Absence of the foveal avascular zone in a nanophthalmic child revealed by optical coherence tomography angiography.
Absence of foveal avascular zone
Nanophthalmos
OCT angiography
Journal
American journal of ophthalmology case reports
ISSN: 2451-9936
Titre abrégé: Am J Ophthalmol Case Rep
Pays: United States
ID NLM: 101679941
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
received:
05
04
2018
revised:
25
08
2018
accepted:
12
09
2018
entrez:
5
12
2018
pubmed:
5
12
2018
medline:
5
12
2018
Statut:
epublish
Résumé
Optical coherence tomography angiography (OCTA) is a new non-invasive imaging technique that does not require the use of contrast agents and that allows the visualization of the retinal microvasculature in a layer-by-layer manner without bright light. This merit allows us to obtain the fundus image in children. Retinal vessels are typically absent from the center of the fovea, an area known as the foveal avascular zone (FAZ). The purpose of the present case study was to evaluate the FAZ in a nanophthalmic pediatric patient with OCTA. A 6-year-old girl was referred to the Hiroshima University Hospital because of her poor vision. She had a best-corrected visual acuity of 20/125 in the right eye and of 20/100 in the left eye. The refractive errors after the administration of atropine sulfate eye drops were +13.00D in the right eye and +14.00D in the left eye. The axial lengths were 17.03 mm in the right eye and 16.90 mm in the left eye. At 9 years of age, the patient was diagnosed with nanophthalmos and OCTA was used to investigate the superficial and deep retinal layers. We demonstrated that the FAZ could not be observed in either eye, whereas the FAZ was readily observed in both eyes of a control subject of similar age. OCTA is a useful technique to reveal the absence of the FAZ in cases of nanophthalmos. Because OCTA is a non-invasive and rapid procedure that is ideal for use with children.
Identifiants
pubmed: 30511032
doi: 10.1016/j.ajoc.2018.09.007
pii: S2451-9936(18)30091-4
pmc: PMC6257928
doi:
Types de publication
Case Reports
Langues
eng
Pagination
34-37Références
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