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一种矫正弗雷泽综合征隐眼畸形的手术策略。

A surgical strategy for the correction of Fraser syndrome cryptophthalmos.

作者信息

Saleh George M, Hussain Badrul, Verity David H, Collin J Richard O

机构信息

Oculoplastic Service, Moorfields Eye Hospital, City Road, London, United Kingdom.

出版信息

Ophthalmology. 2009 Sep;116(9):1707-1712.e1. doi: 10.1016/j.ophtha.2009.05.018. Epub 2009 Jul 29.

Abstract

PURPOSE

To describe a systematic approach for managing the structural adnexal anomalies encountered in Fraser syndrome, a multisystem, autosomal recessive condition associated with cryptophthalmos.

DESIGN

Retrospective, noncomparative, interventional case series.

PARTICIPANTS

All patients with Fraser syndrome-related cryptophthalmos managed at a Moorfields Eye Hospital during a 23-year period between 1984 and 2007.

METHODS

All patients' clinical records were reviewed. The age of the patient at presentation, sex, ethnic origin, parental consanguinity, associated systemic features, length of follow-up, and surgical interventions were recorded.

MAIN OUTCOME MEASURES

The sequence of surgical procedures performed for the different morphologic cryptophthalmos subtypes, postoperative visual acuity, and corneal survival.

RESULTS

The study includes 13 eyes of 7 patients. Cryptophthalmos was complete in 3 eyes and abortive in 10 eyes; no cases of incomplete cryptophthalmos were encountered in this series. The aim of surgical intervention in the latter was to optimize visual potential. Surgical steps included dissection of corneal adhesions from keratinized cornea, mucous membrane graft, Mustarde eyelid switch flap with subsequent division, and further lower lid augmentation as required (n = 10). For complete cryptophthalmos, surgery was recommended if cosmetic improvement was sought and enough tissue remained after any repair of abortive cryptophthalmos in the fellow eye. Surgery in these cases involved the creation of fornices, with subsequent upper and lower lid reconstruction with local skin/muscle flaps (n = 1). Postoperative acuities ranged from perception of light to 20/200. Good outcomes in terms of corneal health were achieved in 6 of the 10 eyes operated on for incomplete cryptophthalmos.

CONCLUSIONS

Although Fraser syndrome is rare, the periocular surgical management of these complex cases may be planned using a systematic approach as described in this study, which is the largest such series to date.

FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

摘要

目的

描述一种系统性方法,用于处理在弗雷泽综合征中遇到的附属器结构异常,弗雷泽综合征是一种与隐眼畸形相关的多系统常染色体隐性疾病。

设计

回顾性、非对照、干预性病例系列研究。

参与者

1984年至2007年期间在摩尔菲尔德眼科医院接受治疗的所有患有与弗雷泽综合征相关隐眼畸形的患者。

方法

回顾所有患者的临床记录。记录患者就诊时的年龄、性别、种族、父母近亲关系、相关的全身特征、随访时间以及手术干预情况。

主要观察指标

针对不同形态学类型的隐眼畸形亚型所进行的手术步骤顺序、术后视力以及角膜存活情况。

结果

该研究纳入了7例患者的13只眼。隐眼畸形完全型3只眼,不完全型10只眼;本系列未遇到不完全隐眼畸形病例。对于不完全型隐眼畸形,手术干预的目的是优化视觉潜能。手术步骤包括从角化角膜分离角膜粘连、黏膜移植、Mustarde眼睑转位皮瓣及后续分离,并根据需要进一步进行下睑增大术(n = 10)。对于完全型隐眼畸形,如果寻求美容改善且对侧眼不完全型隐眼畸形修复后仍有足够组织,则建议进行手术。这些病例的手术包括穹窿的创建,随后用局部皮肤/肌肉皮瓣进行上睑和下睑重建(n = 1)。术后视力范围从光感至20/200。在接受不完全型隐眼畸形手术的10只眼中,有6只眼在角膜健康方面取得了良好效果。

结论

尽管弗雷泽综合征罕见,但这些复杂病例的眼周手术管理可采用本研究中描述的系统性方法进行规划,这是迄今为止最大的此类系列研究。

财务披露

作者对本文中讨论的任何材料均无所有权或商业利益。

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