Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Pseudomigraine with pleocytosis].

Gabriela S Pariso1, Virginia L Parisi, Gabriel G Persi

  • 1Departamento de Neurología, Sanatorio de la Trinidad-Mitre, Buenos Aires.

Medicina
|September 19, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Levodopa-Induced dyskinesia in Latin America: Prevalence and associated clinical factors in the LARGE-PD cohort.

Journal of Parkinson's disease·2026
Same author

Protective or Pathogenic? Kinase activity and the neurodevelopmental origins of G2019S LRRK2-Associated Parkinson's disease.

Parkinsonism & related disorders·2025
Same author

EPIDEMIOLOGY OF LEVODOPA-INDUCED DYSKINESIA: PREVALENCE AND ASSOCIATED CLINICAL FACTORS IN LATIN AMERICA.

medRxiv : the preprint server for health sciences·2025
Same author

Sex differences in the diagnosis latency of Parkinson's disease in Latin America.

Parkinsonism & related disorders·2025
Same author

Differences and contributors to global cognitive performance in the underrepresented Latinx Parkinson's disease population.

The Clinical neuropsychologist·2025
Same author

Case report: CSF hypotension secondary to a free syringo-subarachnoid-peritoneal shunt.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery·2024
Same journal

Detection of VIM-3 in oral squamous cell carcinomas: methodological limitations.

Medicina·2026
Same journal

The importance of specific antibodies in VIM-3 research: addressing a key methodological flaw.

Medicina·2026
Same journal

[From the right to be cared for to the duty to care: Legal bases for the implementation of palliative care in Argentina].

Medicina·2026
Same journal

[Surrogacy].

Medicina·2026
Same journal

[The misunderstandings in interpreting the "diagnostic superiority of Artificial Intelligence" and the explainable Artificial Intelligence].

Medicina·2026
Same journal

[Artificial intelligence in medicine: between algorithmic opacity and clinical responsibility].

Medicina·2026
See all related articles

Transient headache and neurological deficits with cerebrospinal fluid lymphocytosis or pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis (HaNDL) is a rare syndrome. This case report details a patient experiencing migraine with pleocytosis and transient deficits, highlighting the importance of differential diagnosis.

Area of Science:

  • Neurology
  • Neuroscience
  • Clinical Neurology

Background:

  • Transient headache and neurological deficits with cerebrospinal fluid lymphocytosis or pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis (HaNDL) is a rare neurological syndrome.
  • Characterized by recurrent headaches, reversible neurological deficits, and lymphocytic pleocytosis in cerebrospinal fluid (CSF).
  • Etiology remains largely unknown despite proposed vascular, infectious, immunological, and calcium channelopathy mechanisms.

Observation:

  • A case of a 28-year-old female presenting with recurrent migraine accompanied by pleocytosis.
  • The patient also experienced a confusional syndrome and transient neurological deficits.
  • Clinical remission was observed within two months.

Findings:

Related Experiment Videos

  • The presented case aligns with the diagnostic criteria for HaNDL syndrome.
  • The patient's symptoms, including migraine, pleocytosis, and transient neurological deficits, resolved spontaneously.
  • This case underscores the variability in presentation and the importance of recognizing HaNDL.
  • Implications:

    • Accurate diagnosis of HaNDL syndrome is crucial for appropriate patient management.
    • Considering HaNDL in the differential diagnosis can prevent unnecessary investigations and treatments.
    • Further research into the etiopathogenesis of HaNDL is warranted to improve understanding and treatment strategies.