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HaNDL-syndrom som en sjælden årsag til migrænelignende hovedpine og neurologiske udfald hos en teenager

Forfatter(e)
Tamo Sultan & Jens Erik Klint Nielsen

Pædiatrisk Afdeling, Sjællands Universitetshospital, Roskilde

 

Ugeskr Læger 2020;182:V09190515

Reference: 
Ugeskr Læger 2020;182:V09190515
Blad nummer: 

Tamo Sultan & Jens Erik Klint Nielsen:

A teenager with a rare cause of migraine-like headaches and neurological deficits – syndrome of transient headache and neurologic deficits with cerebrospinal fluid lymphocytosis

Ugeskr Læger 2020;182:V09190515

In this case report, a 14-year-old male presented with episodes of migraine-like headaches preceded by unilateral hemiparaesthesia, hemiparesis, confusion, and dysphasia with the last two lasting more than four hours. The cerebrospinal fluid (CSF) showed lymphocytosis with no detectable aetiology, neuroimaging was normal, and an electroencephalogram showed diffuse slowing. The patient was diagnosed with headache associated with neurologic deficits and CSF lymphocytosis, i.e. syndrome of transient headache and neurologic deficits with cerebrospinal fluid lymphocytosis. The condition is a rare disorder, especially in children. Normally, a complete remission takes place within few weeks to months without treatment.

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