Episodic parieto-occipital idiopathic stabbing headache-like pain: a case report
نویسندگان
چکیده
منابع مشابه
Abdominal and lower back pain in pediatric idiopathic stabbing headache.
Idiopathic stabbing headache (ISH) is a primary headache syndrome characterized by transient, sharp, stabbing pains located in the first division of the trigeminal nerve. Reports of pediatric ISH are rare, and extracephalic pain in pediatric ISH is extremely rare. Here we report the case of a 7-year-old male patient suffering from frequent, short, stabbing headache, which was occasionally assoc...
متن کاملThe use of etoricoxib to treat an idiopathic stabbing headache: a case report
According to the International Headache Society, idiopathic stabbing headache (ISH), an indomethacin-responsive headache syndrome, is a paroxysmal disorder of short duration manifested as head pain occurring as a single stab or a series of stabs involving the area supplied in the distribution of the first division of the trigeminal nerve. Stabs last for approximately a few seconds, occurring an...
متن کاملIdiopathic stabbing headache associated with monocular visual loss.
BACKGROUND Idiopathic stabbing headache, which is a brief, sharp, severe jabbing pain that is confined to the head, responds well to treatment with indomethacin sodium. It may occur as a primary entity but more likely is associated with other types of headache, including migraine. SETTING Emergency department of a teaching hospital. PATIENT A 27-year-old man presented to the emergency depar...
متن کاملStabbing headache in a teenager.
CLINICAL HISTORY A 17-year-old adolescent girl was seen with a 4-year history of head pain which, initially, was occasional. After gradually increasing in frequency during the last year, this pain has been occurring daily. She describes a stabbing pain in the left or right temple lasting seconds. She often has multiple recurring pains (pain for seconds, brief remission, recurrent pain, etc) wit...
متن کاملHeadache: A Presentation of Pompe Disease; A Case Report
Pompe disease, also termed glycogen storage disease type II or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (GAA), the glycogen degrading lysosomal enzyme. As a result, massive lysosomal glycogen deposits in the numerous organs including the muscles. In Pompe disease weakness of truncal muscles is a prominent presentation which results in respiratory failure a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: The Journal of Headache and Pain
سال: 2002
ISSN: 1129-2369,1129-2377
DOI: 10.1007/s101940200016