CASE 13682 Published on 29.06.2016

Brachiocephalic artery dissection

Section

Neuroradiology

Case Type

Clinical Cases

Authors

Ayesha Z Khatib, Alexander J Powles and Chee L Gan

University Hospital of Wales,
Radiology;
Heath Park CF14 4XW Cardiff
Email: azkhatib@gmail.com
Patient

87 years, female

Categories
Area of Interest Arteries / Aorta, Vascular ; Imaging Technique CT-Angiography
Clinical History
An 87-year-old female patient presented to the Emergency Department with sudden onset dysarthria and left-sided facial droop which resolved. CT head was unremarkable. In the Transient Ischaemic Attack Clinic she revealed her right hand occasionally felt cold. BP was 117/60 in the right arm and 142/66 in the left.
Imaging Findings
The patient did not have an MRI scan of the brain.
A Doppler scan of the her neck showed bi-phasic flow in the right vertebral artery and a damped subclavian artery waveform, which can represent early evidence of subclavian steal related to a non-occlusive more proximal narrowing. The waveform of the right common carotid artery was slightly damped compared with the left but there was no evidence of significant extracranial carotid artery disease bilaterally on duplex.
A subsequent CT angiogram showed an isolated dissection of the brachiocephalic artery at the origin (Fig. 1-3). Mixed plaque in the aortic arch and mural calcification of the internal carotid arteries was noted with no associated significant stenosis.
Discussion
This case demonstrates a rare example of spontaneous isolated brachiocephalic artery dissection, an unusual but important differential diagnosis in patients presenting with stroke. Supra-aortic dissection is known to be a significant cause of ischaemic stroke in patients under the age of 50 but more commonly involves the internal carotid artery and can involve the vertebral or common carotid arteries [1].
To our knowledge, only 6 other cases of spontaneous isolated brachiocephalic artery dissection have previously been reported in the literature [1, 2-5], with 2 of these patients having underlying Ehlers-Danlos syndrome. A further 2 cases of spontaneous brachiocephalic artery dissection have been reported, but these also had common carotid extension [6, 7]. Isolated brachiocephalic artery dissection following penetrating or blunt trauma has also been reported [2, 8-13].
Little is known about the specific aetiology of spontaneous isolated brachiocephalic artery dissection. In the natural history of cervical artery dissection, if atherosclerosis is excluded, it has been reported that 58.2% are spontaneous, 41.8% are associated with trauma and 7.3% have underlying fibromuscular dysplasia, the latter being seen more in females than males [14]. In our case there was no history of trauma, atherosclerosis, hypertension or known connective tissue disorder.
Our patient had transient dysarthria associated with facial droop and her right hand felt cold intermittently. It is likely that the ischaemic symptoms were the result of emboli arising from the dissection site and the upper limb symptoms related to narrowing of the brachiocephalic artery causing haemodynamic insufficiency.
Importantly, our patient’s non-contrast CT head was unremarkable, demonstrating the need for further clinical assessment to exclude other causes of her presentation. This led to additional imaging to confirm the diagnosis, highlighting the role of Doppler sonography and CT angiography as important non-invasive tools for vascular evaluation when managing patients with symptoms of acute cerebral ischaemia.
Treatment is broadly categorised into anticoagulation and antiplatelet therapy versus surgical or endovascular repair and may include blood pressure control, depending on the individual case. In our case, the patient was treated with antiplatelets and at the time of writing had no further symptoms or follow-up imaging.
Differential Diagnosis List
Isolated spontaneous brachiocephalic artery dissection
Atherosclerosis
None
Final Diagnosis
Isolated spontaneous brachiocephalic artery dissection
Case information
URL: https://eurorad.org/case/13682
DOI: 10.1594/EURORAD/CASE.13682
ISSN: 1563-4086
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