Department of Ophthalmology, National Cheng-Kung University College of Medicine and Hospital, Tainan, Taiwan.
Cornea. 2012 Apr;31(4):442-6. doi: 10.1097/ICO.0b013e31823f091a.
To study the safety and efficacy of treating early-stage Acanthamoeba keratitis (AK) with 20% alcohol-assisted epithelial debridement.
Four consecutive patients (2 wearing orthokeratology lenses and 2 wearing soft contact lenses) presented with pseudodendrites, radial keratoneuritis, and epithelial irregularities. Using a technique similar to laser-assisted subepithelial keratomileusis, we performed alcohol-assisted full-thickness debridement of the corneal epithelium and sent portions for smears, histopathologic and ultrastructural examinations, and culture for evidence of Acanthamoeba. Patients were then started on topical propamidine isethionate and 0.02% polyhexamethylene biguanide.
Immediately after debridement, minimal underlying anterior stromal infiltrate or haze was seen. Dosages of antiamoebic agents were tapered as corneal defects reepithelialized (in 1-3 weeks) with no evidence of post-debridement corneal infection. At the final follow-up, 1 cornea was transparent and the other 3 corneas had very faint subepithelial haze. Cultures of all epithelial debridement specimens yielded Acanthamoeba trophozoites and cysts, and histopathologic and electron microscopic examinations revealed Acanthamoeba organisms within corneal epithelial layers.
Alcohol-assisted epithelial debridement facilitates detachment of the full-thickness corneal epithelial layer in a controlled manner and seems to be effective in the treatment of early-stage AK. Unlike the fragile fragmented specimens obtained by mechanical scraping without alcohol soaking, epithelial sheets detached easily and the architectures were well preserved, permitting histopathologic and ultrastructural examinations. Most importantly, 20% alcohol-assisted epithelial debridement did not prevent culturing of Acanthamoeba from the removed epithelial specimens.
研究 20%酒精辅助性上皮清创术治疗早期棘阿米巴角膜炎(AK)的安全性和有效性。
连续 4 例(2 例佩戴角膜塑形镜,2 例佩戴软性隐形眼镜)患者出现假树枝状、放射状角膜神经病变和上皮不规则。采用类似于激光辅助性上皮下角膜磨镶术的技术,我们对角膜上皮进行了酒精辅助性全层清创,并对部分组织进行了涂片、组织病理学和超微结构检查以及培养以寻找棘阿米巴的证据。然后,患者开始接受丙脒腙和 0.02%聚六亚甲基双胍滴眼。
清创后立即出现少量基底前基质浸润或混浊。随着角膜缺损的再上皮化(1-3 周),抗阿米巴药物的剂量逐渐减少,没有证据表明清创后角膜感染。在最终随访时,1 只眼的角膜透明,另外 3 只眼的角膜有非常轻微的上皮下混浊。所有上皮清创标本的培养均产生棘阿米巴滋养体和包囊,组织病理学和电子显微镜检查显示棘阿米巴原虫存在于角膜上皮层内。
酒精辅助性上皮清创术以可控的方式促进全层角膜上皮的脱离,似乎对早期 AK 有效。与没有酒精浸泡的机械刮除获得的脆弱、破碎的标本不同,上皮片很容易脱离,并且结构保存完好,允许进行组织病理学和超微结构检查。最重要的是,20%酒精辅助性上皮清创术并未阻止从去除的上皮标本中培养出棘阿米巴。