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Hypnic headache in children
Caterina Cerminara1, Eliana Compagnone, Antonella Coniglio
1University of Rome Tor Vergata, Italy.
Insights
Hypnic headache (HH), a rare sleep-related headache typically seen in older adults, was observed in three children. These pediatric cases suggest HH may occur in younger individuals, potentially requiring updated diagnostic criteria.
Area of Science:
- Neurology
- Pediatric Neurology
- Sleep Medicine
Background:
- Hypnic headache (HH) is a rare disorder characterized by sleep-exclusive headaches, typically affecting the elderly.
- Current diagnostic criteria (ICHD-II) define HH by specific features like nocturnal onset, duration, frequency, and absence of autonomic symptoms.
Observation:
- This report details three pediatric cases presenting with features consistent with hypnic headache.
- The patients, aged 7–11 years, experienced nocturnal headaches with short duration and lacked autonomic symptoms.
Findings:
- The observed cases in children suggest that hypnic headache may manifest in younger populations.
- The clinical presentation in these pediatric patients aligns with established HH characteristics, despite the age difference.
Implications:
- These findings challenge the traditional view of HH as solely an elderly disorder.
- The cases highlight the need to consider HH in the differential diagnosis of headaches in children.
- Further research may lead to revisions in the diagnostic criteria for hypnic headache, particularly for pediatric age groups.
Background:
Hypnic headache (HH) is a rare, short-lasting headache occurring exclusively during sleep and usually affecting the elderly population. According to the ICHD-II diagnostic criteria, HH is characterized exclusively by sleep-related dull headache attacks, either lateralized or bilateral, a recurrence of >15 times per month and a persistence of pain >15 minutes after waking. No autonomic symptoms and no more than nausea, photophobia, or phonophobia are present.
Cases:
We report three children between 7 and 11 years old with HH features. The characteristics of our patient's headache, with particular reference to the nocturnal pattern, the short duration and the absence of autonomic symptoms, lead us to consider the diagnosis of HH.
Conclusions:
Considering the very few cases of HH reported in paediatric age, our cases may expand the clinical spectrum of this disorder, suggesting a possible revision of the diagnostic criteria, with particular regard to the developmental age.
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