Congenital absence or hypoplasia of the carotid artery: Radioclinical issues

• Published in: American journal of otolaryngology 2004-09, Vol.25 (5), p.339-349
• Main Authors: TASAR, Mustafa, YETISER, Sertac, TASAR, Aysin, UGUREL, Sahin, GÖNÜL, Engin, SAGLAM, Mutlu
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Angiography; Biological and medical sciences; Carotid Arteries - abnormalities; Carotid Arteries - diagnostic imaging; Female; Humans; Magnetic Resonance Imaging; Male; Medical sciences; Middle Aged; Otorhinolaryngology. Stomatology; Retrospective Studies; Tomography, X-Ray Computed; Ultrasonography, Doppler, Transcranial
• ISSN: 0196-0709; 1532-818X
• DOI: 10.1016/j.amjoto.2004.04.008

Congenital anomaly of the carotid artery is a rare abnormality. It is usually discovered incidentally by color Doppler carotid sonography, angiography, computed tomography (CT), or magnetic resonance imaging (MRI) of the head and neck taken for some other reason. Most patients are not symptomatic because of sufficient cerebral circulation supplied to the defective area by the communicating arteries of the circle of Willis, intercavernous anastomosis, communicating arteries from external carotid artery, and by persistent embryologic arteries to the carotid artery territory. However, sometimes, this anatomic variation may eventually lead to some clinical signs and symptoms in particular circumstances in the head and neck of which surgeons are unaware. A retrospective study was designed to emphasize the characteristic radiologic and clinical picture in patients with the congenital absence (agenesis and aplasia) or hypoplasia of the carotid artery, to delineate the associated abnormalities and existing collateral vessels, and to find out its incidence. Five thousand one hundred cerebral MRI and/or catheter angiograms performed between February 1988 and March 2002 were reviewed for carotid artery abnormality. Seven patients with congenital absence or hypoplasia (4 of these patients were presented with hypoplasia of internal carotid artery [ICA], 3 with absence of ICA) of ICA were identified (0.13%). The radiologic and clinical study of 5 patients with unilateral (3 of these patients were presented with hypoplasia and 2 with absence of ICA) and 2 patients with bilateral (1 was presented with absence of ICA, whereas the other was hypoplasia) congenital abnormality with absence or hypoplasia of ICA demonstrate that those patients are usually asymptomatic and they are diagnosed incidentally. It has been concluded that the combined use of magnetic resonance angiography and CT scanning of the skull base may disclose small but patent ICA. Collateral vessels seem to be usual in such cases, but they may be prominent in cases of acquired vascular occlusion, or increased hemodynamic pressure in dysplastic changes in collateral arteries are known causes of aneurysms. The main vascular supply for the brain in patients with congenitally small (hypoplasia) or absent (agenesis or aplasia) ICA is the vertebrobasilar system in bilateral cases. However, contralateral carotid vessel is the dominant arterial supply for unilateral cases, which has to be borne in mind in surgical int