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Posterior reversible encephalopathy syndrome in childhood with hematologic/oncologic diseases
Sung Chul Won1, Seung Yeon Kwon, Jung Woo Han
1Department of Pediatrics, College of Medicine, Yonsei University, Seoul, Korea.
Insights
Posterior reversible encephalopathy syndrome (PRES) is a rare neurological complication in pediatric cancer patients. This study suggests chemotherapy and surgery may also contribute to PRES, alongside immunosuppressive agents.
Area of Science:
- Neurology
- Pediatric Oncology
- Radiology
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological condition characterized by specific MRI findings and clinical symptoms.
- It is a rare central nervous system complication in childhood hematologic-oncologic patients, with varied neurological presentations.
- The exact causes of PRES are not fully understood.
Purpose of the Study:
- To review cases of PRES in pediatric patients with hematologic-oncologic conditions.
- To identify potential contributing factors to PRES beyond known causes.
- To highlight the importance of recognizing this complication for timely management.
Main Methods:
- Retrospective review of 8 pediatric patients diagnosed with PRES.
- Analysis of patient diagnoses, treatments (chemotherapy, immunosuppressants, stem cell transplantation), and surgical history.
- Correlation of clinical symptoms and characteristic MRI findings.
Main Results:
- The study included patients with acute lymphocytic leukemia, aplastic anemia, and solid tumors.
- All patients experienced seizures and presented with typical PRES MRI findings.
- Follow-up MRIs showed significant improvement in all patients.
Conclusions:
- Chemotherapy and surgery may be additional contributing factors to PRES in pediatric oncology patients, besides immunosuppressive agents.
- Close monitoring of patients undergoing chemotherapy and surgery is crucial for early detection of PRES.
- PRES, though uncommon, appears to have a good prognosis with appropriate management.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is a clinico-neuroradiologic disease entity represented by characteristic magnetic resonance image (MRI) findings of subcortical/cortical hyperintensity in T2-weighted sequences, more often observed in parieto-occipital lobes, accompanied by clinical neurologic alterations. PRES is a rare central nervous system complication in childhood hematologic-oncologic patients and shows very different neurologic symptoms between patients, from numbness on extremities to generalized seizure. The etiology of PRES was not well known until these days. In this study, 8 patients with PRES were reviewed, retrospectively. There were 4 patients with acute lymphocytic leukemia, 1 with aplastic anemia, and 3 with solid tumors (1 patient each for neuroblastoma, Ewing sarcoma, and osteosarcoma). Allogeneic stem cell transplantation was performed in 2 patients. Immunosuppressive agents such as tacrolimus and cyclosporine A were used in 3 patients. One neuroblastoma patient was in immediate postoperative status. All patients experienced seizure attacks of different types and showed typical MRI findings. Follow-up MRIs revealed significant improvements. From this review, we might consider chemotherapy and surgery as additive causes for PRES other than immunosuppressive agents. Therefore, careful examination of the patients receiving chemotherapy and surgery was needed to find out this uncommon but good prognostic complication.
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