Ocular sarcoidosis: clinical experience and recent pathogenetic and therapeutic advancements.

Angiotensin-converting enzyme Bronchoalveolar lavage Ocular sarcoidosis T-lymphocyte Uveitis

Journal

International ophthalmology
ISSN: 1573-2630
Titre abrégé: Int Ophthalmol
Pays: Netherlands
ID NLM: 7904294

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 29 01 2020
accepted: 21 07 2020
pubmed: 3 8 2020
medline: 22 6 2021
entrez: 3 8 2020
Statut: ppublish

Résumé

To describe the ocular manifestations in a cohort of patients with systemic sarcoidosis (SS). Recent advances in the pathophysiology, diagnosis, and therapy of SS are also discussed. Data from 115 Italian patients diagnosed between 2005 and 2016 were retrospectively reviewed. All but the first 17 patients underwent a comprehensive ophthalmologic examination. The diagnosis was based on clinical features, the demonstration of non-caseating granulomas in biopsies from involved organs, and multiple imaging techniques. Data on broncho-alveolar lavage fluid analysis, calcemia, calciuria, serum angiotensin-converting enzyme levels and soluble interleukin-2 receptor levels were retrieved when available. Ocular involvement, detected in 33 patients (28.7%), was bilateral in 29 (87.9%) and the presenting feature in 13 (39.4%). Anterior uveitis was diagnosed in 12 patients (36.4%), Löfgren syndrome and uveoparotid fever in one patient each (3%), intermediate uveitis in 3 patients (9.1%), posterior uveitis in 7 (21.2%), and panuveitis in 9 (27.3%). First-line therapy consisted of corticosteroids, administered as eyedrops (10 patients), sub-Tenon's injections (1 patient), intravitreal implants (9 patients), or systemically (23 patients). Second-line therapy consisted of steroid-sparing immunosuppressants, including methotrexate (10 patients) and azathioprine (10 patients). Based on pathogenetic indications that tumor necrosis factor (TNF)-α is a central mediator of granuloma formation, adalimumab, targeting TNF-α, was employed in 6 patients as a third-line agent for severe/refractory chronic sarcoidosis. Uveitis of protean type, onset, duration, and course remains the most frequent ocular manifestation of SS. Diagnostic and therapeutic advancements have remarkably improved the overall visual prognosis. An ophthalmologist should be a constant component in the multidisciplinary approach to the treatment of this often challenging but intriguing disease.

Identifiants

pubmed: 32740881
doi: 10.1007/s10792-020-01531-0
pii: 10.1007/s10792-020-01531-0
pmc: PMC7669777
doi:

Substances chimiques

Adalimumab FYS6T7F842

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3453-3467

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Auteurs

Rosanna Dammacco (R)

Department of Ophthalmology and Neuroscience, University of Bari "Aldo Moro", Medical School, Bari, Italy.

Jyotirmay Biswas (J)

Department of Uveitis and Ocular Pathology, Sankara Nethralaya, Chennai, India.

Tero T Kivelä (TT)

Department of Ophthalmology, University of Helsinki, Helsinki, Finland.

Francesco Alfredo Zito (FA)

Pathology Department, IRCCS-Istituto Tumori 'Giovanni Paolo II', Bari, Italy.

Patrizia Leone (P)

Department of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", Medical School Polyclinic, Piazza Giulio Cesare, 11, 70124, Bari, Italy.

Alberto Mavilio (A)

Social Health District, Glaucoma Center, Azienda Sanitaria Locale, Brindisi, Italy.

Dario Sisto (D)

Department of Ophthalmology and Neuroscience, University of Bari "Aldo Moro", Medical School, Bari, Italy.

Giovanni Alessio (G)

Department of Ophthalmology and Neuroscience, University of Bari "Aldo Moro", Medical School, Bari, Italy.

Franco Dammacco (F)

Department of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", Medical School Polyclinic, Piazza Giulio Cesare, 11, 70124, Bari, Italy. francesco.dammacco@uniba.it.

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