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Anti-homer-3 Antibody Encephalitis in a 10-Year-Old Child: Case Report and Review of the Literature.
- Source :
-
Frontiers in neurology [Front Neurol] 2022 Jun 13; Vol. 13, pp. 929778. Date of Electronic Publication: 2022 Jun 13 (Print Publication: 2022). - Publication Year :
- 2022
-
Abstract
- Objective: We present a rare case with anti-Homer-3 antibodies positive encephalitis in the youngest patient ever identified and reviewed the literature.<br />Case Report: A 10-year-old, Chinese boy came for evaluation of a 2-week history of cognitive impairment, irritability, dysarthria, and cautious gait. The neurological examination was consistent with the pan-cerebellar syndrome and encephalopathy. Cerebrospinal fluid (CSF) was inflammatory with increased leukocytes. Magnetic resonance imaging of the brain showed hyperintensities in both cerebellar hemispheres and vermis in Fluid-attenuated inversion recovery (FLAIR) and T2- weighted sequences. Infectious disorders were ruled out, but positivity for anti-Homer-3 antibodies was detected in the CSF, but not in the serum. Additionally, low titers of voltage-gated calcium channel (VGCC) antibodies were found in the serum. Treatment with intravenous (IV) corticosteroids did not provide meaningful clinical improvement; however, the patient achieved almost complete recovery (modified Ranking Scale score: 1) following IV immunoglobulin.<br />Conclusion: Anti-Homer-3 cerebellar ataxia with encephalopathy should be considered within the differential diagnosis of acute inflammatory cerebellar disease in children and it may coexist with VGCC antibodies.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflictof interest.<br /> (Copyright © 2022 Kuang, Baizabal-Carvallo, Mofatteh, Xie, Wang and Chen.)
Details
- Language :
- English
- ISSN :
- 1664-2295
- Volume :
- 13
- Database :
- MEDLINE
- Journal :
- Frontiers in neurology
- Publication Type :
- Report
- Accession number :
- 35769364
- Full Text :
- https://doi.org/10.3389/fneur.2022.929778