Literature DB >> 18329557

Bilateral internal carotid absence: a case report of a rare congenital anomaly.

Luis F Gonzalez-Cuyar1, Dora Lam-Himlin, Fabio Tavora, Allen Burke, Rudy J Castellani.   

Abstract

BACKGROUND: Bilateral internal carotid artery agenesis (ICAA) is a rare developmental anomaly of unknown etiology that is often associated with disruption of adequate perfusion to the central nervous system. Nevertheless, some patients remain asymptomatic due to collateral circulation involving the communicating arteries of the Circle of Willis. Secondary to the hemodynamical stress through the collateral circulation, affected patients are at an increased risk of developing subarachnoid hemorrhage and intracranial aneurysms. METHODS AND
RESULTS: We report an unusual case of a 62-year-old man with bilateral ICAA who expired following two asystolic events during minor surgery.
CONCLUSION: This case emphasizes the plasticity of the cerebral collateral circulation during development, to the point of normal cerebral perfusion throughout life with no ischemic complications.

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Year:  2007        PMID: 18329557     DOI: 10.1016/j.carpath.2007.04.009

Source DB:  PubMed          Journal:  Cardiovasc Pathol        ISSN: 1054-8807            Impact factor:   2.185


  2 in total

Review 1.  Congenital absence of the bilateral internal carotid artery: a review of the associated (ab)normalities from a newborn status to the eighth decade of life.

Authors:  Ljiljana Vasović; Milena Trandafilović; Slobodan Vlajković; Goran Radenković
Journal:  Childs Nerv Syst       Date:  2017-10-23       Impact factor: 1.475

2.  Congenital absence of the internal carotid artery with a persistent primitive trigeminal artery as a collateral pathway: a report of an anatomic variation.

Authors:  Dasom Kim; Jin Wook Baek; Young Jin Heo; Hae Woong Jeong
Journal:  Surg Radiol Anat       Date:  2018-04-17       Impact factor: 1.246

  2 in total

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