecting infants.
- Paracentral acute middle maculopathy (PAMC) is an ischemic condition affecting the macula.
Observation:
- A 14-year-old female presented with sudden vision loss.
- Ophthalmic examination revealed signs of PCG including Haab striae and optic disc hemorrhages.
- Fundoscopy showed a fern-like white macula lesion.
Findings:
- Optical coherence tomography (OCT) demonstrated hyperreflective plaques in the inner nuclear/outer plexiform layers.
- OCT angiography revealed ischemia in the deep capillary plexuses.
- These OCT findings were consistent with PAMC.
Implications:
- This is the first reported case linking PCG and PAMC.
- PCG may be a predisposing factor for developing PAMC.
- Further research is warranted to understand this association.
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