Transient Headache and Neurological Deficits with cerebrospinal fluid Lymphocytosis (HaNDL) syndrome in children: case report and narrative review
HaNDL is a rare self-limiting syndrome affecting both adults and children. The etiology is unknown, but autoimmune mechanisms have been proposed. HaNDL is a diagnosis of exclusion: differential diagnoses include stroke, tumors, epilepsia, neuro-infective disorders, autoimmune encephalitis, vasculitis, hemiplegic migraine and migraine with aura. Usually, HaNDL episodes last less than 3 months; therapy is symptomatic. The diagnostic work out includes CSF analysis, neuroimaging and EEG. The treatment is symptomatic, and the course is self-limiting, usually resolving within 3 months.
Authors
- Cristina Vassia
- Barbara Lauria
- Claudia Bondone (ORCID: https://orcid.org/0000-0003-4120-2533)
- Emanuele Castagno (ORCID: https://orcid.org/0000-0001-7756-5075)
- Giulia Grasso (ORCID: https://orcid.org/0000-0002-4255-5472)
- Roberta Rossi (ORCID: https://orcid.org/0000-0001-8408-1124)
- Antonia Versace (ORCID: https://orcid.org/0000-0001-5581-5491)
- Giulia Abrate
Institutions
- Ospedale Regina Margherita (IT)
- Department of Public Health (US)
Publication Details
- Journal
- The Italian Journal of Pediatrics/Italian journal of pediatrics
- Published
- 2025-11-19
- DOI
- https://doi.org/10.1186/s13052-025-02139-9
- Primary Topic
- Neurological Complications and Syndromes
- Type
- article
- Field-Weighted Citation Impact
- 0.00