eMedicine Specialties > Neurology > Pediatric Neurology

Childhood Migraine Variants: Differential Diagnoses & Workup

Author: Wendy G Mitchell, MD, Professor of Neurology, University of Southern California School of Medicine; Consulting Staff, Division of Child Neurology, Children's Hospital Los Angeles, Los Angeles County-University of Southern California
Contributor Information and Disclosures

Updated: Feb 5, 2009

Differential Diagnoses

Aphasia
Frontal Lobe Syndromes
Brainstem Gliomas
Headache: Pediatric Perspective
Cluster Headache
Inherited Metabolic Disorders
Complex Partial Seizures
Intracranial Hemorrhage
Disorders of Carbohydrate Metabolism
Migraine Headache
Epilepsia Partialis Continua
Migraine Variants
First Seizure: Pediatric Perspective
Focal EEG Waveform Abnormalities
Frontal Lobe Epilepsy

Other Problems to Be Considered

Alternating hemiplegia of childhood
Benign occipital epilepsy of childhood
CADASIL, for alternating hemiplegias presenting in adolescents
Complex partial status epilepticus
Epilepsy: pediatric overview
Ingestions
Intoxications
Organic acidurias

Workup

Laboratory Studies

  • During the first or worst episode, perform appropriate laboratory and neuroradiologic studies to exclude other causes of the symptoms.
  • Laboratory studies generally are not helpful between episodes when a history of multiple, recurrent episodes and complete clearing between episodes exists.
  • Evaluate a child with cyclic vomiting with or without head pain for metabolic disease, particularly mitochondrial cytopathy.
    • Studies performed during attacks have higher yield than those performed while the child is feeling well.
    • During the attack, perform the following investigations: serum lactate, serum pyruvate, urine organic acids, and serum ammonia samples. Samples must be collected carefully and handled appropriately by the laboratory. If suspicion of mitochondrial cytopathy is high, blood may be collected any time to examine the DNA for mitochondrial point mutations and deletions.
  • For aura without headache, the differential diagnosis often includes simple partial (focal) seizures. Therefore, electroencephalography (EEG [sleep-deprived is possible] or video EEG [if episodes are frequent]) may help in the diagnosis.
  • For other migraine variants, EEG generally does not confirm or exclude migraine or other alternatives, since epileptiform EEG changes can be observed in migraineurs.

Imaging Studies

  • Neuroimaging (CT, MRI) is indicated during the first or worst attack that presents with simultaneous focal neurologic deficits or altered mental status and/or if any focal findings persist between attacks. Perform these studies to exclude other acute causes of the symptoms. Neuroimaging is less important if the patient presents during a symptom-free interlude, with a history of multiple attacks with complete recovery. In these patients, the clinician can usually rule out acute, life-threatening conditions and more reasonably make a diagnosis of migraine based on history.
  • During or immediately after an attack, functional neuroimagingmay support the diagnosis, although migraine is most often a clinical diagnosis.
    • Single photon emission computed tomography may show hypoperfusion during an aura or episode.
    • Functional MRI (fMRI), a research technique, also may demonstrate abnormalities of perfusion.
    • Gadolinium-enhanced MRI may show focal enhancement during or immediately after the attack. This can cause confusion with ischemic stroke, inflammatory conditions, or infection.

Other Tests

  • EEG may be abnormal during or immediately after an episode, with slowing in focal or generalized patterns. In general, nonspecific interictal EEG abnormalities, including epileptiform activity, are reported in higher frequencies in migraineurs.
  • Continuous ambulatory or video EEG may be useful in the rare patient with episodic confusion, hallucinations, or focal neurologic deficits; partial seizures or nonconvulsive status epilepticus are included in the differential diagnosis for the attack.

More on Childhood Migraine Variants

Overview: Childhood Migraine Variants
Differential Diagnoses & Workup: Childhood Migraine Variants
Treatment & Medication: Childhood Migraine Variants
Follow-up: Childhood Migraine Variants
References

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Further Reading

Keywords

abdominal migraine, acute confusional migraine, basilar migraine, benign paroxysmal vertigo of childhood, cyclic vomiting of childhood, hemiplegic migraine, migraine, migraine aura without headache, ophthalmoplegic migraine, vascular headache, childhood migraine variants, migraine in children

Contributor Information and Disclosures

Author

Wendy G Mitchell, MD, Professor of Neurology, University of Southern California School of Medicine; Consulting Staff, Division of Child Neurology, Children's Hospital Los Angeles, Los Angeles County-University of Southern California
Wendy G Mitchell, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Pediatrics, American Epilepsy Society, Child Neurology Society, and International Child Neurology Association
Disclosure: Questcor Honoraria Consulting

Medical Editor

James J Riviello Jr, MD, George Peterkin Endowed Chair in Pediatrics, Professor of Pediatrics, Section of Neurology and Developmental Neuroscience, Professor of Neurology, Peter Kellaway Section of Neurophysiology, Baylor College of Medicine; Chief of Neurophysiology, Director of the Epilepsy and Neurophysiology Program, Texas Children's Hospital
James J Riviello Jr, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Kenneth J Mack, MD, PhD, Senior Associate Consultant, Department of Child and Adolescent Neurology, Mayo Clinic
Kenneth J Mack, MD, PhD is a member of the following medical societies: American Academy of Neurology, Child Neurology Society, Phi Beta Kappa, and Society for Neuroscience
Disclosure: Nothing to disclose.

CME Editor

Selim R Benbadis, MD, Professor, Director of Comprehensive Epilepsy Program, Departments of Neurology and Neurosurgery, University of South Florida School of Medicine, Tampa General Hospital
Selim R Benbadis, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Sleep Medicine, American Clinical Neurophysiology Society, American Epilepsy Society, and American Medical Association
Disclosure: Nothing to disclose.

Chief Editor

Amy Kao, MD, Assistant Professor, Department of Pediatrics, Division of Pediatric Neurology, Department of Neurology, Oregon Health and Science University; Consulting Staff, Shriners Hospital for Children
Amy Kao, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Pediatrics, American Epilepsy Society, and Child Neurology Society
Disclosure: Nothing to disclose.

 
 
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