白内障术后并发假丝酵母样角膜炎致角膜穿孔1例

Brian Hwang, J. Jia, Frank S Hwang
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引用次数: 0

摘要

本研究的目的是报告和记录一例罕见的假丝酵母旁裂性角膜炎,发生在常规角膜透明切口白内障手术后,最终导致穿孔性角膜溃疡,随后需要进行穿透性角膜移植术(PK)。通过这一病例,本研究旨在对现有文献做出贡献,并提高人们对白内障手术并发症的潜在风险的认识。在这个病例报告中,我们描述了一个罕见的真菌感染的表现和处理后,常规白内障摘除在一个80岁的男性患者。患者最初因疑似眼内炎和细菌性角膜炎接受治疗,但症状恶化,包括角膜小穿孔。转诊至诊所后,患者在白内障创面附近出现绒毛状间质浸润、上皮缺损和垂体后叶。开始使用1%局部复配伏立康唑治疗,但未能阻止角膜穿孔的进展。尝试用角膜胶密封穿孔失败,导致决定进行PK。手术期间,角膜组织进行活检和培养以确定病原体。在PK后,角膜培养显示了C. parapsilosis的生长,证实了真菌感染的性质。然后患者重新开始局部使用伏立康唑,延长疗程7个月。在此期间,患者在诊所受到密切监测和随访。幸运的是,在此期间没有真菌病变复发。据我们所知,文献中尚未报道常规白内障手术后由旁锥状角膜炎引起穿孔性角膜溃疡的病例。我们的病人经历了以复发性炎症为特征的术后并发症,这是用强效和频繁的局部类固醇治疗。这种治疗掩盖了潜在的真菌感染,并导致角膜穿孔。最终,患者接受了成功的PK手术以去除感染性病灶,随后延长了7个月的局部伏立康唑疗程。未见病变复发。因此,对于白内障手术后出现迟发性、持续性炎症和透明角膜切口处出现白色斑块的患者,临床医生应警惕真菌性角膜炎,特别是傍角膜炎。PK联合局部抗真菌药物延长术后治疗被证明是一种有效的策略,以管理角膜穿孔引起的斜锥虫角膜炎。
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Case Report of Candida Parapsilosis Keratitis After Cataract Surgery Leading to Corneal Perforation
The objective of this study was to report and document a rare case of Candida parapsilosis keratitis that occurred following a routine clear corneal incision cataract surgery, ultimately resulting in a perforated corneal ulcer and subsequent need for a penetrating keratoplasty (PK). By presenting this case, the study aims to contribute to the existing literature and raise awareness about the potential risk of C. parapsilosis keratitis as a complication of cataract surgery. In this case report, we describe the presentation and management of a rare fungal infection following routine cataract extraction in an 80-year-old male patient. The patient initially received treatment for suspected endophthalmitis and bacterial keratitis but experienced worsening symptoms, including a small corneal perforation. Upon referral to the clinic, the patient exhibited a fluffy stromal infiltrate near the cataract wound site, an epithelial defect, and a hypopyon. Treatment with compounded topical 1% voriconazole was initiated but did not prevent the progression of the corneal perforation. Attempts to seal the perforation with corneal glue were unsuccessful, leading to the decision to perform a PK. During the surgery, corneal tissue was biopsied and cultured to identify the causative agent. Following PK, the corneal cultures revealed the growth of C. parapsilosis, confirming the fungal nature of the infection. The patient was then reinitiated on topical voriconazole for a prolonged course of 7 months. Throughout this period, the patient was closely monitored and followed up in the clinic. Fortunately, there were no recurrences of the fungal lesion during this time. No prior cases of a perforated corneal ulcer resulting from C. parapsilosis keratitis after routine cataract surgery have been reported in the literature to our knowledge. Our patient experienced postoperative complications characterized by recurrent inflammation, which was treated with potent and frequent topical steroids. This treatment masked the underlying mycotic infection and contributed to corneal perforation. Ultimately, the patient underwent a successful PK procedure to remove the infectious nidus, followed by an extended 7-month course of topical voriconazole. No recurrence of the lesion was observed. Therefore, clinicians should be vigilant for mycotic keratitis, specifically C. parapsilosis, in patients who display late-onset, persistent inflammation and white plaques at the clear corneal incision site after cataract surgery. The combination of PK and an extended postoperative treatment with topical antifungal agents proves to be an effective strategy for managing corneal perforations caused by C. parapsilosis keratitis.
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