Alice in Wonderland syndrome: a novel neurological presentation of Zika virus infection

被引:0
作者
Alberto E. Paniz-Mondolfi
José Giraldo
Alfonso J. Rodríguez-Morales
Oriana Pacheco
Germán Y. Lombó-Lucero
Juan D. Plaza
Fabio J. Adami-Teppa
Alejandra Carrillo
Carlos E. Hernandez-Pereira
Gabriela M. Blohm
机构
[1] Clínica IDB Cabudare. Instituto de Investigaciones Biomédicas IDB,Department of Infectious Diseases and Tropical Medicine
[2] Instituto de Estudios Avanzados (IDEA),Laboratorio de Señalización Celular y Bioquímica de Parásitos
[3] Instituto Venezolano de los Seguros Sociales (IVSS),Directorate of Health
[4] Hospital Internacional Barquisimeto,Department of Ophtalmology and Neuro
[5] Colombian Collaborative Network on Zika (RECOLZIKA),ophtalmology
[6] Universidad Tecnologica de Pereira,Public Health and Infection Research Group, Faculty of Health Sciences
[7] Venezuelan Science Incubator,Infectious Diseases Research Incubator and the Zoonosis and Emerging Pathogens Regional Collaborative Network
[8] Universidad Centroccidental Lisandro Alvarado,Health Sciences Department, College of Medicine
[9] Universidad Nacional Experimental “Francisco de Miranda”,Health Sciences Department, College of Medicine
[10] Clínica IDB Cabudare. Instituto de Investigaciones Biomédicas IDB,Division of Neuroradiology, Department of Radiology
[11] University of Florida,Department of Biology, College of Liberal Arts and Sciences
[12] University of Florida,Emerging Pathogens Institute
来源
Journal of NeuroVirology | 2018年 / 24卷
关键词
Zika virus; Alice in Woderland syndrome; Viral; Metamorphopsia;
D O I
暂无
中图分类号
学科分类号
摘要
Zika virus (ZIKV) is a flavivirus endemic in Africa and Southern Asian countries, which has recently emerged in unprecedented epidemic proportions around the world. Although ZIKV infection is often asymptomatic or distinguished by non-specific influenza-like symptoms, an increase in its pathogenicity and biological behavior has been the hallmark of the current pandemic. Increasing evidence suggests that neurotropic strains of ZIKV have evolved from less pathogenic strains of the virus. Neurological manifestations of ZIKV infection include a spectrum of congenital and non-congenital clinical entities, however visual somatosensory perceptual disorders have not been recorded to date. Herein, we report a case of a 15-year-old female who presented with a constellation of perceptual symptoms (metamorphopsia, telopsia, and pelopsia) following acute ZIKV infection. Although such symptoms may have originated from direct viral injury, a post-ZIKV autoimmune reaction to previously unexposed neuronal surface antigens or through molecular mimicry cannot be excluded. The development of Alice in Wonderland syndrome in our patient highlights the ever-increasing expanding spectrum of neurological symptoms associated to ZIKV infection.
引用
收藏
页码:660 / 663
页数:3
相关论文
共 80 条
  • [1] Araujo AQ(2006)The HTLV-1 neurological complex Lancet Neurol 5 1068-1076
  • [2] Silva MT(2016)Zika virus infection with prolonged maternal viremia and fetal brain abnormalities N Engl J Med 374 2142-2151
  • [3] Driggers RW(2017)Alice in Wonderland syndrome: A Historical and Medical Review Pediatr Neurol 77 5-11
  • [4] Ho CY(2013)The Alice in Wonderland syndrome Prog Brain Res 206 143-156
  • [5] Korhonen EM(2017)NMDAR encephalitis following herpes simplex virus encephalitis Curr Infect Dis Rep 19 1-209
  • [6] Kuivanen S(2013)Virus infection, antiviral immunity, and autoimmunity Immunol Rev 255 197-19
  • [7] Jääskeläinen AJ(2016)CSF herpes virus and autoantibody profiles in the evaluation of encephalitis Neurol Neuroimmunol Neuroinflamm 3 e245-958
  • [8] Smura T(1996)Flavivirus-induced up-regulation of MHC class I antigens; implications for the induction of CD8+ T-cell-mediated autoimmunity Immunol Rev 152 5-1059
  • [9] Rosenberg A(2016)Minimal immune determinants connect Zika virus, human Cytomegalovirus, andToxoplasma gondiito microcephaly-related human proteins American Journal of Reproductive Immunology 77 e12608-474
  • [10] Hill DA(2016)Alice in Wonderland Syndrome: A Clinical and Pathophysiological Review Biomed Res Int 2016 951-327