Lu C Y, Hou J W, Wang P J, Chiu H H, Wang T R
Department of Pediatrics, National Taiwan University Hospital, Taipei.
Pediatr Neurol. 1996 Sep;15(2):159-62. doi: 10.1016/0887-8994(96)00117-8.
A patient with homocystinuria presenting with fatal cerebral infarction that resulted from left common carotid artery occlusion is reported. This 13-year-old, healthy and intelligent girl presented with progressive cerebral infarction. Angiography revealed total occlusion of the left common carotid artery and stenosis of the right common carotid artery. Distal stenosis of bilateral vertebral arteries was also observed. Initially Takayasu arteritis with unusual manifestation was considered. However, later investigations revealed homocystinuria was the underlying cause. The sudden onset of fatal stroke as the initial clinical presentation of homocystinuria, as observed in this previous healthy teenager, is noteworthy. We suggest metabolic screening for homocystinuria when treating a patient with unusual vascular lesions.
本文报道了一名患有同型胱氨酸尿症的患者,该患者因左颈总动脉闭塞导致致命性脑梗死。这名13岁、健康且聪明的女孩出现了进行性脑梗死。血管造影显示左颈总动脉完全闭塞,右颈总动脉狭窄。还观察到双侧椎动脉远端狭窄。最初考虑为表现不寻常的高安动脉炎。然而,后来的检查显示同型胱氨酸尿症是根本原因。正如在这名先前健康的青少年中所观察到的,同型胱氨酸尿症以致命性中风作为首发临床表现突然起病,这一点值得注意。我们建议在治疗有不寻常血管病变的患者时,对同型胱氨酸尿症进行代谢筛查。