Bilateral Multiple Chalazia After Adalimumab Therapy for Uveitis Associated With Generalized Pustular Psoriasis: A Case Report

Adalimumab is a widely used tumor necrosis factor (TNF) inhibitor that is rarely associated with ophthalmic adverse events. Herein, we report a case of multiple bilateral chalazia that developed after adalimumab therapy. A 32-year-old woman was treated with adalimumab for uveitis associated with generalized pustular psoriasis, with coexisting psoriatic arthritis. She initially experienced systemic and ocular symptom improvement after starting adalimumab; however, five months later, bilateral chalazia resistant to conservative management developed, requiring surgical intervention. Excisional surgery was performed, and a histopathological examination revealed granulomatous inflammation with epithelioid cells, multinucleated giant cells, plasma cells, and lymphocytes consistent with chalazia. Persistent blepharitis and residual chalazia were observed postoperatively. A subsequent relapse of uveitis, skin lesions, and joint symptoms indicated secondary failure of adalimumab; therefore, treatment was switched to certolizumab pegol. Thereafter, both systemic and ocular symptoms markedly improved. Because of the unusual size, bilaterality, multiplicity, and clinical course of the disease, immune imbalance induced by adalimumab may have contributed to chalazia development.

Authors

Institutions

Publication Details

Journal
Cureus
Published
2025-06-24
DOI
https://doi.org/10.7759/cureus.86646
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Bilateral Multiple Chalazia After Adalimumab Therapy for Uveitis Associated With Generalized Pustular Psoriasis: A Case Report

Takayuki Baba, Jiro Yotsukura, Atsushi Yamagishi, Jun‐ichiro Ikeda et al.
Cureus
Psoriasis: Treatment and Pathogenesis
article

Bilateral Multiple Chalazia After Adalimumab Therapy for Uveitis Associated With Generalized Pustular Psoriasis: A Case Report

Takayuki Baba, Jiro Yotsukura, Atsushi Yamagishi, Jun‐ichiro Ikeda, Tomomi Kaiho
article en

Abstract

Adalimumab is a widely used tumor necrosis factor (TNF) inhibitor that is rarely associated with ophthalmic adverse events. Herein, we report a case of multiple bilateral chalazia that developed after adalimumab therapy. A 32-year-old woman was treated with adalimumab for uveitis associated with generalized pustular psoriasis, with coexisting psoriatic arthritis. She initially experienced systemic and ocular symptom improvement after starting adalimumab; however, five months later, bilateral chalazia resistant to conservative management developed, requiring surgical intervention. Excisional surgery was performed, and a histopathological examination revealed granulomatous inflammation with epithelioid cells, multinucleated giant cells, plasma cells, and lymphocytes consistent with chalazia. Persistent blepharitis and residual chalazia were observed postoperatively. A subsequent relapse of uveitis, skin lesions, and joint symptoms indicated secondary failure of adalimumab; therefore, treatment was switched to certolizumab pegol. Thereafter, both systemic and ocular symptoms markedly improved. Because of the unusual size, bilaterality, multiplicity, and clinical course of the disease, immune imbalance induced by adalimumab may have contributed to chalazia development.

CureusVol. 17(6)
Chiba University (JP)
Good health and well-being
Openalex Percentile: Top 84%
Psoriasis: Treatment and Pathogenesis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.