Inokuchi Chie, Sato Shigeru, Terada Makoto, Uematsu Sato, Shirai Setsuko
Ophthalmology, Itami City Hospital, Itami, JPN.
Ophthalmology, Osaka University, Osaka, JPN.
Cureus. 2024 Aug 16;16(8):e66984. doi: 10.7759/cureus.66984. eCollection 2024 Aug.
Cogan syndrome (CS) is a rare chronic inflammatory disease characterized by ocular and inner ear inflammation. Well-known ocular manifestations include non-syphilitic interstitial keratitis (IK); however, some cases are not associated with IK. Inner ear symptoms include sensorineural hearing loss, rotatory vertigo, and tinnitus, which can become irreversible without timely treatment. Therefore, early and appropriate diagnosis and therapeutic intervention are important. However, due to its rarity, few physicians have encountered CS and early diagnosis is difficult. In this report, we present the details of the diagnosis and treatment of an atypical CS. The patient was a 44-year-old Japanese woman who was admitted to the Department of Immunology and Allergy at Itami City Hospital (Itami City, Hyogo, Japan) due to a persistent fever of approximately 40°C for nine days. Multiple erythematous lesions appeared on both lower legs, and she experienced decreased vision in her left eye. Uveitis with retinal vasculitis was observed in both eyes and the optic nerve head showed remarkable swelling in the left eye. Hearing tests revealed impaired hearing in both ears. Based on these findings, we diagnosed atypical CS and initiated systemic and topical steroid therapy. Approximately two weeks later, visual acuity and hearing levels improved. Fluorescein angiography (FA) revealed a non-perfusion area in both eyes, and retinal photocoagulation was performed using a pattern-scanning laser. Eighteen months after the laser irradiation, retinal neovascularization (RNV) was observed in the area where the laser was applied to the left eye; therefore, an additional laser was applied. Combination therapy with steroids and immunosuppressive drugs was continued until the patient's last visit three years later and she did not experience any recurrence of uveitis or hearing loss. In this case, a pattern-scanning laser was used for retinal photocoagulation to prevent RNV; however, RNV occurred within the area of the laser spots. In such cases of retinal capillary occlusion due to vasculitis, it may be better to close the spacing or use a conventional laser system. In the presence of retinal vasculitis with systemic inflammation, CS should be suspected, and a hearing test should be performed, even in the absence of subjective symptoms. Early treatment and prevention of irreversible hearing loss should be necessary. Careful follow-up in collaboration with other departments is important for CS cases.
科根综合征(CS)是一种罕见的慢性炎症性疾病,其特征为眼部和内耳炎症。常见的眼部表现包括非梅毒性间质性角膜炎(IK);然而,部分病例与IK无关。内耳症状包括感音神经性听力损失、旋转性眩晕和耳鸣,若不及时治疗,这些症状可能会变得不可逆。因此,早期且恰当的诊断和治疗干预很重要。然而,由于其罕见性,很少有医生遇到过CS,早期诊断困难。在本报告中,我们呈现了一例非典型CS的诊断和治疗细节。患者为一名44岁的日本女性,因持续发热约40°C九天而入住伊丹市立医院(日本兵库县伊丹市)免疫与过敏科。双下肢出现多个红斑性病变,且她左眼视力下降。双眼均观察到葡萄膜炎伴视网膜血管炎,左眼视神经乳头显著肿胀。听力测试显示双耳听力受损。基于这些发现,我们诊断为非典型CS,并开始全身及局部类固醇治疗。大约两周后,视力和听力水平有所改善。荧光素血管造影(FA)显示双眼有非灌注区,使用模式扫描激光进行了视网膜光凝。激光照射18个月后,在左眼接受激光治疗的区域观察到视网膜新生血管(RNV);因此,又进行了一次激光治疗。继续使用类固醇和免疫抑制药物进行联合治疗,直到三年后患者最后一次就诊,她未出现葡萄膜炎或听力损失的复发。在本病例中,使用模式扫描激光进行视网膜光凝以预防RNV;然而,RNV出现在激光光斑区域内。在因血管炎导致视网膜毛细血管阻塞的此类病例中,缩小光斑间距或使用传统激光系统可能更好。在存在伴有全身炎症的视网膜血管炎时,即使没有主观症状,也应怀疑CS,并进行听力测试。早期治疗和预防不可逆的听力损失很有必要。对于CS病例,与其他科室协作进行仔细的随访很重要。