Dziewas R, Schilling M, Fallenberg E M, Allroggen A, Lüdemann P, Henningsen H
Klinik und Poliklinik für Neurologie, Universitätsklinikum Münster.
Nervenarzt. 2003 Feb;74(2):172-4. doi: 10.1007/s00115-002-1461-6.
The megadolichobasilar artery is a rare vascular disease, which usually becomes apparent either due to cerebral ischemia or due to compression of the brainstem or the cranial nerves, thereby leading to a large variety of neurological symptoms. We report on a patient who suffered a sudden right-sided deafness accompanied by vertigo and vomiting. Initially, an idiopathic sensorineural hearing loss was diagnosed and later on, after no improvement took place in spite of conservative therapy, a rupture of the round window membrane was suspected. Two weeks after the first symptoms had occurred the patient developed a hemiparesis on the left side.Radiology disclosed a dilated and partially thrombosed basilar artery as well as a paramedian pontine infarction. We therefore assumed that the patient's symptoms had been caused by thrombotic occlusion of the labyrinthine artery and several rami ad pontem. The article reviews the great variety of clinical symptoms caused by megadolichobasilar artery and discusses important therapeutic options.
巨长基底动脉是一种罕见的血管疾病,通常因脑缺血或脑干或颅神经受压而显现,从而导致各种各样的神经症状。我们报告了一例患者,其突然出现右侧耳聋并伴有眩晕和呕吐。最初诊断为特发性感音神经性听力损失,后来尽管进行了保守治疗但病情无改善,怀疑是圆窗膜破裂。首次出现症状两周后,患者左侧出现偏瘫。放射学检查显示基底动脉扩张且部分血栓形成,以及脑桥旁正中梗死。因此,我们认为患者的症状是由迷路动脉和数条脑桥支的血栓性闭塞所致。本文回顾了巨长基底动脉引起的多种临床症状,并讨论了重要的治疗选择。