Denovo development of corneal guttae and Fuchs' dystrophy in corneal grafts.

G Alexandrakis, V Filatov, A P Adamis
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引用次数: 0

Abstract

Purpose: To describe two cases of de novo development of corneal guttae and Fuchs' dystrophy in donor tissue following penetrating keratoplasty (PK) for unrelated conditions.

Methods: Two patients underwent PK for keratoconus and a disciform scar secondary to herpes simplex virus. They were followed clinically for a period of 16 and 11 years, respectively. Specular microscopy was used in one patient.

Results: Corneal guttae were first noted 10 years and 4 years following transplantation in the first and second patient, respectively. In both cases, the corneal guttae gradually increased in number, involving the central and temporal portions of the corneal graft There were no corneal guttae present in the host corneal rim or contralateral cornea of either patient.

Conclusions: These cases provide evidence to suggest that some corneas may be genetically predetermined to develop corneal guttae and Fuchs' dystrophy many years before any changes can be clinically detected.

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角膜移植物中角膜瘘管的发育与Fuchs营养不良。
目的:描述两例角膜穿透性角膜移植术(PK)后供体组织中角膜瘘管和Fuchs营养不良的重新发展。方法:2例患者因圆锥角膜和单纯疱疹病毒继发盘状瘢痕行PK治疗。他们分别被临床随访了16年和11年。1例患者采用镜面镜检。结果:第1例和第2例患者分别在移植后10年和4年首次发现角膜瘘管。在这两个病例中,角膜瘘管的数量逐渐增加,累及角膜移植物的中央和颞部。在宿主角膜边缘和对侧角膜中均未发现角膜瘘管。结论:这些病例提供的证据表明,一些角膜可能是基因预先决定的,在临床上发现任何变化之前很多年就会发生角膜瘘和富克斯营养不良。
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