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Prolonged neurologic deficits with brain MRI changes following ECT in an adolescent with a CACNA1a-related disorder; a case report.
Vithayathil, Joseph; Freeman, Colbey; Jacobwitz, Marin; Schwartz, Erin Simon; Agarwal, Sonika.
Afiliación
  • Vithayathil J; Division of Neurology, Children's Hospital of Philadelphia, 3401 Civic Center Drive, Philadelphia, PA, 19104, USA. vithayathj@chop.edu.
  • Freeman C; Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, USA.
  • Jacobwitz M; Division of Neurology, Children's Hospital of Philadelphia, 3401 Civic Center Drive, Philadelphia, PA, 19104, USA.
  • Schwartz ES; Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, USA.
  • Agarwal S; Division of Neuroradiology, Children's Hospital of Philadelphia, Philadelphia, USA.
BMC Neurol ; 22(1): 466, 2022 Dec 09.
Article en En | MEDLINE | ID: mdl-36494636
BACKGROUND: Electroconvulsive therapy is used to treat depression and schizophrenia with infrequent use in pediatric patients. We report a case of an adolescent with autism spectrum disorder and acute catatonia that presented with status epilepticus (SE) and prolonged neurologic deficits with unilateral left cerebral edema on imaging following unilateral electroconvulsive therapy (ECT) on the right side, subsequently found to have a CACNA1a pathogenic variant. This case highlights a potential adverse effect of ECT in patients with CACNA1a related disorders. CASE: The patient received unilateral ECT to the right side and subsequently had an episode of SE with right-sided hemiplegia for 72 h prior to regaining some function with persistent mild right-hand weakness that persisted for at least 1-2 weeks. A brain MRI 2 days after ECT was unremarkable, but a repeat MRI on day four of admission showed left hemisphere cortical diffusion restriction, increased perfusion and T2 prolongation suggestive of cortical edema. They had whole exome genetic testing sent after discharge that showed a known pathogenic CACNA1a variant (p.I1709T). CACNA1a encodes the P/Q type calcium channels and deleterious variants in this gene result in a channelopathy associated with a spectrum of neurodevelopmental disorders that include autism spectrum disorder, hemiplegic migraine with unilateral cerebral edema, epileptic encephalopathies, or episodic ataxia syndromes. CONCLUSION: A literature review of ECT and neurologic deficits showed that most neurologic deficits resolve within 30 min of ECT. Case reports of prolonged deficits are rare and there are no prior reports of acute MRI changes related to ECT. Thus, the acute deterioration and MRI findings in this patient are likely related to the underlying CACNA1a channelopathy disorder with ECT as a precipitating event. This case report suggests care should be taken when using ECT in patients with pathogenic variants in CACNA1a. Furthermore, it reinforces the utility and importance of expanded genetic testing in patients with neurodevelopmental disorders as findings can provide valuable information that can guide treatment decisions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Edema Encefálico / Terapia Electroconvulsiva / Canalopatías / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Humans Idioma: En Revista: BMC Neurol Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Edema Encefálico / Terapia Electroconvulsiva / Canalopatías / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Humans Idioma: En Revista: BMC Neurol Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido