Open Access

The hyperdense basilar artery sign: a case of locked-in syndrome

  • Lasanthi Aryasinghe1Email author,
  • Yasmin Kazim1,
  • Hamza F. Obeid2 and
  • Husnain Hashim3
International Journal of Emergency Medicine20169:12

https://doi.org/10.1186/s12245-016-0104-9

Received: 18 November 2015

Accepted: 11 February 2016

Published: 29 February 2016

Abstract

Background

Locked-in syndrome, although a notoriously famous clinical entity, the rarity of the condition coupled with the variability of clinical features on acute presentation represents a potential diagnostic pitfall for the emergency physician.

Case

A previously healthy 25-year-old female was brought to our Emergency Department after being found unresponsive. On examination, she was conscious and alert with a Glasgow Coma Score of 9; on neurological examination, the patient was quadriplegic and unable to speak but was able to move her eyes and blink. Non-contrast brain computed tomography (CT) revealed a hyperdense basilar artery, and CT cerebral angiography confirmed basilar artery thrombosis.

Conclusion

This case highlights the need for a high index of suspicion to make a diagnosis of locked-in syndrome in the Emergency Department, especially in young patients with no apparent risk factors for an ischemic stroke. The hyperdense basilar artery sign is one of the earliest signs on non-contrast CT imaging and may be the only clue to guide further management in a patient with basilar artery occlusion.

Keywords

Locked-in syndromeBasilar artery thrombosisBasilar artery occlusionPosterior circulation strokeHyperdense basilar artery sign

Case presentation

A previously healthy 25-year-old female was brought to the Emergency Department after being found frothing at the mouth, unresponsive, and stiff all over. The patient had been complaining of headache, neck and shoulder pain for 2 days prior and was prescribed ibuprofen, no other history was available.

On examination, the patient was conscious and alert but appeared extremely distressed, continuously frothing at the mouth with trismus and tongue protrusion requiring regular suctioning; however, she was able to maintain her airway and all vital signs were within normal limits. She was also tearing and groaning frequently.

On neurological examination, the patient’s initial Glasgow Coma Score was 9 (eyes - 4, verbal - 2, motor - 3), her head was lateralized to the right, she was able to move her eyes and blink to command but was unable to speak, pupils were 3 mm equal and reactive, and her right upper limb was stiff and flexed (unilateral decorticate rigidity) with no movement of her left side even to noxious stimulus. Motor exam revealed increased tone with hyperreflexia in all extremities and bilateral extensor plantar reflex (upgoing plantars).

Non-enhanced computed tomography of the brain revealed a hyperdense basilar artery (Fig. 1a, b) suggestive of basilar artery thrombosis, and CT cerebral angiography confirmed a 1-cm occlusion of the basilar artery (Fig. 2).
Fig. 1

a Non-contrast CT (axial view) showing the hyperdense basilar artery sign (arrow). b Non-contrast CT (sagittal view) with the hyperdense basilar artery seen anterior to the pons

Fig. 2

CT angiography (sagittal view) revealed a 1-cm filling defect of the basilar artery (arrow)

Our patient was deemed not a candidate for thrombolysis and was managed conservatively due to several factors including a late presentation (over 10 h from last known normal) and remained locked-in at the time of her discharge from hospital.

Background

Locked-in syndrome (LIS) is a devastating clinical condition, the rarity of the condition coupled with the variability of clinical features on acute presentation represent a potential diagnostic pitfall for the emergency physician. It typically occurs as a result of an ischemic insult to the ventral pons due to thrombosis of the basilar artery but may also be seen due to hemorrhage, vertebrobasilar dissection, tumors, central pontine myelinolysis, or even multiple sclerosis involving the ventral pons [1].

Occlusion of the basilar artery, being the main vessel of the posterior circulation may produce nonspecific symptoms ranging from headache or vertigo to isolated cranial nerve palsies, hemiplegia, locked-in syndrome, or even coma [2]. Diagnosis of LIS hinges on the clinical prerequisites of quadriplegia or quadriparesis and the inability to speak (anarthria) with preservation of consciousness and eye movements or blinking. Three categories of LIS have been described; the classic in which the patient has intact vertical eye movements, incomplete LIS which is similar to the classic with remnants of some voluntary motor control, and total LIS in which the patient is fully conscious but has complete immobility including eye movements [1].

As with any acute stroke, a non-enhanced head CT should be performed promptly; the hyperdense basilar artery sign (Fig. 1a), similar to the hyperdense middle cerebral artery sign in anterior circulation strokes, may be the only finding in an acute presentation and has been shown to be a strong predictor of basilar artery thrombosis in patients with a high pretest probability for a posterior circulation stroke (71 % sensitivity, 98 % specificity) [3, 4].

Emergency Department management of these patients involve airway and hemodynamic management, with neuromedical consultation for intravenous thrombolysis within 4.5 h of symptom onset or intra-arterial thrombolysis (IAT) within 6 h [2]; with some studies advocating the use of IAT in acute basilar artery occlusions 12 to 24 h after symptom onset [5] due to the extremely poor functional prognosis of the condition. In patients with failed recanalization after IV thrombolysis, studies have shown promising results with the use of mechanical endovascular interventions [6].

Conclusions

Awareness of the clinical features suggestive of a posterior circulation stroke and recognition of the hyperdense basilar artery sign on non-contrast CT, with rapid confirmation of the diagnosis via multimodal CT or MRI and initiation of intravenous or intra-arterial thrombolysis will decrease the high mortality and morbidity associated with this devastating condition.

Consent

Written informed consent was obtained from the patient’s next of kin for publication of this report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request.

Declarations

Funding

No funding was required in preparation of the manuscript.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors’ Affiliations

(1)
Department of Emergency Medicine, Rashid Hospital Trauma Center
(2)
Department of Internal Medicine, Rashid Hospital Trauma Center
(3)
Department of Neurology, Rashid Hospital Trauma Center

References

  1. Smith E, Delargy M. Locked-in syndrome. Br Med J. 2005;330:406–9.View ArticleGoogle Scholar
  2. Schonewille WJ, Wijman CAC, Michel P, et al. Treatment and outcomes of acute basilar artery occlusion in the Basilar Artery International Cooperation Study (BASICS): a prospective registry study. Lancet Neurol. 2009;8:724–30.View ArticlePubMedGoogle Scholar
  3. Goldmakher GV, Camargo EC, Furie KL, et al. Hyperdense basilar artery sign on unenhanced CT predicts thrombus and outcome in acute posterior circulation stroke. Stroke. 2009;40(1):134–9.View ArticlePubMedGoogle Scholar
  4. Connell L et al. Hyperdense basilar artery sign—a reliable sign of basilar artery occlusion. Neuroradiology. 2012;54:321–7.View ArticlePubMedGoogle Scholar
  5. Savitz SI, Caplan LR. Vertebrobasilar disease. N Engl J Med. 2005;352:2618.View ArticlePubMedGoogle Scholar
  6. Mattle HP et al. Basilar artery occlusion. Lancet Neurol. 2011;10:1002–14.View ArticlePubMedGoogle Scholar

Copyright

© Aryasinghe et al. 2016