Suzuki Kosuke, Ataka Takuya, Kimura Noriyuki, Matsubara Etsuro
Department of Neurology, Oita University Faculty of Medicine, Japan.
Intern Med. 2024 Sep 15;63(18):2547-2550. doi: 10.2169/internalmedicine.2681-23. Epub 2024 Feb 12.
We herein report the a 42-year-old man with early-onset cerebral amyloid angiopathy (CAA) and a history of traumatic brain injury and neurosurgery in childhood. Computed tomography revealed cognitive impairment and recurrent lobar intracerebral hemorrhaging. Magnetic resonance imaging indicated cerebral microbleeds, and Pittsburgh compound B positron emission tomography detected brain amyloid deposition, mainly in the region of trauma and occipital lobes. Interestingly, the patient had no genetic predispositions or relevant family history. This case suggests that a single traumatic brain injury or neurosurgery in childhood can cause early-onset CAA.
我们在此报告一名42岁男性,患有早发性脑淀粉样血管病(CAA),童年时有创伤性脑损伤和神经外科手术史。计算机断层扫描显示认知障碍和复发性脑叶脑出血。磁共振成像显示脑微出血,匹兹堡化合物B正电子发射断层扫描检测到脑淀粉样蛋白沉积,主要位于创伤区域和枕叶。有趣的是,该患者没有遗传易感性或相关家族史。该病例表明,童年时期的单次创伤性脑损伤或神经外科手术可导致早发性CAA。