胎儿变异大脑后动脉单侧部分重复伴小脑上动脉重复异常起源:病例报告。

IF 1.4 Q3 ANATOMY & MORPHOLOGY
Ehab Mostafa Elzawawy, Mumen Hamdi Al-Mutori, Hadil Salim Al Awaisi, Abdulrahman Abdulrahman Al Dagher, Mustafa Mohamed Allayeth, Hassan Reda Hassan Elsayed
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引用次数: 0

摘要

胚胎颈内动脉和椎基底动脉系统交界处的变异非常罕见,而且与中风的高发病率有关。在尸体解剖过程中,我们首次发现了一例右侧椎动脉发育不良的病例,该病例伴有胎儿部分大脑后动脉(FPCA)右侧 P1 段远端部分重复和双侧小脑上动脉(SCA)重复,其中右侧 SCA 上段起源于 PCA。我们推测,椎基底动脉系统右半部发育不良导致 FPCA 持续存在,右上 SCA 起源异常,以及 PCA P1 段部分重复,这是胚胎期右 PCA 与基底动脉系统之间薄弱吻合的残余。这些复杂的变异给中风的诊断和选择合适的治疗方法带来了巨大的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A unilateral partial duplication of a fetal variant posterior cerebral artery associated with anomalous origin of duplicated superior cerebellar artery: a case report.

Variations at the junction of embryonic internal carotid and vertebrobasilar systems are rare and associated with a high incidence of stroke. During cadaver dissection, we demonstrated for the first time a case of hypoplastic right vertebral artery associated with partial duplication of the distal part of the right P1 segment of a partial fetal posterior cerebral artery (FPCA) and bilateral duplication of superior cerebellar arteries (SCAs), of which, the upper right SCA originated from PCA. We hypothesize that the poor development of the right half of the vertebrobasilar system caused the persistence of FPCA with anomalous origin of the right upper SCA as well as partial duplication of P1 segment of PCA as a remnant of the weak anastomosis between the embryonic right PCA and the basilar system. Such complex variations provide a huge challenge in their diagnosis and in choosing the suitable treatment modality for the stroke.

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来源期刊
Anatomy & Cell Biology
Anatomy & Cell Biology ANATOMY & MORPHOLOGY-
CiteScore
1.80
自引率
9.10%
发文量
75
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