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两例广泛角膜巩膜疾病患者行保留房角的角膜巩膜成形术。

Corneoscleroplasty with maintenance of the angle in two cases of extensive corneoscleral disease.

作者信息

Burk R O, Joussen A M

机构信息

Department of Ophthalmology, University of Heidelberg, Germany.

出版信息

Eye (Lond). 2000 Apr;14 ( Pt 2):196-200. doi: 10.1038/eye.2000.53.

Abstract

PURPOSE

We report a 2 year follow-up in two patients after corneoscleroplasty.

METHOD

Using lamellar corneoscleral dissection to maintain the drainage angle and its function, we performed a 14 mm allograft corneoscleroplasty in 2 eyes. For surgical treatment in both cases a 9.5 mm corneal button was excised from the recipient after peritomy and scleral lamellar preparation up to 14 mm. A 14 mm donor button was inserted and held in place with multiple Prolene sutures. One eye presented with a large perforating corneal ulcer after herpetic keratitis in a patient with recurrent rheumatoid uveitis associated with rubeosis iridis. The second eye had had a penetrating keratoplasty for keratoconus 30 years previously and presented with decompensating keratoglobus. Immune suppression was performed with systemic cyclosporin A and additional steroids when required.

RESULTS

Both patients had a clear graft at the last follow-up visit and visual acuity was improved to a best corrected visual acuity of 0.6. Intraocular pressure in the keratoglobus eye was maintained at 6 mmHg without treatment, whereas the second case required continuing treatment with systemic acetazolamide because of neovascular glaucoma. The anterior chamber angles remained open in both patients. Contact lenses were helpful in the prevention of epithelial irregularities and defects. Both patients had an episode of immunological graft reaction which was reversed by immunosuppressive treatment. Phacoemulsification with intraocular lens implantation, which was performed 2 years after transplantation in the keratoglobus eye, did not affect the graft clarity or cause rejection episodes.

CONCLUSION

Our results using corneoscleroplasty have been encouraging in severe destructive corneal disease.

摘要

目的

我们报告两例患者角膜巩膜移植术后的2年随访情况。

方法

采用板层角膜巩膜剥离术以维持房角及其功能,我们对2只眼进行了14毫米同种异体角膜巩膜移植术。在两例病例的手术治疗中,在球结膜切开术和巩膜板层制备至14毫米后,从受体眼中切除9.5毫米的角膜纽扣。插入一个14毫米的供体纽扣,并用多根普理灵缝线固定到位。一只眼在患有复发性类风湿性葡萄膜炎伴虹膜红变的患者中,疱疹性角膜炎后出现巨大穿孔性角膜溃疡。另一只眼30年前因圆锥角膜接受过穿透性角膜移植术,现出现角膜膨隆失代偿。必要时使用全身性环孢素A和额外的类固醇进行免疫抑制。

结果

在最后一次随访时,两名患者的移植片均保持透明,最佳矫正视力提高到了0.6。角膜膨隆眼的眼压未经治疗维持在6 mmHg,而第二例因新生血管性青光眼需要继续使用全身性乙酰唑胺治疗。两名患者的前房角均保持开放。隐形眼镜有助于预防上皮不规则和缺损。两名患者均发生了一次免疫性移植反应,通过免疫抑制治疗得到逆转。在角膜膨隆眼移植2年后进行的白内障超声乳化联合人工晶状体植入术,未影响移植片的清晰度或引发排斥反应。

结论

我们使用角膜巩膜移植术治疗严重破坏性角膜疾病的结果令人鼓舞。

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