Orbital Sarcoidosis: A Brief Guide to an Insidious Disease
Donika I Vezirska, Vladimir S Prandzhev

TL;DR
Orbital sarcoidosis is a rare and hard-to-diagnose disease that mimics other conditions, often leading to delayed treatment.
Contribution
A systematic review of the literature on orbital sarcoidosis, focusing on its clinical presentation, diagnosis, and management.
Findings
Orbital sarcoidosis often mimics other pathologies, leading to delayed diagnosis.
The review highlights the challenges in diagnosing and managing this rare condition.
Current data is based on 18 articles, including case reports and original studies.
Abstract
Sarcoidosis is a rare systemic disease that can affect any organ. Orbital manifestations constitute an uncommon extrapulmonary form of sarcoidosis. The symptoms and imaging findings can mimic those of other pathologies, such as orbital pseudotumor lesions, thus delaying clinical diagnosis and adequate treatment. We systematically reviewed the existing literature on the topic, published in PubMed and Google Scholar, up to August 2025, regarding the etiology, clinical presentation of the disease, diagnostic methods, and management. Search words included “orbital sarcoidosis,” “sarcoidosis/”orbital,” and variations of these terms. Only English-language articles were selected. All broader articles that dealt with ocular sarcoidosis or neurosarcoidosis were excluded. The literature review is based on 18 articles (case reports, case studies, and original articles). It presents the current…
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Taxonomy
TopicsSarcoidosis and Beryllium Toxicity Research · IgG4-Related and Inflammatory Diseases · Ocular Diseases and Behçet’s Syndrome
