Tubbs R Shane, Oakes W Jerry
Department of Cell Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Childs Nerv Syst. 2005 Jan;21(1):81-2. doi: 10.1007/s00381-003-0893-z. Epub 2004 Jan 23.
Only two previous reports of agenesis of the internal carotid artery with a coexistent Horner's syndrome are to be found in the medical literature.
We report a case of a male child seen initially for what was presumed to be a traumatic superficial temporal artery aneurysm. MRA incidentally revealed ipsilateral agenesis of the internal carotid artery. This child's physical exam included ipsilateral Horner's syndrome.
This case report illustrates that agenesis of the internal carotid artery does indeed cause Horner's syndrome in some cases. The clinician who diagnoses a patient with Horner's syndrome should remember that agenesis of the internal carotid artery may be the cause as this entity can be associated in itself with other pathologies of the central nervous system.
医学文献中仅能找到两篇关于颈内动脉发育不全并存霍纳综合征的报告。
我们报告一例男童,最初因疑似创伤性颞浅动脉瘤前来就诊。磁共振血管造影偶然发现同侧颈内动脉发育不全。该患儿的体格检查包括同侧霍纳综合征。
本病例报告表明,颈内动脉发育不全在某些情况下确实会导致霍纳综合征。诊断为霍纳综合征的临床医生应记住,颈内动脉发育不全可能是病因,因为该病症本身可能与中枢神经系统的其他病变有关。