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Background: To analyze clinical features, treatment, complications, and visual outcomes of ocular sarcoidosis at a tertiary center in Tokyo.
Methods: Clinical records of 53 patients with ocular sarcoidosis ("definite" or "presumed") presenting between 2013 and 2018 to the Kyorin Eye Center were retrospectively reviewed. Diagnosis was based on the revised criteria of the International Workshop on Ocular Sarcoidosis.
Results: Definite (biopsy-proven) disease was present in 87% of patients and presumed disease in 13%. The mean age at presentation was 58 years (13-81 years) and 68% were women. The mean follow-up was 34 months (6-70 months). Forty-five patients (85%) had panuveitis, and the most common ocular clinical sign suggestive of ocular sarcoidosis was bilaterality (92%). Ocular complications were observed in 93 eyes (85%), most commonly cataract (73%), epiretinal membrane (24%), macular edema (24%) and glaucoma (19%). Thirty-one eyes (30%) underwent cataract surgery and 12 eyes (12%) underwent pars plana vitrectomy. Ten patients (19%) received systemic corticosteroid therapy and 33 eyes (32%) received periocular corticosteroid injections. The best-corrected visual acuity was 1.0 or better in 51% of eyes at presentation, 57% at 6 months, 50% at 12 months, and 58% at 36 months.
Conclusions: The majority of ocular sarcoidosis patients were women, had bilateral disease and panuveitis involvement. Most eyes maintained good visual acuity, although surgical interventions for cataract and epiretinal membrane were common.
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http://dx.doi.org/10.1007/s00417-022-05701-x | DOI Listing |
Eur J Ophthalmol
August 2025
Manchester Royal Eye Hospital, Manchester, UK.
IntroductionConjunctival involvement in sarcoidosis typically presents as non-scarring granulomatous inflammation; however, cicatricial conjunctivitis represents a rare and poorly characterised manifestation. There are currently no published reports of sarcoid-related conjunctival granulomas with cicatrising features responding to anti-TNF therapy. We present the first case of biopsy-confirmed conjunctival sarcoidosis with progressive scarring successfully treated with adalimumab after failure of conventional immunosuppression.
View Article and Find Full Text PDFOpen Med (Wars)
August 2025
Hunan University of Traditional Chinese Medicine, Changsha, Hunan, 410208, China.
Background: Sarcoidosis is characterized by the proliferation of noncaseating granulomas and presents as a complex chronic inflammatory disease. Autophagy plays a crucial role in the initiation, progression, and treatment resistance of various cancers. Despite the recognized importance of autophagy, the involvement of autophagy-related genes (ARGs) in the pathophysiology of ocular sarcoidosis (OS) remains largely unexplored.
View Article and Find Full Text PDFOcul Immunol Inflamm
August 2025
Department of Uveitis & Ocular Inflammation, Vittala International Institute of Ophthalmology, Prabha Eye clinic & Research Centre, Bengaluru, India.
Purpose: We aim to look at the clinical profile in paediatric ocular sarcoidosis in a tertiary eye centre from South India.
Methods: Retrospective study between 2012 and 2024.
Results: A total of 29 cases of paediatric ocular sarcoidosis including 19 cases of late onset sarcoid and 10 cases of early onset sarcoid/Blau syndrome were retrieved from our medical database.
Ocul Immunol Inflamm
July 2025
Miyata Eye Hospital, Miyakonojo, Japan.
Purpose: To investigate the epidemiology, clinical features, laterality, and long-term visual prognosis of uveitis.
Methods: This is a retrospective observational study.
Results: We included 1362 patients diagnosed with uveitis at Miyata Eye Hospital, Japan, from 2015 to 2020.
CNS Neurol Disord Drug Targets
July 2025
School of Medicine, Universidade Federal do Cariri, Juazeiro do Norte, Brazil.
Introduction: Neurosarcoidosis is a rare and severe manifestation of sarcoidosis, whose natural history still lacks a comprehensive and theoretical understanding. Therefore, we aimed to conduct a qualitative systematic review of the literature on the clinical-epidemiologic, diagnostic, and therapeutic assessment of patients with neurosarcoidosis.
Methods: A qualitative systematic literature review was conducted in accordance with the PRISMA protocol.