Abstract

BackgroundShort-lasting unilateral neuralgiform headache with conjunctival injection and tearing (SUNCT) and short-lasting unilateral neuralgiform attacks with cranial autonomic features (SUNA) are rare primary headache syndromes characterized by spontaneous or triggered attacks of unilateral, brief, multiple, orbitofrontal pain associated with ipsilateral autonomic features. SUNCT is considered as a subset of SUNA. In SUNA, there may be cranial autonomic symptoms other than conjunctival injection and lacrimation, or either of two is present. SUNCT/SUNA can be triggered immediately after or at the decrescendo phase of the ongoing attack without any intervening refractory period. Refractory period is usually present in trigeminal neuralgia. Absent refractory period is thought to reliably differentiate SUNCT/SUNA from trigeminal neuralgia and has been proposed for inclusion into the International Classification of Headache Disorders (ICHD) diagnostic criteria for SUNCT.Case reportsWe report three patients of SUNCT syndrome with preserved intervening refractory period of variable duration observed at different times.DiscussionTrigeminal neuralgias with autonomic features, SUNA and SUNCT share a common pathophysiological mechanism and actually represent a continuum. It is well known that patient with trigeminal neuralgia may transform into SUNCT/SUNA. Similarly, being a continuum, the presence or the absence of refractory period and its duration may change in a patient with SUNCT/SUNA at different time points.ConclusionThe presence of refractory period should not exclude the diagnosis of SUNCT in a patient with other clinical features suggestive of SUNCT.Electronic supplementary materialThe online version of this article (doi:10.1007/s10194-011-0412-7) contains supplementary material, which is available to authorized users.

Highlights

  • Background Short-lasting unilateral neuralgiform headache with conjunctival injection and tearing (SUNCT) and short-lasting unilateral neuralgiform attacks with cranial autonomic features (SUNA) are rare primary headache syndromes characterized by spontaneous or triggered attacks of unilateral, brief, multiple, orbitofrontal pain associated with ipsilateral autonomic features

  • Case reports We report three patients of SUNCT syndrome with preserved intervening refractory period of variable duration observed at different times

  • The presence of refractory period should not exclude the diagnosis of SUNCT in a patient with other clinical features suggestive of SUNCT

Read more

Summary

Discussion

Clinical features of our cases conform to diagnostic criteria of SUNCT (ICHD 2nd ed) and does not comply with diagnosis of migraine, paroxysmal hemicrania and cluster headache [3]. Trigeminal autonomic reflex with central disinhibition of variable extent is thought to produce a continuum of trigeminal neuralgia, SUNA and SUNCT [1] Most patients with these headaches show variation in pain intensity, attack frequency and severity of autonomic symptoms. SUNCT caused by ipsilateral superior cerebellar artery vascular loop near the root entry zone of trigeminal nerve is rare [10, 11]. These aberrant vessels can be delineated by special MRI techniques like fast imaging employing steady-state acquisition (FIESTA).

Conclusion
Introduction
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call