A 31-year-old man with no prior medical history presented to the emergency department with sudden-onset right-sided limb numbness and weakness accompanied by severe neck pain after prolonged rope skipping. He denied any history of trauma, neck manipulation or recent infections. He was a nonsmoker, did not consume alcohol and denied drug use. On admission, his blood pressure was 200/110 mmHg. Neurological examination revealed right-sided Horner’s syndrome, ipsilateral reduced superficial sensation, C2 anesthesia, muscle weakness (grade 3/5), proprioceptive impairment and hyperpathia affecting the trunk and limbs. The deep tendon reflexes were hypoactive on the right side, and Babinski’s sign was negative. The patient did not report urinary retention or constipation.
Acute ischemic stroke was suspected, and a non-contrast CT scan of the head was unremarkable. All hematological examinations were also unremarkable. CT angiography of the head and cervical region revealed diffuse thinning of the right vertebral artery. A brain MRI demonstrated abnormal diffusion-weighted imaging and T2-weighted imaging hyperintensity in the right posterolateral lower medulla oblongata, indicative of spinal cord infarction (SCI) in the posterior spinal artery (PSA) territory. A cervical spine MRI confirmed infarction extending from the right lower medulla oblongata to the upper cervical spinal cord at the C2 level (Figure 1A), supporting the diagnosis of unilateral posterior spinal artery syndrome (PSAS). High-resolution MRI further identified an intramural hematoma in the right vertebral artery at the V3 segment (Figure 1B), consistent with vertebral artery dissection (VAD). Following antiplatelet therapy and rehabilitation, the patient demonstrated significant neurological improvement.

Figure 1. (A) T2-weighted and diffusion-weighted magnetic resonance imaging (MRI) showed long segment hyperintense signal lesions from the right lower medulla oblongata to the upper cervical spinal cord at the C2 level (red arrow). (B) High-resolution MRI showed intramural hematoma in the right vertebral artery at V3 segment, indicative of vertebral artery dissection (VAD) (yellow arrowhead).
PSAS is a rare form of SCI, with an incidence significantly lower than that of cerebral ischemic stroke. Reference Panesar, Conry, Finocchi, Desai and Bracewell1,Reference Jiang, Tian and Jing2 It was first described in 1895 when Williamson identified ischemia in the PSA territory as a cause of myelopathy. Reference W.3 Clinically, PSAS is characterized by limb paralysis, impairment of superficial and proprioceptive sensation and potential urinary or bowel dysfunction, with MRI findings typically revealing lesions in the dorsal columns, dorsal horns and posterior spinal cord. Reference Chen, Liu and Qiu4
Upper cervical PSAS is particularly uncommon, with only 23 cases reported over the past 40 years, including the present case. The primary etiologies of upper cervical PSAS include VAD, atherosclerosis, iatrogenic causes and trauma. Reference Chen, Liu and Qiu4,Reference Matsubayashi, Tsuchiya and Shimizu5 Among the 23 cases, VAD accounted for 13 patients, with a median age of 34.5 years (Supplementary table). Unlike atherosclerosis, which is more common in the elderly, VAD is a leading cause of PSAS in younger individuals. Reference Jiang, Tian and Jing2,Reference Ouyang, Li, Zeng, Wang and Fan6 VAD itself is an uncommon etiology of ischemic stroke and can be triggered by high-impact trauma to the head or neck or by extreme neck movements, such as hyperextension or rotation. Reference Saw, McIntosh, Kountouris, Newman and Gaida7–Reference Pryse-Phillips9 High-intensity sports are a recognized risk factor for VAD, particularly in young adults. Reference Toluie, Joseph and Hrehorovich10
This case provides representative neuroimaging findings of a rare condition, contributing to educational purpose. Furthermore, in young patients without conventional risk factors who present with acute ischemic stroke symptoms, particularly when accompanied by severe neck pain, arterial dissection should be considered as a potential cause. For patients diagnosed with PSAS, high-resolution MRI is essential to identify the underlying pathology and guide appropriate management.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/cjn.2025.47.
Author contributions
Di Wu performed a literature review, collate the information of the patient and drafted the manuscript; Qian Sun cared for the patient, collate the neuroimages of the patient and critically reviewed the manuscript; Jing Zhao cared for the patient and critically revised the manuscript; and Lan Zheng conceptualized and supervised the work, cared for the patient and critically revised the manuscript.
Funding statement
This research was funded by the grant number 2022MHPY02 from Minhang Hospital, Fudan University.
Competing interests
The authors do not have any conflicts of interest to disclose.
Ethical statement
This study was approved by the Ethical Review Board of Minhang Hospital of Fudan University.
Statements and declarations
The manuscript has not been published elsewhere and is not under consideration by any other journal. All authors have approved the manuscript.