Iampreechakul Prasert, Lertbutsayanukul Punjama, Wattanasen Yodkwhan, Thiraworawong Thon, Komonchan Surasak, Siriwimonmas Somkiet
Department of Neurosurgery, Prasat Neurological Institute, Bangkok, Thailand.
Department of Neuroradiology, Prasat Neurological Institute, Bangkok, Thailand.
Asian J Neurosurg. 2020 Feb 25;15(1):144-154. doi: 10.4103/ajns.AJNS_317_19. eCollection 2020 Jan-Mar.
We describe a patient with multiple cranial dural arteriovenous fistulas (DAVFs) presenting with thalamic dementia. A 52-year-old man experienced progressive dementia and behavioral change for 1 month. Cranial computed tomography scan and magnetic resonance imaging (MRI) showed bilateral thalamic edema with subsequent hemorrhagic transformation. Cerebral angiography demonstrated multiple cranial DAVFs at the straight sinus and posterior part of the superior sagittal sinus. The symptomatic fistula was the straight sinus DAVF, Cognard Type II a + b, supplied by meningeal branches of the left superior cerebellar artery, the left ascending pharyngeal artery originating from the left occipital artery, and multiple tiny branches of the left occipital artery with retrograde venous drainage into the straight sinus and vein of Galen. In addition, there was probable thrombosis at the middle part of the straight sinus associated with anatomical variation of the dural venous sinuses at the torcular herophili. The patient underwent successfully endovascular treatments in a two-staged embolization using liquid embolic materials. The patient has gradually recovered and could get back to the activities of daily living at home within 2 months. Follow-up MRI of the brain at 6 months revealed nearly complete resolution of the bilateral thalamic congestion. Cerebral angiography, obtained 1 year after endovascular treatment, confirmed complete obliteration of both DAVFs. We also reviewed the literature of thalamic dementia caused by intracranial DAVFs.
我们描述了一名患有多发性硬脑膜动静脉瘘(DAVF)并表现为丘脑痴呆的患者。一名52岁男性出现进行性痴呆和行为改变1个月。头颅计算机断层扫描和磁共振成像(MRI)显示双侧丘脑水肿,随后发生出血性转化。脑血管造影显示在直窦和上矢状窦后部存在多发性硬脑膜动静脉瘘。有症状的瘘为直窦DAVF,Cognard II a + b型,由左小脑上动脉的脑膜支、起源于左枕动脉的左咽升动脉以及左枕动脉的多个微小分支供血,静脉逆向引流至直窦和大脑大静脉。此外,直窦中部可能存在血栓形成,与窦汇处硬脑膜静脉窦的解剖变异有关。该患者成功接受了使用液体栓塞材料的两阶段血管内栓塞治疗。患者逐渐康复,并在2个月内能够恢复在家中的日常生活活动。6个月时的脑部随访MRI显示双侧丘脑充血几乎完全消退。血管内治疗1年后进行的脑血管造影证实两个DAVF均完全闭塞。我们还回顾了由颅内DAVF引起的丘脑痴呆的文献。