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A rare case of persistent hypoglossal artery associated with contralateral proximal subclavian stenosis
- Source :
- Open Medicine, Open Medicine, Vol 11, Iss 1, Pp 252-255 (2016)
- Publication Year :
- 2016
-
Abstract
- The persistent hypoglossal artery is rare vascular anomalies. We report the case of a 50-year old man with right hypoglossal artery, ipsilateral hypoplasic internal carotid artery, associated with left proximal subclavian stenosis with subclavian steal syndrome. Power-Doppler-Ultra-Sonography spectral images obtained after the patient exercised the left arm showed mid-systolic deceleration with retrograde late-systolic velocities. A Computed Tomography Angiography demonstrated a proximal stenosis of the left SA, a mild right ICA hypoplasia and an anomalous artery arising from right ICA at C2–C3 level, entering the cranium via the hypoglossal canal and joining the basilar artery. Usually the presence of PHA may be completely asymptomatic, and detected as an incidental finding by CTA or MRA, but in our case its diagnosis is extremely important because it is often the only vessel supplying blood to the basilar trunk and posterior circulation.
- Subjects :
- Arterie
Hypoglossal canal
030218 nuclear medicine & medical imaging
Persistent primitive hypoglossal artery
03 medical and health sciences
0302 clinical medicine
Abnormalitie
Arteries, Abnormalities, Persistent primitive hypoglossal artery, CT angiography
medicine.artery
Basilar artery
Medicine
Computed tomography angiography
medicine.diagnostic_test
business.industry
Medicine (all)
Arteries
General Medicine
Anatomy
medicine.disease
Hypoplasia
Stenosis
medicine.anatomical_structure
CT angiography
Special Issue on Italian Society for the Study of Vascular Anomalies
cardiovascular system
Abnormalities
Internal carotid artery
business
Subclavian steal syndrome
030217 neurology & neurosurgery
Artery
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Open Medicine, Open Medicine, Vol 11, Iss 1, Pp 252-255 (2016)
- Accession number :
- edsair.doi.dedup.....9ac3a4f908d0528711171cf7ba9bef79