Infectious crystalline keratopathy

被引:26
|
作者
Porter, Ashley J. [1 ]
Lee, Graham A. [1 ,2 ,3 ]
Jun, Albert S. [4 ]
机构
[1] City Eye Ctr, Brisbane, Qld, Australia
[2] Univ Queensland, Brisbane, Qld, Australia
[3] Mater Hlth Serv, Brisbane, Qld, Australia
[4] Wilmer Eye Inst, Baltimore, MD 21287 USA
关键词
nfectious crystalline keratopathy; keratoplasty; biofilm; keratitis; COLLAGEN CROSS-LINKING; BACTERIAL BIOFILMS; MYCOBACTERIUM-ABSCESSUS; KERATITIS; COLONIZATION; KERATOCONUS; DISRUPTION; RESISTANCE; MICROSCOPY; MANAGEMENT;
D O I
10.1016/j.survophthal.2017.10.008
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Infectious crystalline keratopathy was first reported by Gorovoy and colleagues in 1983 when they identified bacteria colonizing a cornea after a penetrating keratoplasty. Subsequent cases have elaborated on the organisms responsible and the management outcomes. Patients present with a white or gray branching opacity originating from an epithelial defect, commonly after a penetrating keratoplasty. Local immunosuppression contributes to the quiescent nature and the limited inflammatory response associated with infectious crystalline keratopathy. Diagnosis of the infective pathogens may be difficult, with a corneal scraping often being too superficial to obtain an adequate specimen. A biofilm is present that advantages microorganism survival, reduces antibiotic bioavailability, and inhibits diagnostic microbial detection. Treatment begins with topical anti-microbials, initially broad spectrum and then targeted to microorganism sensitivity. Adjunctive therapies to enhance the efficacy of treatment include disruption of the microorganism biofilm by laser, intrastromal antibiotics, and keratectomy. In recalcitrant cases, or where corneal scarring ensues, corneal transplantation is required. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:480 / 499
页数:20
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