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先天性鼻泪管黏液囊肿:CT评估

Congenital nasolacrimal mucoceles: CT evaluation.

作者信息

Rand P K, Ball W S, Kulwin D R

机构信息

Department of Radiology, Children's Hospital Medical Center, Cincinnati, OH 45229-2899.

出版信息

Radiology. 1989 Dec;173(3):691-4. doi: 10.1148/radiology.173.3.2813773.

Abstract

A congenital nasolacrimal mucocele, a lacrimal sac mucocele with intranasal extension, is an uncommon mass arising in the medial canthal region of the orbit. The authors describe four infants who presented with medial canthal masses and nasal airway obstruction. All underwent computed tomographic (CT) evaluation, which revealed the triad of cystic dilatation of the lacrimal sac, dilatation of the nasolacrimal duct, and an intranasal cystic mass. Appropriate therapy was determined following identification of the intranasal cystic component. Relevant discussions of the embryology, clinical presentation, and the characteristic CT findings of infants with congenital nasolacrimal mucoceles are included.

摘要

先天性鼻泪管黏液囊肿是一种泪囊黏液囊肿并向鼻腔扩展,是一种罕见的肿块,出现在眼眶内眦区域。作者描述了4例以内眦肿块和鼻气道阻塞就诊的婴儿。所有患儿均接受了计算机断层扫描(CT)评估,结果显示泪囊囊性扩张、鼻泪管扩张和鼻内囊性肿块三联征。在确定鼻内囊性成分后确定了适当的治疗方法。文中还包括了对先天性鼻泪管黏液囊肿婴儿的胚胎学、临床表现和特征性CT表现的相关讨论。

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