1.Probable Paroxysmal Hemicrania Associated with Holmes-Adie Syndrome.
Yoo Hwan KIM ; Ju Yeon KIM ; Byung Jo KIM
Journal of the Korean Neurological Association 2011;29(4):376-378
No abstract available.
Adie Syndrome
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Paroxysmal Hemicrania
2.Two Cases of Paroxysmal Hemicrania with Response to Rofecoxib.
Jin Kuk DO ; Ji Eun KIM ; Dong Kuck LEE
Journal of the Korean Neurological Association 2003;21(3):304-306
Paroxysmal hemicrania (PH) has been recently defined as an uncommon primary headache. PH is characterized by frequent attacks of severe unilateral pain associated with autonomic symptoms. The attack frequency usually ranges from 5 to 40 attacks per day. PH is characterized by its absolute responsiveness to indomethacin. However, indomethacin is not often well tolerated because of its gastric side effects. We report two patients with PH who could not tolerate indomethacin due to its severe gastric side effects but dramatically responded to rofecoxib.
Headache
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Humans
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Hydrogen-Ion Concentration
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Indomethacin
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Paroxysmal Hemicrania*
3.Bilateral paroxysmal hemicrania with autonomic features in a child: A case report.
Korean Journal of Pediatrics 2009;52(5):619-621
Paroxysmal hemicrania (PH) is rare in children and not widely recognized. It is characterized by pain attacks and associated symptoms and signs similar to those experiencing cluster headaches, but the features have a shorter effect, are more frequent, and respond completely to indomethacin. Some patients with PH may experience slight pain across the midline. There are only four cases of bilateral PH in the literature and it is very rare in children. Here, I report the case of a 10-year-old female with bilateral PH diagnosed by the typical symptoms along with the favorable response to indomethacin therapy.
Child
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Cluster Headache
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Female
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Humans
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Hydrogen-Ion Concentration
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Indomethacin
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Paroxysmal Hemicrania
4.Verapamil-responsive SUNCT Syndrome.
Eun Cheol SONG ; Yong Seok LEE ; Kon CHU ; Dong Wook KIM ; Jung Ju LEE ; Seong Ho PARK
Journal of the Korean Neurological Association 2001;19(4):407-409
SUNCT syndrome is characterized by short-lasting, unilateral, neuralgiform headache attacks, with conjuntival injec-tion and tearing. Distinct from trigeminal neuralgia, cluster headache, or paroxysmal hemicrania, this rare syndrome is SUNCT syndrome is characterized by short-lasting, unilateral, neuralgiform headache attacks, with conjuntival injec-tion and tearing. Distinct from trigeminal neuralgia, cluster headache, or paroxysmal hemicrania, this rare syndrome is generally refractory to various medications. We report a 63-year-old man diagnosed with SUNCT syndrome, whose symptoms were relieved by verapamil. The therapeutic effects of verapamil on SUNCT syndrome remain to be verified by further experiences. (J Korean Neurol Assoc 19(4):407~409, 2001)
Cluster Headache
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Headache
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Humans
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Middle Aged
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Paroxysmal Hemicrania
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SUNCT Syndrome*
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Trigeminal Neuralgia
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Verapamil