Stahl-Hoffmann V D, Gräf M, Cesnulis E, Schuknecht B, Lorenz B
Klinik und Poliklinik für Augenheilkunde, Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen, Friedrichstraße 18, 35385, Gießen, Deutschland.
Neurochirurgie Zürich, Klinik Hirslanden, Kappelistrasse 35, 8032, Zürich, Schweiz.
Ophthalmologe. 2016 Jun;113(6):514-6. doi: 10.1007/s00347-015-0131-6.
We report a case of symptomatic ecchordosis physaliphora (EP) in a 34-year-old woman who presented with progressive diplopia due to palsy of the left sixth cranial nerve. Repeated magnetic resonance imaging (MRI) disclosed typical characteristics of a congenital EP lesion with compression of the left abducens nerve presumably because of a secondary herniation of the arachnoid mater. We performed an augmenting combined recess resect procedure on the left eye. No progression of the lesion was observed over a period of 5 years. For differential diagnostics an EP has to be distinguished from skull base tumors, such as chordoma and chondrosarcoma.
我们报告一例34岁女性有症状的泡状脊索瘤(EP),该患者因左侧第六颅神经麻痹出现进行性复视。反复的磁共振成像(MRI)显示先天性EP病变的典型特征,左侧展神经受压可能是由于蛛网膜继发性疝出所致。我们对左眼进行了增强联合隐窝切除手术。在5年的时间里未观察到病变进展。为了进行鉴别诊断,EP必须与颅底肿瘤,如脊索瘤和软骨肉瘤相区分。