scholarly journals Coexistence of cluster headache and paroxysmal hemicrania: does it exist? A case report and literature review

2009 ◽  
Vol 10 (3) ◽  
pp. 219-223 ◽  
Author(s):  
Nilima D. Shah ◽  
Sanjay Prakash
Cephalalgia ◽  
2003 ◽  
Vol 23 (9) ◽  
pp. 929-930 ◽  
Author(s):  
C Lisotto ◽  
F Mainardi ◽  
F Maggioni ◽  
G Zanchin

The trigeminal autonomic cephalgias (TACs) are characterized by short-lasting unilateral headaches with autonomic features (1). They include four headache disorders, cluster headache (CH), paroxysmal hemicrania (PH), SUNCT syndrome and hemicrania continua (HC). The coexistence of different ipsilateral TACs in the same patient has been previously reported in six published cases (2-6). In five of these patients an association of CH and PH was noted (2-5). The two varieties of attacks occurred separately in three patients, while their simultaneous occurrence was observed in two cases. In another patient the successive occurrence of trigeminal neuralgia, SUNCT syndrome, PH and CH in one active headache period was noted (6). All the reported cases concerned male patients. We describe what we believe to be the first case of coexistence of two different contralateral TACs.


Cephalalgia ◽  
2010 ◽  
Vol 30 (8) ◽  
pp. 975-982 ◽  
Author(s):  
Sanjay Prakash ◽  
Nilima D Shah ◽  
Bhavna V Chavda

Introduction: Response to indomethacin is an essential feature for the diagnosis of both paroxysmal hemicrania (PH) and hemicrania continua (HC). Cluster headache (CH) is widely considered to be a disease unresponsive to indomethacin. Case reports: We report four patients with CH who responded to indomethacin. Two patients, who were refractory to the usual therapy for CH, fulfilled the criteria for chronic CH. Conversely, two patients had a history of episodic CH and showed response to both indomethacin and the usual therapy for CH. Literature review: We also reviewed the literature for the presence of indomethacin response in patients with CH. We noted a large number of cases labeled as CH by the authors which showed a response to indomethacin. Discussion: Many cases of definite or possible CH were wrongly labeled as PH because of patients' responding to indomethacin. Conclusion: The response to indomethacin in patients with CH may not be as immediate as in other indomethacin-responsive headaches, and many patients may need larger doses.


Cephalalgia ◽  
2009 ◽  
Vol 30 (2) ◽  
pp. 233-238 ◽  
Author(s):  
F Antonaci ◽  
E Alfei ◽  
F Piazza ◽  
I De Cillis ◽  
U Balottin

2001 ◽  
Vol 59 (4) ◽  
pp. 944-947 ◽  
Author(s):  
Germany Gonçalves Veloso ◽  
Alexandre Ottoni Kaup ◽  
Mario F Pietro Peres ◽  
Eliova Zukerman

Episodic paroxysmal hemicrania (EPH) is a rare disorder characterized by frequent, daily attacks of short-lived, unilateral headache with accompanying ipsilateral autonomic features. EPH has attack periods which last weeks to months separated by remission intervals lasting months to years, however, a seasonal variation has never been reported in EPH. We report a new case of EPH with a clear seasonal pattern: a 32-year-old woman with a right-sided headache for 17 years. Pain occurred with a seasonal variation, with bouts lasting one month (usually in the first months of the year) and remission periods lasting around 11 months. During these periods she had headache from three to five times per day, lasting from 15 to 30 minutes, without any particular period preference. There were no precipitating or aggravating factors. Tearing and conjunctival injection accompanied ipsilaterally the pain. Previous treatments provided no pain relief. She completely responded to indomethacin 75 mg daily. After three years, the pain recurred with longer attack duration and was just relieved with prednisone. We also propose a new hypothesis: the EPH-cluster headache continuum.


2000 ◽  
Vol 40 (1) ◽  
pp. 54-56 ◽  
Author(s):  
Vincenzo Centonze ◽  
Antonia Bassi ◽  
Vito Causarano ◽  
Lidia Dalfino ◽  
Angelo Centonze ◽  
...  

Cephalalgia ◽  
1987 ◽  
Vol 7 (3) ◽  
pp. 189-192 ◽  
Author(s):  
Jan Hannerz ◽  
Kaj Ericson ◽  
Gustaf Bergstrand

A 62-year-old man with ankylosing spondylitis and with a 3-year history of chronic paroxysmal hemicrania is presented. Because of his ankylosing spondylitis naproxen was prescribed; this decreased the attacks of headache to about 50%. However, treatment with indomethacin and steroids eliminated the attacks completely, the former drug in 24 h but only when the drug was taken; the latter drug was completely effective after a week but with an effect that lasted half a year after the medication was stopped. Orbital phlebography showed changes similar to those previously observed in patients with Tolosa-Hunt syndrome and cluster headache. Venous vasculitis thus seems to be associated with all three disorders and may be a factor of etiologic significance.


Sign in / Sign up

Export Citation Format

Share Document