[Acute posterior multifocal placoid pigment epitheliopathy, serpiginous choroiditis and related diseases].
Épithéliopathie en plaque, choroïdite serpigineuse et leurs formes frontières.
APMPPE
Acute posterior multifocal placoid pigment epitheliopathy
Ampiginous choroiditis
Choroïdite ampigineuse
Choroïdite serpigineuse
Maculopathie placoïde persistante
Persistant placoid maculopathy
Relentless placoid chorioretinitis
Serpiginous choroïdopathy
Syndrome des taches blanches
Épithéliopathie en plaque
Journal
Journal francais d'ophtalmologie
ISSN: 1773-0597
Titre abrégé: J Fr Ophtalmol
Pays: France
ID NLM: 7804128
Informations de publication
Date de publication:
Jun 2023
Jun 2023
Historique:
received:
06
03
2023
revised:
24
03
2023
accepted:
24
03
2023
medline:
19
6
2023
pubmed:
27
5
2023
entrez:
26
5
2023
Statut:
ppublish
Résumé
Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) and serpiginous choroiditis are two diseases classified as "white spot syndromes." Both are inflammatory/autoimmune diseases with suspected primary involvement of the choriocapillaris. The former usually has an excellent prognosis, while the latter can rapidly induce legal blindness. Whereas these diseases are well defined and well known, other entities (such as persistent placoid maculopathy or ampiginous choroiditis) with features of both APMPPE and serpiginous choroiditis have been described more recently. This review aims to describe demographic characteristics and multimodal imaging features to help differentiate between these four diseases.
Identifiants
pubmed: 37236884
pii: S0181-5512(23)00223-1
doi: 10.1016/j.jfo.2023.03.003
pii:
doi:
Types de publication
English Abstract
Journal Article
Review
Langues
fre
Sous-ensembles de citation
IM
Pagination
646-657Informations de copyright
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