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双侧颈内动脉发育不全。

Bilateral hypoplasia of the internal carotid artery.

作者信息

Bhat Dhananjaya I, Somanna Sampath, Kovoor Jerry Me

机构信息

Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.

出版信息

Indian J Radiol Imaging. 2011 Oct;21(4):257-60. doi: 10.4103/0971-3026.90682.

DOI:10.4103/0971-3026.90682
PMID:22223934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3249937/
Abstract

Agenesis and hypoplasia of the internal carotid artery (ICA) are rare congenital anomalies, occurring in less than 0.01% of the population. We report a rare case of bilateral hypoplasia of the ICA in a patient with post-traumatic subarachnoid hemorrhage. We describe the embryological development of the cerebral vasculature and present a review of literature.

摘要

颈内动脉（ICA）发育不全和发育不良是罕见的先天性异常，在人群中的发生率低于0.01%。我们报告1例创伤后蛛网膜下腔出血患者双侧ICA发育不良的罕见病例。我们描述了脑血管的胚胎发育并对文献进行综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/9be99e8cdc90/IJRI-21-257-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/5cfa651f8f60/IJRI-21-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/c6d563fe28cc/IJRI-21-257-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/3a5fa2555aaa/IJRI-21-257-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/c137312c5da3/IJRI-21-257-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/54b93e316e3d/IJRI-21-257-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/9be99e8cdc90/IJRI-21-257-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/5cfa651f8f60/IJRI-21-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/c6d563fe28cc/IJRI-21-257-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/3a5fa2555aaa/IJRI-21-257-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/c137312c5da3/IJRI-21-257-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/54b93e316e3d/IJRI-21-257-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2d/3249937/9be99e8cdc90/IJRI-21-257-g006.jpg

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Turk Neurosurg. 2009 Apr;19(2):168-71.
2
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3
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