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Pediatric Post-Pump Chorea: Case Report and Implications for Differential Diagnosis
Elisa Rossi1, Concetta Strano1, Ilaria Cortesia1
1Department of Pediatrics, University of Turin, 10126 Turin, Italy.
Insights
A child developed chorea after heart surgery, diagnosed as post-pump chorea. This rare condition highlights the need for careful diagnosis in pediatric patients experiencing movement disorders post-cardiac procedures.
Area of Science:
- Neurology
- Pediatric Cardiology
- Neuroscience
Background:
- Chorea is a neurological disorder causing involuntary movements.
- Sydenham's chorea (SC) is common in children post-streptococcal infection.
- Other conditions like autoimmune and metabolic disorders can also cause chorea.
Observation:
- A 6-year-old girl presented with chorea after mitral insufficiency surgery.
- Symptoms included weakness, slow speech, dysarthria, and sialorrhea.
- Brain imaging showed a microembolic event; other tests were negative.
Findings:
- The diagnosis of post-pump chorea was established.
- This highlights a rare complication of pediatric cardiac surgery.
- The patient recovered well with symptomatic treatment.
Implications:
- Emphasizes the importance of considering post-pump chorea in pediatric cardiac surgery patients.
- Underscores the need for a comprehensive differential diagnosis for pediatric chorea.
- Suggests potential for good recovery with appropriate management.
Background:
Chorea is a neurological disorder characterized by random, fluid movements that may affect the limbs, trunk, neck, or face. In children, Sydenham's chorea (SC) is the most common cause of acute chorea, mainly following group A beta-hemolytic streptococcal (GABHS) infection. Other autoimmune and metabolic disorders may also cause chorea.
Case Presentation:
We report the case of a 6-year-old girl who developed chorea following cardiac surgery for mitral insufficiency. One week after discharge, the patient presented with right-sided hyposthenia, slower speech, mild dysarthria, and sialorrhea. Brain MRI and intracranial MRI angiography revealed a small vascular lesion consistent with a microembolic event. Extensive diagnostic investigations, including serum panels for autoimmune encephalitis, neurotropic viruses, and metabolic disorders, were negative.
Conclusions:
Considering the patient's history, clinical course, and the exclusion of other potential causes, a diagnosis of post-pump chorea was made. This case underlines the importance of a thorough differential diagnosis in pediatric chorea and highlights post-pump chorea as a significant postoperative complication in pediatric cardiac surgery. The patient's motor symptoms improved with symptomatic treatment, and follow-up showed good recovery without neurological sequelae.
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