Non-Infectious Choroiditis Subdivided into Its Diverse Pathophysiological Sub-Groups Is the Best-Known and Most Appropriate Nomenclature to Date for the Reclassification and Diagnosis of Former White Dot Entities

dc.contributor.authorДорохова, Олександра Едуардівна
dc.contributor.authorЗборовська, Олександра Володимирівна
dc.date.accessioned2026-07-13T09:35:50Z
dc.date.issued2026
dc.description.abstractWhite dot syndromes (WDS), a purely descriptive term formulated in 1995, grouped inflammatory conditions primarily affecting the choroid that shared the clinical appearance of white dots on fundus examination, thus presenting similar white dots on fundus examination, which, however, had diverse pathophysiologies and different primary localizations of inflammation that did not warrant their association. Some of them, including birdshot retinochoroiditis (BRC) and sympathetic ophthalmia, produced predominant inflammation in the choroidal stroma, while others, including multiple evanescent white dot syndrome (MEWDS) and acute posterior multifocal placoid pigment epitheliopathy (APMPPE), caused inflammatory non-perfusion of the choriocapillaris. The aim of this review is to build upon a pathophysiology-based classification framework that groups these entities under the broader concept of non-infectious choroiditis and subdivides them according to their predominant inflammatory mechanisms and anatomical localization. This framework distinguishes diseases characterized by inflammatory occlusion of the choriocapillaris with consequent perfusion dysfunction, including MEWDS, APMPPE, multifocal choroiditis (MFC), and serpiginous choroiditis, from conditions primarily involving inflammatory infiltration of the choroidal stroma, such as birdshot retinochoroiditis (BRC), Vogt-Koyanagi-Harada disease (VKH), and sympathetic ophthalmia. Moreover, the review raises the question of how such an inadequate term, based on unscientific assumptions, could gain such quick access to ophthalmic practice and literature, be immediately adopted in major textbooks, and persist for so long being unrecognized as a misnomer. The slow and progressive reevaluation of this nomenclature over more than two decades is related and contextualized.
dc.identifier.citationHerbort Jr CP, Silpa-archa S, Papasavvas I, Bouchenaki N, Byszewska A, Dorokhova O, Fardeau C, Hedayatfar A, Hwang D-K, Lages V, et al. Non-Infectious Choroiditis Subdivided into Its Diverse Pathophysiological Sub-Groups Is the Best-Known and Most Appropriate Nomenclature to Date for the Reclassification and Diagnosis of Former White Dot Entities. Diagnostics. 2026; 16(11):1735. https://doi.org/10.3390/diagnostics16111735
dc.identifier.doihttps://doi.org/10.3390/diagnostics16111735
dc.identifier.urihttps://reposit.institut-filatova.com.ua/handle/123456789/1986
dc.language.isoen
dc.subjectnon-infectious choroiditis
dc.subjectchoriocapillaritis
dc.subjectPrimary Inflammatory Choriocapillaropathies (PICCPs)
dc.subjectstromal choroiditis
dc.subjectPrimary Inflammatory Stromal Choroiditis (PISC)
dc.subjectMultiple Evanescent White Dot Syndrome (MEWDS)
dc.subjectAcute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE)
dc.subjectMultifocal Choroiditis (MFC)
dc.subjectserpiginous choroiditis
dc.subjectVOGT-Koyanagi-Harada disease (VKH)
dc.subjectBirdshot Retinochoroiditis (BRC)
dc.subjectIndocyanine Green Angiography (ICGA)
dc.titleNon-Infectious Choroiditis Subdivided into Its Diverse Pathophysiological Sub-Groups Is the Best-Known and Most Appropriate Nomenclature to Date for the Reclassification and Diagnosis of Former White Dot Entities
dc.typeArticle

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