The present paper reports a case of a 14-year-old-female adolescent who presented a single episode of syncope, without any other symptom. Axial and coronal T2-weighted magnetic resonance imaging demonstrated an absent right internal carotid artery flow void. A subsequent magnetic resonance angiography utilizing the time-of-flight technique showed absence of the right internal carotid artery. This finding was confirmed by magnetic resonance angiography of the cervical vessels, and axial computed tomography angiography showed agenesis of the right carotid canal. The literature reports such finding in association with other anomalies such as transsphenoidal encephaloceles and circle of Willis aneurysms. These associations were not observed in the present case. The patient remained asymptomatic.

Keywords: Internal carotid artery, Agenesis, Syncope

Unlike supraclinoid aneurysms, true aneurysms of the extracranial internal carotid artery are extremely rare (less than 4% of the peripheral aneurysms). The commonest presentation is a pulsatile neck swelling below the angle of the jaw associated with hoarseness, dysphagia and pain (neural compression). Concomitance with other peripherical aneurysms is frequent and caused by atherosclerosis. The morphological and hemodynamic features are very well evaluated by Doppler ultrasound, when the acoustic window is satisfactory. Identification and evaluation of these aneurysms are very important to prevent thrombosis, rupture, dissections, massive strokes and embolic brain infarcts, besides helping in the decision of the best treatment.

Keywords: Aneurysm, Extracranial internal carotid artery, Ultrasound, Doppler ultrasound, Color duplex Doppler ultrasound

Aberrant internal carotid artery is an anomaly of the embryogenesis of the vertical portion of the internal carotid artery, characterized by projection of the internal carotid artery into the middle ear, adjacent to the cochlear promontory. The authors report a case of a patient in which contrast-enhanced computed tomography and magnetic resonance angiography examinations were decisive to adequately characterize the anomaly, thus avoiding instrumental or surgical intervention, which could bear fatal consequences.

Keywords: Vascular malformation, Internal carotid artery, Congenital anomalies, Temporal bone

Heterotaxy syndrome is defined as an abnormal arrangement of some organs and vessels in association with dysmorphism. The authors describe the case of a patient with heterotaxy syndrome with poliesplenia incidentally diagnosed during imaging evaluation (computed tomography and small bowel barium study) of unrelated pathological condition.

Keywords: Heterotaxy syndrome; Polysplenia; Disorders of intestinal rotation; Partial inferior vena cava agenesis; Dorsal pancreas agenesis.