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Multiple Thromboembolic Cerebral Infarctions from the Aorta in a Patient with Churg-Strauss Syndrome
1Department of Neurological Surgery, Wakayama Rosai Hospital, Wakayama, Japan.
Insights
Churg-Strauss syndrome (CSS) rarely causes ischemic stroke. This case highlights aortic thrombus embolism as a potential cause, distinct from cerebral vasculitis, in CSS patients experiencing cerebral infarction.
Area of Science:
- Neurology
- Cardiology
- Rheumatology
Background:
- Churg-Strauss syndrome (CSS), a rare eosinophilic granulomatosis with polyangiitis, can present with neurological complications.
- Ischemic stroke is an uncommon manifestation of CSS, with unclear underlying mechanisms.
- Cerebral vasculitis is a recognized cause of stroke in CSS patients.
Observation:
- A 39-year-old male with CSS experienced multiple cerebral infarctions.
- Clinical diagnosis of CSS was supported by eosinophilia, asthma, sinusitis, pulmonary infiltrates, and gastric biopsy findings.
- Cerebral angiography revealed no arterial stenosis, but transesophageal echocardiography identified an aortic wall thrombus.
Findings:
- The aortic thrombus was identified as the source of cerebral embolism.
- The patient presented with hemiparesis and visual disturbances.
- The aortic thrombus resolved spontaneously within three months.
Implications:
- This case report is the first to describe cerebral infarction due to aortogenic thromboembolism in a CSS patient.
- It suggests that embolism from the cardiovascular system, specifically the aorta, should be considered in CSS-related strokes.
- This broadens the differential diagnosis for ischemic stroke in patients with Churg-Strauss syndrome beyond cerebral vasculitis.
Background:
Ischemic stroke is a rare complication of Churg-Strauss syndrome (CSS) and its pathogenesis has not been well clarified yet. We report a case of cerebral infarction in a patient with CSS due to embolism from a thrombus on the wall of the aorta.
Case:
A 39-year-old man had multiple cerebral infarctions with symptoms of mild left hemiparesis and reduced vision. He was clinically diagnosed to have CSS based on remarkable eosinophilia, history of asthma, sinusitis, pulmonary infiltrates, and histologically proven extravascular eosinophilic infiltrates in the specimen of gastric mucosa. Cerebral angiography did not show any stenotic lesions in cerebral arteries. A thrombus was detected on the wall of the aorta by transesophageal echocardiography, which was considered as the source of embolism. The thrombus resolved on follow-up examination 3 months after the onset of the stroke.
Conclusions:
This is the first case report on cerebral infarction caused by aortogenic thromboembolism in a CSS patient. Other than cerebral vasculitis, embolism from cardiovascular system, including the wall of the aorta, is a possible cause of cerebral infarctions in a CSS patient.
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