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Internal carotid artery (ICA) dissection is a rare and potentially devastating cause of cerebral ischaemia, initiated by an intimal tear or rupture of the vasa vasorum, that can lead to an intraluminal thrombus, vascular stenosis, occlusion, or dissecting aneurysm formation. Management is challenging due to its complex pathophysiology and non-specific nature of symptoms. In this case-control study, we were able to document the clinical presentation and management of an ICA dissection in a hypertensive, 50-year-old male triathlete following an acute bout of intermittent apnoeic (pyramid breathing) swimming. He developed blurred vision in his left eye, ipsilateral headache, pulsatile tinnitus and later noticed left-sided ptosis and pupil miosis consistent with Horner's syndrome, prompting specialist referral. Neuroimaging confirmed a dissection of the left ICA and incidental pseudoaneurysm of the distal right ICA. The patient recovered well due to a combination of pharmacological/dietary management of hypertension and graduated, structured return to physical activity and competition, culminating in significant re-expansion of the ICA true lumen calibre. We also conducted a laboratory-based, dry-land, static swimming simulation in an age- and physical activity-matched healthy male control. This demonstrated that exercise-induced ICA shear stress was more exaggerated during dynamic apnoeic breathing compared to normal breathing, which, in the setting of the patient's hypertension, may have been a precipitating factor underlying ICA dissection. Collectively, these findings provide unique insights into the pathophysiology and management of this rare condition while highlighting the inherent risks associated with this mode of exercise training in susceptible individuals with hypertension.
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http://dx.doi.org/10.1113/EP093047 | DOI Listing |
Vasc Endovascular Surg
September 2025
Department of Vascular and Endovascular Surgery, University Hospital Centre Bordeaux, Bordeaux, France.
Spontaneous recanalization (SR) of an internal carotid artery (ICA) is a rare phenomenon. Cases reported in literature described the evolution of dissection or atherothrombotic / cardioembolic acute occlusions. No case of post-endarterectomy ICA occlusion resolved by SR has never been reported.
View Article and Find Full Text PDFCan J Ophthalmol
August 2025
Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, ON, Canada; Division of Neurology, Department of Medicine, University of Toronto, Toronto, ON, Canada; Kensington Vision and Research Centre, Toronto, ON, Canada. Electronic address:
Objective: To determine the prevalence of structural causes in pharmacologically confirmed Horner syndrome (HS) and assess the clinical significance of incidental neuroimaging findings.
Design: A retrospective cohort study.
Participants: A total of 134 patients with pharmacologically confirmed HS who underwent neuroimaging at a tertiary neuro-ophthalmology clinic between July 2018 and June 2024.
Cureus
July 2025
Stroke Medicine, Dorset County Hospital, Dorchester, GBR.
Internal carotid artery (ICA) dissection often presents with headache and neck pain, along with symptoms related to the anterior circulation if stroke occurs. Less commonly, it may cause Horner's syndrome and involvement of the lower cranial nerves (IX, X, XI, and XII). However, it is rare for ICA dissection to present with pulsatile tinnitus and hearing loss, which is typically linked to vertebral artery dissection.
View Article and Find Full Text PDFRadiol Case Rep
November 2025
Riverside Community Hospital, 4445 Magnolia Avenue, Riverside, CA, USA.
Internal carotid artery dissection and pseudoaneurysm is a rare vascular abnormality that can result in a wide range of morbidity and mortality. There is a variety of treatment options that are often dependent on the degree of presenting symptoms. The case presented herein is that of a 43-year-old man that is otherwise healthy presenting with cranial neuropathy related to a left internal carotid artery pseudoaneurysm.
View Article and Find Full Text PDFJ Vet Intern Med
August 2025
Anicura "Ospedale Veterinario I Portoni Rossi", Zola Predosa, Bologna, Italy.
A 5-year-old male golden retriever was presented after a subacute onset of left-sided Horner syndrome (HS). The dog had anisocoria with left-sided miosis, ptosis of the upper eyelid, and third eyelid protrusion in the left eye. Because of the absence of additional neurological abnormalities, clinical signs were suggestive of left isolated HS, and the lesion was localized at the level of either the preganglionic or postganglionic neuron of the sympathetic chain.
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