TY - JOUR
T1 - Prevalence and causes of clinically detectable uveitic serous retinal detachment
AU - Kinast, Robert M.
AU - Solomon, Sharon D.
AU - Cubillan, Leo D.P.
AU - Hovakimyan, Anna
AU - Acharya, Nisha
AU - Cunningham, Emmett T.
N1 - Publisher Copyright:
© The Author(s) 2021.
PY - 2021/11
Y1 - 2021/11
N2 - Purpose: To describe the prevalence and causes of clinically detectable uveitic serous retinal detachment (SRD). Methods: Retrospective chart review of a large clinic-based series. Results: Serous retinal detachment was present in 78 of the 2761 (2.8%) patients. Vogt-Koyanagi-Harada (VKH) disease was the most commonly identified cause (38/78, 48.7%). Less common associated etiologies included toxoplasmic retinochoroiditis (8/78, 10.3%), sarcoidosis (5/78, 6.4%), intraocular lymphoma (4/78, 5.1%), presumed tuberculosis (3/78, 3.8%), and posterior scleritis (2/78, 2.6%). Fifteen patients (19.2%) with uveitic SRD at presentation had no identifiable etiology and were labeled idiopathic or indeterminant. Thirty of the 38 patients with VKH disease (78.9%) had positive neurological and/or integumentary findings, and therefore constituted either complete or incomplete subtypes of the disease. The remaining eight (21.1%) had presumed/ocular VKH disease limited to the eye. Conclusion: While VKH disease by far is the most common cause of clinically detectable uveitic SRD, a number of other non-infectious and infectious inflammatory disorders were also associated with this distinctive clinical finding.
AB - Purpose: To describe the prevalence and causes of clinically detectable uveitic serous retinal detachment (SRD). Methods: Retrospective chart review of a large clinic-based series. Results: Serous retinal detachment was present in 78 of the 2761 (2.8%) patients. Vogt-Koyanagi-Harada (VKH) disease was the most commonly identified cause (38/78, 48.7%). Less common associated etiologies included toxoplasmic retinochoroiditis (8/78, 10.3%), sarcoidosis (5/78, 6.4%), intraocular lymphoma (4/78, 5.1%), presumed tuberculosis (3/78, 3.8%), and posterior scleritis (2/78, 2.6%). Fifteen patients (19.2%) with uveitic SRD at presentation had no identifiable etiology and were labeled idiopathic or indeterminant. Thirty of the 38 patients with VKH disease (78.9%) had positive neurological and/or integumentary findings, and therefore constituted either complete or incomplete subtypes of the disease. The remaining eight (21.1%) had presumed/ocular VKH disease limited to the eye. Conclusion: While VKH disease by far is the most common cause of clinically detectable uveitic SRD, a number of other non-infectious and infectious inflammatory disorders were also associated with this distinctive clinical finding.
KW - Exudative retinal detachment
KW - Vogt-Koyanagi-Harada disease
KW - inflammation
KW - neurosensory retinal detachment
KW - uveitis
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U2 - 10.1177/1120672121991391
DO - 10.1177/1120672121991391
M3 - Article
C2 - 33530714
AN - SCOPUS:85100556770
SN - 1120-6721
VL - 31
SP - 3093
EP - 3098
JO - European journal of ophthalmology
JF - European journal of ophthalmology
IS - 6
ER -