Meder J F, Blustajn J, Trystram D, Godon-Hardy S, Devaux B, Zuber M, Frédy D
Neuroradiology Department, Centre Hospitalier Sainte-Anne, Paris, France.
Surg Radiol Anat. 1997;19(6):385-94. doi: 10.1007/BF01628506.
We report six cases of segmental agenesis of the internal carotid a. discovered in adult patients: one case of cervical segmental agenesis (no. 1), one case of cervical and petrosal segmental agenesis (no. 2), two cases of vertical cavernous segmental agenesis (nos. 3 and 4) and two cases of distal segmental agenesis, one unilateral (no. 5) and the other bilateral (no. 6). The collateral pathways observed were: the ascending pharyngeal a. which constitutes an "intratympanic course" of the internal carotid a. (no. 1), an intercarotid anastomosis (no. 2), an arterial network at the base of the skull, the so-called "rete mirabile" (nos. 3 and 4) and the posterior communicating a. (nos. 5 and 6). Recognition of these rare dysgenesis relies upon the following radio-anatomic characteristics: reduced caliber of the a., inconsistent sparing of the carotid body, reduced diameter or even absence of the carotid canal and above all, the presence of collateral pathways. The collateral pathways allow an understanding of the segmental nature of carotid a. development and a distinction between congenital and acquired stenoses.
我们报告了在成年患者中发现的6例颈内动脉节段性发育不全病例:1例为颈部节段性发育不全(病例1),1例为颈部和岩骨段节段性发育不全(病例2),2例为海绵窦垂直段节段性发育不全(病例3和4),2例为远端节段性发育不全,其中1例为单侧(病例5),另1例为双侧(病例6)。观察到的侧支循环途径有:咽升动脉,它构成了颈内动脉的“鼓室内行程”(病例1),颈内动脉间吻合(病例2),颅底动脉网,即所谓的“神奇网”(病例3和4),以及后交通动脉(病例5和6)。对这些罕见发育异常的识别依赖于以下放射解剖学特征:动脉管径变细,颈动脉体未出现一致的保留,颈动脉管直径减小甚至缺失,最重要的是存在侧支循环途径。侧支循环途径有助于理解颈内动脉发育的节段性本质,并区分先天性和后天性狭窄。