先天性眼眶淋巴管瘤：20 岁女性患者病例报告及文献复习

Congenital orbital lymphangioma in a 20-years old girl a case report and review of literature.

机构信息

Department of Radiology, National Organ Transplant Centre, Central Hospital, Tripoli, Libya.

出版信息

Libyan J Med. 2009 Dec 1;4(4):162-3. doi: 10.4176/090713.

DOI:10.4176/090713

PMID:21483541

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3066740/

Abstract

We report a case of a 20-year-old girl who presented to the out-patients' department with congenital, progressive unilateral proptosis and reduced vision. Ultrasound, computed tomography (CT) scan and magnetic resonance imaging (MRI) were performed. Diagnosis of orbital lymphangioma was made on imaging. Authors highlight the crucial role of imaging in diagnosis and to plan therapeutic approach. This case is reported because of its extreme rarity and unusual presentation.

摘要

我们报告了一例 20 岁女孩，因先天性、进行性单侧眼球突出和视力下降到门诊就诊。进行了超声、计算机断层扫描（CT）和磁共振成像（MRI）检查。影像学诊断为眼眶淋巴管瘤。作者强调了影像学在诊断和制定治疗方法中的关键作用。本病例报告的原因是其极其罕见和异常的表现。