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Published on: August 22, 2012
Clinical Features and Outcomes of Pediatric Intraspinal Paragonimiasis
Yan Jiang1, Yunying Yang2, Helin Zheng3
1Department of Neurology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Neurodevelopment and Cognitive Disorders, Chongqing, People's Republic of China.
Pediatric intraspinal paragonimiasis, a rare central nervous system infection, often presents with weakness. Most children fully recover with praziquantel treatment, making surgery unnecessary.
Area of Science:
- Neurology
- Infectious Diseases
- Parasitology
Background:
- Ectopic paragonimiasis can cause severe central nervous system infections.
- Intraspinal paragonimiasis is an uncommon but serious manifestation.
- Pediatric cases require specific diagnostic and treatment considerations.
Purpose of the Study:
- To analyze diagnostic and treatment experiences for pediatric intraspinal paragonimiasis.
- To describe clinical presentation and imaging findings.
- To evaluate treatment outcomes and surgical necessity.
Main Methods:
- Retrospective analysis of pediatric patients hospitalized between 2015-2021.
- Review of clinical symptoms, spinal MRI findings, and treatment regimens.
- Assessment of patient recovery and long-term sequelae.
Main Results:
- Nine pediatric patients were included, with a median age of 9 years.
- Common symptoms included weakness, sensory disturbances, and urinary retention.
- Thoracic spinal extradural enhancing lesions were most common; praziquantel was effective, with 7/9 patients recovering fully.
Conclusions:
- Pediatric intraspinal paragonimiasis predominantly affects the thoracic spine.
- Weakness is the most frequent symptom, alongside potential sensory and sphincter issues.
- Praziquantel monotherapy is effective, and surgical intervention is typically not required.
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