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[1例表现为大脑后动脉-后交通动脉瘤破裂的、与双侧颈内动脉发育不全相关的颈-小脑上动脉吻合病例]

[A case of carotid superior cerebellar artery anastomosis associated with bilateral hypoplasia of the internal carotid artery represented as the rupture of posterior cerebral artery-posterior communicating artery aneurysm].

作者信息

Okuno T, Nishiguchi T, Hayashi S, Miyamoto K, Terashita T, Itakura T, Moriwaki H, Komai N

机构信息

Department of Neurological Surgery, Wakayama Medical College, Japan.

出版信息

No Shinkei Geka. 1988 Sep;16(10):1211-7.

PMID:3060752
Abstract

A rare case of a variant type of the persistent primitive trigeminal artery associated with bilateral hypoplasia of the internal carotid artery was reported. Left common carotid arteriography revealed a thin left internal carotid artery terminated at the ophthalmic artery. Right common carotid arteriography showed that a narrow internal carotid artery gave off several fine vessels to the cavernous portion, and terminated at the right superior cerebellar artery via the prominent persistent primitive trigeminal artery (PTA). Supraclinoid portions of the bilateral internal carotid arteries were not able to be found. Eventually the entire cerebral hemisphere was supplied by the vertebrobasilar system via the posterior communicating artery. The narrowed supraclinoid portion of the left internal carotid artery was confirmed by surgery of the left posterior cerebellar artery-posterior communicating artery aneurysm. This case may provide an important suggestion about the mechanism of the persistence of the primitive trigeminal artery. In an embryo, at the stage of 5-6mm embryo in size, the posterior communicating artery begins to develop and then PTAs begin to dwindle. If the C1- or C2- portion of the internal carotid artery is gradually occluded, the forebrain, which has to be supplied by the internal carotid system, must be supplied retrogradely by the basilar system via the posterior communicating artery. At this stage, however, the vertebral artery has not developed enough to supply the entire central nervous system. Therefore, the PTA can not regress and this results in the postnatal persistence of the primitive trigeminal artery.

摘要

报道了一例罕见的持续性原始三叉动脉变异型病例,该病例伴有双侧颈内动脉发育不全。左颈总动脉造影显示左颈内动脉纤细,止于眼动脉。右颈总动脉造影显示,狭窄的颈内动脉向海绵窦段发出数条细小血管,并通过明显的持续性原始三叉动脉(PTA)止于右小脑上动脉。双侧颈内动脉鞍上段未发现。最终,整个大脑半球由椎基底系统通过后交通动脉供血。左小脑后动脉-后交通动脉瘤手术证实了左颈内动脉鞍上段狭窄。该病例可能为原始三叉动脉持续存在的机制提供重要线索。在胚胎期,胚胎大小为5-6mm时,后交通动脉开始发育,然后PTA开始萎缩。如果颈内动脉的C1或C2段逐渐闭塞,必须由颈内动脉系统供血的前脑就必须由基底系统通过后交通动脉逆行供血。然而,在这个阶段,椎动脉尚未发育到足以供应整个中枢神经系统。因此,PTA不能退化,这导致了出生后原始三叉动脉的持续存在。

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