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睑裂狭小综合征患者的先天性无泪症。

Congenital alacrima in a patient with blepharophimosis syndrome.

作者信息

Athappilly Geetha K, Braverman Rebecca Sands

机构信息

The University of Colorado at Denven and Health Services Center, Rocky Mountain Lions Eye Institute, Denver, CO 80045, USA.

出版信息

Ophthalmic Genet. 2009 Mar;30(1):37-9. doi: 10.1080/13816810802452176.

Abstract

PURPOSE

To report a case of congenital alacrima in a patient with Blepharophimosis Syndrome (BPES).

METHODS

Case report of a 9-month-old female who presented with severe dry eyes. Further investigation revealed bilateral absence of lacrimal glands confirmed by CT. This unique case and its management are discussed.

RESULTS

Conservative management with artificial tears and ointment did not treat the ocular surface dryness. A combination of aggressive lubrication with surgical occlusion of the lower lid punctums was required to improve the corneal surface.

CONCLUSION

BPES can be associated with many ophthalmic and facial abnormalities. Review of the pubmed literature, reveals this is the first reported case of alacrima and BPES. Patient with alacrima have severe ocular surface dryness, which requires aggressive and life long lubrication and tear supplementation.

摘要

目的

报告一例患有睑裂狭小综合征(BPES)的先天性无泪症患者。

方法

对一名9个月大出现严重干眼症状的女性患者进行病例报告。进一步检查发现CT证实双侧泪腺缺失。讨论了这一独特病例及其治疗方法。

结果

使用人工泪液和眼膏的保守治疗未能改善眼表干燥状况。需要积极润滑并手术封闭下睑泪点以改善角膜表面情况。

结论

BPES可伴有多种眼科和面部异常。查阅PubMed文献发现,这是首例报道的无泪症与BPES并存的病例。无泪症患者存在严重的眼表干燥,需要积极且终身的润滑和补充泪液治疗。

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