Skip to main content
Top
Gepubliceerd in: Journal of Autism and Developmental Disorders 12/2019

19-02-2019 | Letter to the Editor

Recovery from Autism after Successful Surgery for a Benign Brain Tumor Associated with Epilepsy

Auteurs: Michal Hrdlicka, Martin Kudr, Pavel Krsek, Michal Tichy, Martin Kyncl, Josef Zamecnik, Marketa Mohaplova, Iva Dudova

Gepubliceerd in: Journal of Autism and Developmental Disorders | Uitgave 12/2019

Log in om toegang te krijgen
share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Excerpt

A rare example of syndromic autism is autism spectrum disorder (ASD) in children with brain tumors. The case reports on this association are few and mostly involve autism and cerebellar pilocytic astrocytoma (Omar et al. 2009; Adachi et al. 2012; Minhas et al. 2013), right temporal ganglioglioma (Mikati et al. 2009), and mesial temporal oligodendroglioma (Hoon and Reiss 1992). The majority of the described cases underwent neurosurgery for removal of the brain tumor (Adachi et al. 2012; Minhas et al. 2013; Mikati et al. 2009; Hoon and Reiss 1992). Following surgery, autism remained unchanged (Adachi et al. 2012), was minimally or mildly improved (Hoon and Reiss 1992; Mikati et al. 2009), or autism improvement was not specified (Minhas et al. 2013). …
Literatuur
go back to reference Adachi, K., Murai, Y., & Teramoto, A. (2012). Infantile cerebellar pilocytic astrocytoma with autism spectrum disorder. Journal of Nippon Medical School, 79, 228–231.CrossRef Adachi, K., Murai, Y., & Teramoto, A. (2012). Infantile cerebellar pilocytic astrocytoma with autism spectrum disorder. Journal of Nippon Medical School, 79, 228–231.CrossRef
go back to reference Amiet, C., Gourfinkel-An, I., Bouzamondo, A., Tordjman, S., Baulac, M., Lechat, P., et al. (2008). Epilepsy in autism is associated with intellectual disability and gender: Evidence from a meta-analysis. Biological Psychiatry, 64, 577–582.CrossRef Amiet, C., Gourfinkel-An, I., Bouzamondo, A., Tordjman, S., Baulac, M., Lechat, P., et al. (2008). Epilepsy in autism is associated with intellectual disability and gender: Evidence from a meta-analysis. Biological Psychiatry, 64, 577–582.CrossRef
go back to reference Baron-Cohen, S., Ring, H. A., Bullmore, E. T., Wheelwright, S., Ashwin, C., & Williams, S. C. (2000). The amygdala theory of autism. Neuroscience and Biobehavioral Reviews, 24, 355–364.CrossRef Baron-Cohen, S., Ring, H. A., Bullmore, E. T., Wheelwright, S., Ashwin, C., & Williams, S. C. (2000). The amygdala theory of autism. Neuroscience and Biobehavioral Reviews, 24, 355–364.CrossRef
go back to reference Ben-Ari, Y., & Holmes, G. L. (2006). Effects of seizures on developmental processes in the immature brain. Lancet Neurology, 5, 1055–1063.CrossRef Ben-Ari, Y., & Holmes, G. L. (2006). Effects of seizures on developmental processes in the immature brain. Lancet Neurology, 5, 1055–1063.CrossRef
go back to reference Brooks-Kayal, A. (2010). Epilepsy and autism spectrum disorders: Are there common developmental mechanisms? Brain and Development, 32, 731–738.CrossRef Brooks-Kayal, A. (2010). Epilepsy and autism spectrum disorders: Are there common developmental mechanisms? Brain and Development, 32, 731–738.CrossRef
go back to reference Christensen, D. L., Baio, J., Van Naarden Braun, K., Bilder, D., Charles, J., Constantino, J. N., et al. (2016). Prevalence and characteristics of autism spectrum disorder among children aged 8 years—Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012. Morbidity and Mortality Weekly Report Surveillance Summaries, 65(3), 1–23.PubMed Christensen, D. L., Baio, J., Van Naarden Braun, K., Bilder, D., Charles, J., Constantino, J. N., et al. (2016). Prevalence and characteristics of autism spectrum disorder among children aged 8 years—Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012. Morbidity and Mortality Weekly Report Surveillance Summaries, 65(3), 1–23.PubMed
go back to reference Flint, A. E., Waterman, M., Bowmer, G., Vadlamani, G., Chumas, P., & Morrall, M. C. H. J. (2017). Neuropsychological outcomes following paediatric temporal lobe surgery for epilepsies: Evidence from a systematic review. Seizure, 52, 89–116.CrossRef Flint, A. E., Waterman, M., Bowmer, G., Vadlamani, G., Chumas, P., & Morrall, M. C. H. J. (2017). Neuropsychological outcomes following paediatric temporal lobe surgery for epilepsies: Evidence from a systematic review. Seizure, 52, 89–116.CrossRef
go back to reference Helt, M., Kelley, E., Kinsbourne, M., Pandey, J., Boorstein, H., Herbert, M., & Fein, D. (2008). Can children with autism recover? If so, how? Neuropsychology Review, 18, 339–366.CrossRef Helt, M., Kelley, E., Kinsbourne, M., Pandey, J., Boorstein, H., Herbert, M., & Fein, D. (2008). Can children with autism recover? If so, how? Neuropsychology Review, 18, 339–366.CrossRef
go back to reference Hoon, A. H., & Reiss, A. L. (1992). The mesial-temporal lobe and autism: Case report and review. Developmental Medicine and Child Neurology, 34, 252–265.CrossRef Hoon, A. H., & Reiss, A. L. (1992). The mesial-temporal lobe and autism: Case report and review. Developmental Medicine and Child Neurology, 34, 252–265.CrossRef
go back to reference Hrdlicka, M., Komarek, V., Propper, L., Kulisek, R., Zumrova, A., Faladova, L., et al. (2004). Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism. European Child and Adolescent Psychiatry, 13, 209–213.CrossRef Hrdlicka, M., Komarek, V., Propper, L., Kulisek, R., Zumrova, A., Faladova, L., et al. (2004). Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism. European Child and Adolescent Psychiatry, 13, 209–213.CrossRef
go back to reference Lai, M. C., Lombardo, M. V., & Baron-Cohen, S. (2014). Autism. Lancet, 383, 896–910.CrossRef Lai, M. C., Lombardo, M. V., & Baron-Cohen, S. (2014). Autism. Lancet, 383, 896–910.CrossRef
go back to reference Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Leventhal, B. L., DiLavore, P. C., et al. (2000). The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205–223.CrossRef Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Leventhal, B. L., DiLavore, P. C., et al. (2000). The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205–223.CrossRef
go back to reference Lord, C., Rutter, M., & LeCouteur, A. (1994). Autism diagnostic interview—Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. Journal of Autism and Developmental Disorders, 24, 659–685.CrossRef Lord, C., Rutter, M., & LeCouteur, A. (1994). Autism diagnostic interview—Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. Journal of Autism and Developmental Disorders, 24, 659–685.CrossRef
go back to reference Mikati, M. A., El-Bitar, M. K., Najjar, M. W., Rbeiz, J. J., Barada, W. H., Najjar, V. F., et al. (2009). A child with refractory complex partial seizures, right temporal ganglioglioma, contralateral continuous electrical status epilepticus, and a secondary Landau–Kleffner autistic syndrome. Epilepsy and Behavior, 14, 411–417.CrossRef Mikati, M. A., El-Bitar, M. K., Najjar, M. W., Rbeiz, J. J., Barada, W. H., Najjar, V. F., et al. (2009). A child with refractory complex partial seizures, right temporal ganglioglioma, contralateral continuous electrical status epilepticus, and a secondary Landau–Kleffner autistic syndrome. Epilepsy and Behavior, 14, 411–417.CrossRef
go back to reference Minhas, H. M., Pescosolido, M. F., Schwede, M., Piasecka, J., Gaitanis, J., Tantravahi, U., et al. (2013). An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma. American Journal of Medical Genetics Part A, 161, 787–791.CrossRef Minhas, H. M., Pescosolido, M. F., Schwede, M., Piasecka, J., Gaitanis, J., Tantravahi, U., et al. (2013). An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma. American Journal of Medical Genetics Part A, 161, 787–791.CrossRef
go back to reference Nicolson, R., DeVito, T. J., Vidal, C. N., Sui, Y., Hayashi, K. M., Drost, D. J., et al. (2006). Detection and mapping of hippocampal abnormalities in autism. Psychiatry Research, 148, 11–21.CrossRef Nicolson, R., DeVito, T. J., Vidal, C. N., Sui, Y., Hayashi, K. M., Drost, D. J., et al. (2006). Detection and mapping of hippocampal abnormalities in autism. Psychiatry Research, 148, 11–21.CrossRef
go back to reference Omar, A. O., Ahmad, A. E., El Bashir, H., & Al Jaber, M. J. (2009). Trisomy 13 in a 7-year-old girl with cerebellar tumor, eye abnormalities, and autistic features. American Journal of Medical Genetics Part A, 149, 1056–1057.CrossRef Omar, A. O., Ahmad, A. E., El Bashir, H., & Al Jaber, M. J. (2009). Trisomy 13 in a 7-year-old girl with cerebellar tumor, eye abnormalities, and autistic features. American Journal of Medical Genetics Part A, 149, 1056–1057.CrossRef
go back to reference Shubrata, K. S., Sinha, S., Seshadri, S. P., Girimaji, S., Subbakrishna, D. K., & Srinath, S. (2015). Childhood autism spectrum disorders with and without epilepsy: Clinical implications. Journal of Child Neurology, 30, 476–482.CrossRef Shubrata, K. S., Sinha, S., Seshadri, S. P., Girimaji, S., Subbakrishna, D. K., & Srinath, S. (2015). Childhood autism spectrum disorders with and without epilepsy: Clinical implications. Journal of Child Neurology, 30, 476–482.CrossRef
go back to reference Strasser, L., Downes, M., Kung, J., Cross, J. H., & De Haan, M. (2018). Prevalence and risk factors for autism spectrum disorder in epilepsy: A systematic review and meta-analysis. Developmental Medicine and Child Neurology, 60, 19–29.CrossRef Strasser, L., Downes, M., Kung, J., Cross, J. H., & De Haan, M. (2018). Prevalence and risk factors for autism spectrum disorder in epilepsy: A systematic review and meta-analysis. Developmental Medicine and Child Neurology, 60, 19–29.CrossRef
go back to reference Viscidi, E. W., Triche, E. W., Pescosolido, M. F., McLean, R., Joseph, R. M., Spence, S. J., et al. (2013). Clinical characteristics of children with autism spectrum disorder and co-occuring epilepsy. PLoS One, 8, e67797.CrossRef Viscidi, E. W., Triche, E. W., Pescosolido, M. F., McLean, R., Joseph, R. M., Spence, S. J., et al. (2013). Clinical characteristics of children with autism spectrum disorder and co-occuring epilepsy. PLoS One, 8, e67797.CrossRef
go back to reference World Health Organization. (1992). International Classification of Diseases (10th ed.). Geneva: WHO. World Health Organization. (1992). International Classification of Diseases (10th ed.). Geneva: WHO.
Metagegevens
Titel
Recovery from Autism after Successful Surgery for a Benign Brain Tumor Associated with Epilepsy
Auteurs
Michal Hrdlicka
Martin Kudr
Pavel Krsek
Michal Tichy
Martin Kyncl
Josef Zamecnik
Marketa Mohaplova
Iva Dudova
Publicatiedatum
19-02-2019
Uitgeverij
Springer US
Gepubliceerd in
Journal of Autism and Developmental Disorders / Uitgave 12/2019
Print ISSN: 0162-3257
Elektronisch ISSN: 1573-3432
DOI
https://doi.org/10.1007/s10803-019-03935-z

Andere artikelen Uitgave 12/2019

Journal of Autism and Developmental Disorders 12/2019 Naar de uitgave