The natural history of epilepsy and nonepileptic seizures in Sturge-Weber syndrome: A retrospective case-note review

被引:1
作者
Male, Rhian [1 ]
Eriksson, Sofia H. [1 ,2 ]
机构
[1] UCL, Inst Neurol, Dept Clin & Expt Epilepsy, London, England
[2] UCL, Natl Hosp Neurol & Neurosurg, Inst Neurol, Dept Clin & Expt Epilepsy, Box 29, London WC1N 3BG, England
关键词
Epilepsy; Sturge-Weber syndrome; Nonepileptic seizures; Natural history; Prognosis; Seizures; ONSET; MULTICENTER; SURGERY;
D O I
10.1016/j.yebeh.2023.109303
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Objective: Patients with Sturge-Weber Syndrome (SWS) experience varying degrees of neurological problems - including epilepsy, hemiparesis, learning disability (LD), and stroke-like episodes. While the range of clinical problems experienced by children with SWS is well recognized, the spectrum of clinical presentation and its treatment during adulthood has been relatively neglected in the literature to date. This study explored the natural history of epileptic and nonepileptic seizures into adulthood in patients with SWS, and their treatment, and investigated whether any clinical factors predict which symptoms a patient will experience during adulthood.Methods: A retrospective case-note review of a cohort of 26 adults with SWS at the National Hospital for Neurology and Neurosurgery (NHNN). Childhood data were also recorded, where available, to enable review of change/development of symptoms over time.Results: The course of epilepsy showed some improvement in adulthood - seventeen adults continued to have seizures, while six patients gained seizure freedom, and no one had adult-onset seizures. However, seizures did worsen for some patients. Although no factors reached statistical significance regarding predicting continued epilepsy in adulthood, being male, more severe LD, having required epilepsy surgery, and bilateral cortical involvement may be important. Nonepileptic seizures (NES) also began during adulthood for four patients.Significance: By adulthood, there is some degree of improvement in epilepsy overall; while NES may occur for the first time. While the majority of the results did not survive adjustments for multiple comparisons, some interesting trends appeared, which require further investigation in a multicenter national audit. Patients with more neurologically severe presentations during childhood may continue to experience seizures. Careful monitoring and screening are needed during adulthood, to detect changes and newly developing symptoms such as NES, and target treatment promptly.& COPY; 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页数:9
相关论文
共 38 条
  • [1] Clinical Outcomes in Bilateral Sturge-Weber Syndrome
    Alkonyi, Balint
    Chugani, Harry T.
    Karia, Samir
    Behen, Michael E.
    Juhasz, Csaba
    [J]. PEDIATRIC NEUROLOGY, 2011, 44 (06) : 443 - 449
  • [2] Sturge-Weber syndrome - Indications and results of surgery in 20 patients
    Arzimanoglou, AA
    Andermann, F
    Aicardi, J
    Sainte-Rose, C
    Beaulieu, MA
    Villemure, JG
    Olivier, A
    Rasmussen, T
    [J]. NEUROLOGY, 2000, 55 (10) : 1472 - 1479
  • [3] Epidemiology of psychogenic nonepileptic seizures
    Asadi-Pooya, Ali A.
    Sperling, Michael R.
    [J]. EPILEPSY & BEHAVIOR, 2015, 46 : 60 - 65
  • [4] Sturge-Weber Syndrome
    Bachur, Catherine D.
    Comi, Anne M.
    [J]. CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2013, 15 (05) : 607 - 617
  • [5] Factors affecting seizure outcome after epilepsy surgery: an observational series
    Bell, Gail S.
    de Tisi, Jane
    Gonzalez-Fraile, Juan Carlos
    Peacock, Janet L.
    McEvoy, Andrew W.
    Harkness, William F. J.
    Foong, Jacqueline
    Pope, Rebecca A.
    Diehl, Beate
    Sander, Josemir W.
    Duncan, John S.
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2017, 88 (11) : 933 - 940
  • [6] Comi Anne M, 2015, Handb Clin Neurol, V132, P157, DOI 10.1016/B978-0-444-62702-5.00011-1
  • [7] Comi Anne M, 2007, Expert Rev Neurother, V7, P951, DOI 10.1586/14737175.7.8.951
  • [8] A Multidisciplinary Consensus for Clinical Care and Research Needs for Sturge-Weber Syndrome
    De la Torre, Alejandro J.
    Luat, Aimee F.
    Juhasz, Csaba
    Ho, Mai Lan
    Argersinger, Davis P.
    Cavuoto, Kara M.
    Enriquez-Algeciras, Mabel
    Tikkanen, Stephanie
    North, Paula
    Burkhart, Craig N.
    Chugani, Harry T.
    Ball, Karen L.
    Pinto, Anna Lecticia
    Loeb, Jeffrey A.
    [J]. PEDIATRIC NEUROLOGY, 2018, 84 : 11 - 20
  • [9] Instruction manual for the ILAE 2017 operational classification of seizure types
    Fisher, Robert S.
    Cross, J. Helen
    D'Souza, Carol
    French, Jacqueline A.
    Haut, Sheryl R.
    Higurashi, Norimichi
    Hirsch, Edouard
    Jansen, Floor E.
    Lagae, Lieven
    Moshe, Solomon L.
    Peltola, Jukka
    Perez, Eliane Roulet
    Scheffer, Ingrid E.
    Schulze-Bonhage, Andreas
    Somerville, Ernest
    Sperling, Michael
    Yacubian, Elza Marcia
    Zuberi, Sameer M.
    [J]. EPILEPSIA, 2017, 58 (04) : 531 - 542
  • [10] An Apparently Classical Case Report of Sturge-Weber Syndrome
    Giannantoni, Nadia Mariagrazia
    Della Marca, Giacomo
    Vollono, Catello
    [J]. CLINICAL EEG AND NEUROSCIENCE, 2015, 46 (04) : 353 - 356