Honda E, Uegaki M, Shojima K, Hayashi T, Shigemori M, Kuramoto S
No Shinkei Geka. 1981 Dec;9(13):1527-33.
A case of arterio-venous malformation (AVM) at the right parietal area in association with agenesis of the left internal carotid artery (ICA) is described. A 27-year-old male complained of severe headache and vomiting on September 27th in 1980. He lost his consciousness and became stuporous within several minutes after the ictus. He was then transferred to Kurume University Hospital. On admission, he was semicomatose, anisocoria and left hemiparesis marked in the lower limbs, and bilateral Babinski reflex were noted. A emergency CT scan revealed a round high density area suggesting intracerebral hematoma at the right parieto-occipital area. Right retrograde brachial angiography was then performed which showed a small AVM at the right parietal lobe mainly fed by the right posterior parietal arterial branch, and drained into the superior sagittal sinus, via the subcortial veins. Left MCA bilateral PCA and SCA also were demonstrated on the angiogram. The angiogram suggested on abnormality of the Willis ring. Emergency operation fro the small AVM associated with intracerebral hematoma was then performed. The AVM was sufficiently removed and approximately 80 gr. of intracerebral clots were also evacuated completely. Histological examination indicated a typical small AVM. The postoperative course was uneventful. Left CAG performed by seldinger method from the femoral artery after the operation showed no demonstration of the left ICA. the left common carotid artery was terminated as the external carotid artery without carotid bifurcation at the neck. The left ophthalmic artery was fed by the meningeal artery of the internal maxillary artery. Left vertebrobasilar system was normal. From an angiogram, the agenesis of the left ICA was most suspected. An agenesis of ICA was uncommon among the literature in which there was no case with this anomaly associated with cerebral AVM. The embryological consideration about this case was mainly discussed.
本文描述了一例右侧顶叶动静脉畸形(AVM)合并左侧颈内动脉(ICA)缺如的病例。一名27岁男性于1980年9月27日出现严重头痛和呕吐。发病后几分钟内,他失去意识并陷入昏迷。随后被转至久留米大学医院。入院时,他处于半昏迷状态,双侧瞳孔不等大,下肢左侧偏瘫明显,双侧巴氏征阳性。急诊CT扫描显示右侧顶枕叶区域有一个圆形高密度区,提示脑内血肿。随后进行了右侧逆行肱动脉血管造影,显示右侧顶叶有一个小AVM,主要由右侧顶叶后动脉分支供血,并通过皮质下静脉引流至上矢状窦。血管造影还显示了左侧大脑中动脉、双侧大脑后动脉和小脑上动脉。血管造影提示Willis环异常。随后对与脑内血肿相关的小AVM进行了急诊手术。AVM被充分切除,约80克脑内血凝块也被完全清除。组织学检查显示为典型的小AVM。术后病程顺利。术后经股动脉采用Seldinger法进行的左侧脑血管造影(CAG)显示未发现左侧ICA。左侧颈总动脉在颈部未形成颈动脉分叉,仅终止于颈外动脉。左侧眼动脉由上颌内动脉的脑膜动脉供血。左侧椎基底系统正常。从血管造影来看,最怀疑左侧ICA缺如。ICA缺如在文献中并不常见,且尚无与脑AVM相关的此类异常病例。本文主要讨论了该病例的胚胎学相关问题。