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成人先天性单侧泪点缺如合并泪囊膨出

Dacryocystocele with congenital unilateral lacrimal puncta agenesis in an adults.

作者信息

Han Ba Leun, Shin Ho Seong

机构信息

Department of Plastic and Reconstructive Surgery, College of Medicine, Soonchunhyang University, Bucheon, Republic of Korea.

出版信息

J Craniofac Surg. 2013 Jul;24(4):1242-3. doi: 10.1097/SCS.0b013e31828b717b.

Abstract

Unilateral agenesis of the lacrimal puncta and enlargement of the lacrimal canal in adults are rare anatomic variants. We herein report a case of a 34-year-old woman with a unilateral dacryocystocele and lacrimal puncta agenesis. The patient had a long history of epiphora and visited the author's clinic for evaluation of a mass in her right medial canthal area that had been growing for the last 2 months. This article reports the results of the author's physical examinations, magnetic resonance imaging findings, and surgical treatment comprising dacryocystorhinostomy with silicone tubes. Six months after surgery, the patient's symptoms improved.

摘要

成人单侧泪点缺如及泪管扩大是罕见的解剖变异。我们在此报告一例34岁女性,患有单侧泪囊膨出及泪点缺如。该患者有长期溢泪史,因右内眦区肿物2个月来作者诊所就诊,肿物一直在生长。本文报告了作者的体格检查结果、磁共振成像表现以及包括硅胶管泪囊鼻腔吻合术在内的手术治疗情况。术后6个月,患者症状改善。

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