Amin Osama Sm, Shwani Sa'ad Seud, Zangana Hero M, Ameen Nawa A
Department of Neurology, Sulaimaniya General Teaching Hospital, Sulaimaniya City, Iraq.
J Med Case Rep. 2011 Jul 25;5:324. doi: 10.1186/1752-1947-5-324.
Bilateral ischemic infarction involving the corpus striatum is a rare event which usually results from global cerebral hypoxia, intoxications, and drug abuse.
We report a 28 year old Caucasian woman who presented with progressive obtundation and later development of severe expressive dysphasia and Parkinsonism after sustaining ischemic stroke of both corpora striata. Hemorrhagic transformation developed on day four of admission.
This is a rare case of bilateral basal ganglia infarction with hemorrhagic transformation in a young patient. Our patient's work up did not reveal any cause behind this stroke; however, advanced investigations (such as genetic testing and conventional angiography) were not done. The damage resulted in motor dysphasia and Parkinsonism. Neither dystonia nor other involuntary movements developed, and cognitive function was not assessed because of the language disorder.
双侧纹状体缺血性梗死是一种罕见事件,通常由全脑缺氧、中毒和药物滥用引起。
我们报告一名28岁的白种女性,她在双侧纹状体发生缺血性中风后出现进行性意识模糊,随后发展为严重的表达性失语和帕金森综合征。入院第4天出现出血性转化。
这是一例年轻患者双侧基底节梗死伴出血性转化的罕见病例。我们患者的检查未发现此次中风背后的任何病因;然而,未进行进一步检查(如基因检测和传统血管造影)。损伤导致运动性失语和帕金森综合征。既未出现肌张力障碍也未出现其他不自主运动,并且由于语言障碍未评估认知功能。