Kayabaşı Mustafa, Kefeli Işıl, Çakar Özdal Pınar, Saatci Ali Osman
Department of Ophthalmology, Mus State Hospital, Mus, Turkey.
Department of Ophthalmology, Dokuz Eylul University, Izmir, Turkey.
Eur J Case Rep Intern Med. 2024 Mar 11;11(4):004360. doi: 10.12890/2024_004360. eCollection 2024.
A case of ocular bartonellosis under anti-tumour necrosis factor treatment is described.
A 29-year-old woman with psoriasis who had been on certolizumab treatment was examined with a left visual deterioration following a fever bout, malaise, and placoid erythematous rashes on her neck. As there was acute anterior uveitis in her left eye, it was recommended to stop certolizumab treatment for a possible infectious aetiology. However, her physician elected to continue the certolizumab treatment. Ten days later, the patient noticed further visual decline despite the topical steroid treatment. This time, there were scattered yellow-white small retinitis foci at the left posterior pole. Infectious agents were searched and while antibodies were negative for immunoglobulin M, the immunoglobulin G titre was 1/80. Clinical findings were improved with the systemic treatment of oral trimethoprim-sulfamethoxazole (160/800 mg twice daily for six weeks) and azithromycin (500 mg once daily for two weeks).
Though extremely rare, ocular bartonellosis should be kept in mind in patients on anti-tumour necrosis factor treatment as rapid and accurate diagnosis may end up with an excellent visual outcome and full recovery.
Anti-tumour necrosis factor treatment is fraught with several ocular side effects including myositis, corneal infiltrates, scleritis, uveitis, optic neuritis, retinal vasculitis and ophthalmoplegia.When a new uveitis episode occurs in cases undergoing anti-tumour necrosis factor therapy, its cause poses a diagnostic challenge as it can have either an infectious or a non-infectious nature.Though very rare, ocular bartonellosis may also occur in immunocompromised individuals and a prompt diagnosis and appropriate treatment can lead to an excellent visual recovery.
本文描述了一例在接受抗肿瘤坏死因子治疗期间发生的眼部巴尔通体病病例。
一名29岁患有银屑病的女性,正在接受赛妥珠单抗治疗,在一次发热、全身不适以及颈部出现扁平状红斑疹后,出现左眼视力下降。由于其左眼存在急性前葡萄膜炎,鉴于可能的感染病因,建议停用赛妥珠单抗治疗。然而,她的医生选择继续使用赛妥珠单抗治疗。十天后,尽管进行了局部类固醇治疗,患者仍注意到视力进一步下降。此时,在左眼后极部出现了散在的黄白色小视网膜病灶。对感染病原体进行了检查,免疫球蛋白M抗体为阴性,而免疫球蛋白G滴度为1/80。通过口服甲氧苄啶 - 磺胺甲恶唑(160/800毫克,每日两次,共六周)和阿奇霉素(500毫克,每日一次,共两周)的全身治疗,临床症状得到改善。
尽管极为罕见,但对于接受抗肿瘤坏死因子治疗的患者,应考虑到眼部巴尔通体病,因为快速准确的诊断可能会带来极佳的视力预后和完全康复。
抗肿瘤坏死因子治疗存在多种眼部副作用,包括肌炎、角膜浸润、巩膜炎、葡萄膜炎、视神经炎、视网膜血管炎和眼肌麻痹。在接受抗肿瘤坏死因子治疗的患者中出现新的葡萄膜炎发作时,其病因构成诊断挑战,因为它可能具有感染性或非感染性。尽管非常罕见,但眼部巴尔通体病也可能发生在免疫功能低下的个体中,及时诊断和适当治疗可导致极佳的视力恢复。