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穿透性角膜移植术后黄曲霉角膜炎

Aspergillus flavus Keratitis After Penetrating Keratoplasty.

作者信息

Karagiannidou Zoi, Mikropoulos Dimitrios, Boboridis Kostas G

机构信息

Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki, GRC.

1st Department of Ophthalmology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, GRC.

出版信息

Cureus. 2025 Jul 29;17(7):e88985. doi: 10.7759/cureus.88985. eCollection 2025 Jul.

Abstract

Fungal keratitis is a rare but severe complication following penetrating keratoplasty (PKP). We report the clinical course, rapid deterioration, and management of a case of keratitis occurring three months after PKP. A 69-year-old woman with Fuchs' endothelial dystrophy developed pseudophakic bullous keratopathy following cataract surgery. She underwent an uneventful PKP. At two months postoperatively, the graft remained clear with a visual acuity of 2/10. Three months after keratoplasty, the patient presented with pain, redness, mucopurulent discharge, and decreased vision. Slit-lamp examination revealed graft haze with a central epithelial defect, stromal infiltrates, and striae that rapidly progressed into the adjacent recipient cornea. Corneal scrapings were obtained for direct microscopic examination and culture, which revealed septate fungal filaments identified as . Both the donor corneoscleral rim and the recipient corneal tissue were cultured at the time of surgery, and all cultures returned negative for fungal growth. Considering the negative donor cultures, the delayed onset of infection, and the presence of a persistent epithelial defect, the infection was most consistent with a postoperative superinfection rather than a donor-transmitted source. Intensive topical voriconazole and amphotericin B, along with systemic voriconazole, were initiated. Antifungal susceptibility testing was not performed due to the urgent need to initiate empirical therapy following the identification of fungal filaments on direct microscopy and rapid clinical deterioration. Despite aggressive antifungal therapy, the infection progressed, leading to graft melting and corneal perforation. The patient underwent therapeutic PKP, open sky vitrectomy, and removal of the posterior chamber intraocular lens (PC-IOL). Following the removal of the PC-IOL intraoperatively, the patient remained aphakic. Postoperatively, there was no recurrence of infection, and best-corrected visual acuity (BCVA) stabilized at 6/10 with aphakic spectacle correction. This case highlights the virulence of and the challenges in managing post-keratoplasty fungal keratitis, especially when predisposing factors such as persistent epithelial defect and corticosteroid use are present. Early diagnosis and prompt medical and surgical intervention are critical to preserving ocular integrity.

摘要

真菌性角膜炎是穿透性角膜移植术(PKP)后一种罕见但严重的并发症。我们报告了1例PKP术后3个月发生的角膜炎的临床病程、病情迅速恶化情况及治疗过程。一名69岁患有富克斯内皮营养不良的女性在白内障手术后发生了人工晶状体大泡性角膜病变。她接受了顺利的PKP手术。术后两个月,移植片保持透明,视力为2/10。角膜移植术后3个月,患者出现疼痛、眼红、黏液脓性分泌物及视力下降。裂隙灯检查发现移植片有混浊,中央上皮缺损,基质浸润,条纹迅速蔓延至相邻的受体角膜。获取角膜刮片进行直接显微镜检查和培养,发现有分隔的真菌丝,鉴定为 。手术时对供体角膜巩膜缘和受体角膜组织均进行了培养,所有培养结果均为真菌生长阴性。考虑到供体培养阴性、感染延迟发生以及持续上皮缺损的存在,感染最符合术后二重感染而非供体传播来源。开始强化局部应用伏立康唑和两性霉素B,同时全身应用伏立康唑。由于在直接显微镜下发现真菌丝并出现迅速的临床恶化后急需开始经验性治疗,未进行抗真菌药敏试验。尽管进行了积极的抗真菌治疗,感染仍进展,导致移植片溶解和角膜穿孔。患者接受了治疗性PKP、开放式玻璃体切除术及取出后房型人工晶状体(PC-IOL)。术中取出PC-IOL后,患者仍无晶状体。术后,感染未复发,最佳矫正视力(BCVA)通过无晶状体眼镜矫正稳定在6/10。该病例突出了 的毒力以及角膜移植术后真菌性角膜炎治疗中的挑战,尤其是当存在持续上皮缺损和使用皮质类固醇等易感因素时。早期诊断以及及时的药物和手术干预对于保护眼的完整性至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/211c/12393135/e228c4b95577/cureus-0017-00000088985-i01.jpg

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