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Published on: June 2, 2014
Migraine-like headache and status migrainosus as attacks of multiple sclerosis in a child
Paolo Mariotti1, Viviana Nociti, Alessandro Cianfoni
1Unit of Child Neuropsychiatry, Institute of Neurology, Catholic University of Rome, Rome, Italy.
Insights
Headache can be an early symptom of pediatric multiple sclerosis (MS), even presenting as the sole symptom during relapses. This case highlights migraine-like headaches linked to specific MS lesion locations in a child.
Area of Science:
- Neurology
- Pediatric Neurology
- Neuroimmunology
Background:
- Headache is more common at the onset of pediatric multiple sclerosis (MS) than in adults.
- Headache as an isolated relapse symptom is infrequent in both pediatric and adult MS.
Observation:
- A 5-year-old child presented with MS, experiencing migraine-like headaches at disease onset and two subsequent relapses.
- The initial relapse included headache fulfilling criteria for status migrainosus.
Findings:
- Lesion localization in the midbrain, periaqueductal gray matter, and upper cervical cord, along with meningeal reactions and brain swelling, correlated with migraine-like headaches.
- The improvement of headaches following immunomodulatory treatment for MS suggests a direct relationship.
Implications:
- This case underscores the potential for headache, particularly migraine-like presentations, as a key symptom in pediatric MS.
- Understanding lesion-symptom correlations is crucial for diagnosing and managing MS in children.
- Further research into the mechanisms linking MS pathology to headache presentations is warranted.
Abstract:
The incidence of headache at the onset of relapsing-remitting pediatric multiple sclerosis (MS) is more frequent than in the adult MS population, but headache as the only symptom of a relapse, both in adults and children, is unusual. Here we describe the case of a 5-year-old child who developed MS and in whom migraine-like headache was the presenting symptom at both the onset of the disease and the following 2 relapses. Moreover, the first relapse was characterized by the occurrence of headache that fulfilled the time criteria for status migrainosus. The presence of headache during MS might depend on the anatomic distribution of lesions. In our case, the demyelinating plaques localized in the midbrain, the periaqueductal gray matter, and the upper cervical cord together with the meningeal reaction and the diffuse brain swelling might have caused the onset of migraine-like headache and the status migrainosus. The causal relationship between headache and MS attacks, in our case, was also confirmed by the improvement of headache under immunomodulatory treatment for MS, because it is known that headache is often caused or exacerbated by interferon beta therapy.
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