Atypical case of choroidal osteoma associated to polypoidal choroidal vasculopathy and preretinal neovascular membrane.

Choroidal osteoma ICG-angiography OCT-angiography aneurysmal type 1 neovascularization multimodal imaging neovascular membrane polypoidal choroidal vasculopathy

Journal

European journal of ophthalmology
ISSN: 1724-6016
Titre abrégé: Eur J Ophthalmol
Pays: United States
ID NLM: 9110772

Informations de publication

Date de publication:
22 Apr 2024
Historique:
medline: 22 4 2024
pubmed: 22 4 2024
entrez: 22 4 2024
Statut: aheadofprint

Résumé

To report a very rare and atypical case of an elderly Caucasian female patient who developed perilesional multiple polypoidal choroidal vasculopathy (PCV) as a probable complication of choroidal osteoma (CO), associated to preretinal neovascular membrane overlying the lesion. Observational case report. A 60-year-old Caucasian woman presented with blurred vision in her right eye (RE). Fundus examination revealed a round white-yellowish calcified deep lesion in the juxta-papillary superior area, measuring 4 disc-diameters, with well-defined scalloped margins and an irregular surface. B-scan ultrasonography and orbital tomography confirmed the diagnosis of choroidal osteoma (CO). Further investigation with multimodal imaging including infracyanine green angiography, fluorescein angiography, swept source optical coherence tomography and angiography highlighted the presence of multiple aneurysmal choroidal dilations around the CO, corresponding to PCV. We also noted the presence of a preretinal neovascular membrane overlying the CO. The patient was monitored with regular follow-up since no signs of activity were detected on multimodal imaging. Our case report represents an exceptional and atypical association between pre-retinal neovascularization, PCV and choroidal osteoma. While the mechanisms underlying the development of PCV and pre-retinal neovascularization in the setting of CO are not well understood, it is imperative for ophthalmologists to recognize this association as a potential cause of sudden vision loss in patients with CO, and to consider appropriate diagnostic and management strategies.

Identifiants

pubmed: 38644785
doi: 10.1177/11206721241249218
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11206721241249218

Déclaration de conflit d'intérêts

Declaration of conflicting interestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Mohamed Ben Brahem (M)

Department of ophthalmology A, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.
Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.

Khaled El Matri (K)

Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.
Department of ophthalmology B, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.
Oculogenetic laboratory LR14SP01, Tunis, Tunisia.

Yousra Fafloul (Y)

Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.
Department of ophthalmology B, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.
Oculogenetic laboratory LR14SP01, Tunis, Tunisia.

Amel Chebbi (A)

Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.
Department of ophthalmology C, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.

Olfa Fekih (O)

Department of ophthalmology A, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.
Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.

Leila Nacef (L)

Department of ophthalmology A, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.
Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.

Leila El Matri (L)

Faculté de médecine de Tunis, Université Tunis - El Manar, Tunis, Tunisia.
Department of ophthalmology B, Institut Hédi Raies d'ophtalmologie de Tunis, Tunis, Tunisia.
Oculogenetic laboratory LR14SP01, Tunis, Tunisia.

Classifications MeSH