Cluster headache

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作者
Arne May
Todd J. Schwedt
Delphine Magis
Patricia Pozo-Rosich
Stefan Evers
Shuu-Jiun Wang
机构
[1] University Medical Center Hamburg-Eppendorf,Department of Systems Neuroscience
[2] Mayo Clinic,Department of Neurology
[3] University Department of Neurology CHR,Neurology Department
[4] Headache and Craniofacial Pain Unit,Department of Neurology
[5] Hospital Universitari Vall d'Hebron,undefined
[6] Headache Research Group,undefined
[7] VHIR,undefined
[8] Universitat Autònoma Barcelona,undefined
[9] Krankenhaus Lindenbrunn,undefined
[10] Taipei Veterans General Hospital,undefined
[11] National Yang-Ming University School of Medicine,undefined
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摘要
Cluster headache is an excruciating, strictly one-sided pain syndrome with attacks that last between 15 minutes and 180 minutes and that are accompanied by marked ipsilateral cranial autonomic symptoms, such as lacrimation and conjunctival injection. The pain is so severe that female patients describe each attack as worse than childbirth. The past decade has seen remarkable progress in the understanding of the pathophysiological background of cluster headache and has implicated the brain, particularly the hypothalamus, as the generator of both the pain and the autonomic symptoms. Anatomical connections between the hypothalamus and the trigeminovascular system, as well as the parasympathetic nervous system, have also been implicated in cluster headache pathophysiology. The diagnosis of cluster headache involves excluding other primary headaches and secondary headaches and is based primarily on the patient's symptoms. Remarkable progress has been achieved in developing effective treatment options for single cluster attacks and in developing preventive measures, which include pharmacological therapies and neuromodulation.
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