Osteosarcoma is the most frequent primary cancer of the bones, and a combination of primary chemotherapy, surgery, and adjuvant chemotherapy is its current treatment. In adults, some authors have reported problems with memory and concentration following chemotherapy, but in children, severe neurologic dysfunction has been rarely reported. This report describes a 13-year-old patient with primary high-grade nonmetastatic osteosarcoma of the tibia who developed encephalopathy with super-refractory status epilepticus related to chemotherapy. He received methotrexate (MTX) and cisplatin (CDDP)-containing polychemotherapy, and after the first course of drug administration, he developed fever, confusion, a state of psychomotor agitation, and super-refractory status epilepticus with normal laboratory and imaging findings. The causal relationship between the administration of the first polychemotherapy course and his neurological manifestations may be supported by the evaluation and exclusion of other causes. The administration of antiepileptic drugs and off-label atypical antipsychotics was necessary to treat his neurological complications and behavioral changes. This patient represents the first known example of super-refractory status epilepticus in a child treated with MTX and CDDP-containing chemotherapy. Physicians should be aware that encephalopathy and seizures are possible consequences of CDDP therapy when administered alone or in combination with other chemotherapeutic agents. Further studies are needed to better define this relationship in children.

Chemotherapy-related encephalopathy with super-refractory status epilepticus in a child with osteosarcoma: A case report with a review of literature / Genova, L. D.; Perruccio, K.; Celani, M. G.; Mastrodicasa, E.; Cantisani, T. A.; Esposito, S.; Caniglia, M.. - In: FRONTIERS IN PHARMACOLOGY. - ISSN 1663-9812. - 10:(2019), p. 963. [10.3389/fphar.2019.00963]

Chemotherapy-related encephalopathy with super-refractory status epilepticus in a child with osteosarcoma: A case report with a review of literature

Esposito S.
;
2019-01-01

Abstract

Osteosarcoma is the most frequent primary cancer of the bones, and a combination of primary chemotherapy, surgery, and adjuvant chemotherapy is its current treatment. In adults, some authors have reported problems with memory and concentration following chemotherapy, but in children, severe neurologic dysfunction has been rarely reported. This report describes a 13-year-old patient with primary high-grade nonmetastatic osteosarcoma of the tibia who developed encephalopathy with super-refractory status epilepticus related to chemotherapy. He received methotrexate (MTX) and cisplatin (CDDP)-containing polychemotherapy, and after the first course of drug administration, he developed fever, confusion, a state of psychomotor agitation, and super-refractory status epilepticus with normal laboratory and imaging findings. The causal relationship between the administration of the first polychemotherapy course and his neurological manifestations may be supported by the evaluation and exclusion of other causes. The administration of antiepileptic drugs and off-label atypical antipsychotics was necessary to treat his neurological complications and behavioral changes. This patient represents the first known example of super-refractory status epilepticus in a child treated with MTX and CDDP-containing chemotherapy. Physicians should be aware that encephalopathy and seizures are possible consequences of CDDP therapy when administered alone or in combination with other chemotherapeutic agents. Further studies are needed to better define this relationship in children.
2019
Chemotherapy-related encephalopathy with super-refractory status epilepticus in a child with osteosarcoma: A case report with a review of literature / Genova, L. D.; Perruccio, K.; Celani, M. G.; Mastrodicasa, E.; Cantisani, T. A.; Esposito, S.; Caniglia, M.. - In: FRONTIERS IN PHARMACOLOGY. - ISSN 1663-9812. - 10:(2019), p. 963. [10.3389/fphar.2019.00963]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2869018
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