Yamagishi Azusa, Kaiho Tomomi, Yotsukura Jiro, Ikeda Jun-Ichiro, Baba Takayuki
Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, JPN.
Department of Diagnostic Pathology, Chiba University Graduate School of Medicine, Chiba, JPN.
Cureus. 2025 Jun 24;17(6):e86646. doi: 10.7759/cureus.86646. eCollection 2025 Jun.
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.
阿达木单抗是一种广泛使用的肿瘤坏死因子(TNF)抑制剂,很少与眼部不良事件相关。在此,我们报告一例在阿达木单抗治疗后发生的双侧多发性睑板腺囊肿病例。一名32岁女性因与泛发性脓疱型银屑病相关的葡萄膜炎接受阿达木单抗治疗,同时患有银屑病关节炎。开始使用阿达木单抗后,她最初的全身和眼部症状有所改善;然而,五个月后,出现了对保守治疗耐药的双侧睑板腺囊肿,需要手术干预。进行了切除手术,组织病理学检查显示为肉芽肿性炎症,伴有上皮样细胞、多核巨细胞、浆细胞和淋巴细胞,符合睑板腺囊肿表现。术后观察到持续性睑缘炎和残留的睑板腺囊肿。随后葡萄膜炎、皮肤病变和关节症状复发,提示阿达木单抗继发失效;因此,治疗改为使用赛妥珠单抗。此后,全身和眼部症状均明显改善。由于该病不寻常的大小、双侧性、多发性和临床病程,阿达木单抗诱导的免疫失衡可能促成了睑板腺囊肿的发生。