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Published on: April 21, 2017
Acute cerebral paragonimiasis presenting as hemorrhagic stroke in a child
Zhi Chen1, Gang Zhu, Jiangkai Lin
1Department of Neurosurgery, Southwest Hospital, Third Military Medical University, Chongqing, China.
Insights
Hemorrhagic stroke in children is rarely caused by cerebral paragonimiasis. This case highlights the importance of considering this parasitic infection in endemic areas when diagnosing childhood hemorrhagic strokes.
Area of Science:
- Neurology
- Infectious Diseases
- Parasitology
Background:
- Cerebral paragonimiasis is an uncommon parasitic infection of the brain.
- Hemorrhagic stroke is a rare presentation of cerebral paragonimiasis in pediatric patients.
Observation:
- A 9-year-old boy presented with acute intracerebral hemorrhage, initially mimicking a typical stroke.
- Initial investigations, including magnetic resonance angiography, did not reveal vascular abnormalities.
- Recurrent symptoms and diagnostic workup, including MRI and serology, confirmed cerebral paragonimiasis.
Findings:
- The patient's intracerebral hemorrhage was the primary clinical manifestation of acute cerebral paragonimiasis.
- Diagnosis was established through advanced neuroimaging and enzyme-linked immunosorbent assay (ELISA).
- Successful treatment with praziquantel led to gradual recovery.
Implications:
- Cerebral paragonimiasis should be included in the differential diagnosis of hemorrhagic stroke in children, particularly in endemic regions.
- Early diagnosis and treatment are crucial for favorable outcomes in pediatric cerebral paragonimiasis.
- This case underscores the diverse neurological presentations of parasitic infections in children.
Abstract:
A hemorrhagic stroke in children is rarely secondary to cerebral paragonimiasis. We describe a 9-year-old boy in whom an intracerebral hemorrhage was the leading clinical indication of acute cerebral paragonimiasis. He was hospitalized because of a sudden onset of headache, right hemiparesis, and dysarthria. A computed tomography scan revealed an intracerebral hemorrhage in the left parietal lobe. Magnetic resonance angiography did not confirm any vascular abnormalities at the location of the hematoma. Four weeks later, he presented with right hemiparesis again, and fever. A diagnosis of cerebral paragonimiasis was based on repeated magnetic resonance imaging of the brain and an enzyme-linked immunosorbent assay for paragonimiasis. The patient gradually recovered with praziquantel treatment. Cerebral paragonimiasis should be considered in the differential diagnosis of hemorrhagic strokes in children in areas where paragonimiasis is epidemic.
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