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Anteromesial Temporal Lobectomy for Medically Intractable Temporal Lobe Epilepsy: An Operative Study
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Mesial temporal sclerosis after posterior reversible encephalopathy syndrome
Mariam S Aboian1, Mithri R Junna, Karl N Krecke
1Mayo Medical School, Rochester, Minnesota, USA.
Pediatric Neurology
|August 12, 2009
Summary
Intrathecal methotrexate and posterior reversible encephalopathy syndrome can lead to mesial temporal sclerosis. This case highlights a rare progression to intractable epilepsy in a child treated for Burkitt lymphoma.
Area of Science:
- Neurology
- Oncology
- Pediatrics
Background:
- Mesial temporal sclerosis (MTS) is a common cause of epilepsy, typically associated with specific risk factors.
- Intrathecal methotrexate (IT-MTX) is a chemotherapy agent used for central nervous system malignancies.
- Posterior reversible encephalopathy syndrome (PRES) is a neurological disorder characterized by transient neurological dysfunction.
Observation:
- A pediatric patient with Burkitt lymphoma, lacking typical MTS risk factors, developed PRES and partial complex seizures.
- The patient's symptoms emerged eight days after initiating IT-MTX therapy.
- The patient's condition progressed to intractable temporal lobe epilepsy.
Findings:
- This case presents the first reported instance of IT-MTX and PRES leading to MTS.
- The development of left MTS was confirmed in the patient.
- The patient's epilepsy became refractory to treatment.
Implications:
- This case suggests a potential neurotoxic pathway involving IT-MTX and PRES contributing to MTS.
- Further research is needed to understand the mechanisms linking these conditions.
- This finding may inform treatment strategies and monitoring for pediatric patients receiving IT-MTX.
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