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Reversible posterior leukoencephalopathy syndrome: report of 2 simultaneous cases in children
Paolo D'Angelo1, Piero Farruggia, Antonio Lo Bello
1Oncoematologia Pediatrica, Ospedale dei Bambini G. Di Cristina, Palermo, Italy.
Insights
Reversible posterior leukoencephalopathy syndrome (RPLS), a rare chemotherapy complication, occurred in two children. Prompt treatment led to full recovery from neurological deficits, allowing chemotherapy continuation.
Area of Science:
- Neurology
- Pediatric Oncology
- Radiology
Background:
- Reversible posterior leukoencephalopathy syndrome (RPLS) is an uncommon but serious neurological complication associated with cancer chemotherapy.
- Early identification and management are crucial for patient outcomes.
Observation:
- Two pediatric cases of RPLS occurred concurrently in patients undergoing different chemotherapy regimens for hepatoblastoma and acute lymphoblastic leukemia.
- Clinical presentation included altered mental status, visual disturbances, headache, seizures, back pain, and hypertension.
- MRI revealed characteristic cortical and subcortical lesions, predominantly in the occipital and parietal lobes.
Findings:
- Both patients achieved complete recovery from neuropsychological deficits within approximately ten days.
- Treatment involved anticonvulsant and antihypertensive therapies.
- Chemotherapy was successfully resumed per protocol without further neurological sequelae.
Implications:
- This case series highlights the importance of recognizing RPLS in pediatric cancer patients receiving chemotherapy.
- Aggressive management of hypertension and seizures can lead to favorable neurological recovery.
- RPLS should be considered in the differential diagnosis of neurological symptoms during cancer treatment.
Abstract:
Reversible posterior leukoencephalopathy syndrome (RPLS) is a rare complication of cancer chemotherapy. We have recently observed two cases occurred simultaneously in children receiving different chemotherapy regimens, for hepatoblastoma and acute lymphoblastic leukaemia, respectively. Both children presented with altered mental status, severe visual disturbances, headache, seizures, backpain and hypertension. Magnetic resonance imaging showed cortical and subcortical lesions especially in the occipital and parietal regions, strongly consistent with RPLS. Both patients completely recovered from their neuropsychologic deficits in about ten days only with anticonvulsant and antihypertensive therapy, and chemotherapy regimen was promptly restarted according to the planned protocol, without any neuropsychological sequela. A mild left midriasis was the only neurologic defect that persisted in the patient with acute lymphoblastic leukemia.
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