Headache in a variety of forms is one of the most common complaints presenting to the clinician.  A new classification of headache has been proposed by the International Headache Society (IHS) (Table 1).1    The classification system is summarized in Table 1.1


Table 1. International Headache Society Classification of Headache

 

1.             Migraine

1.1           Migraine without aura

1.2           Migraine with aura

1.3           Childhood periodic syndromes

1.4           Retinal migraine

1.5           Complications of migraine

1.6           Probable migraine

 

2.             Tension-type headache (TTH)

2.1           Infrequent Episodic tension-type headache

2.2           Frequent episodic tension-type headache

2.3.           Chronic tension-type headache

2.4           Probable tension-type headache

 

3.             Cluster headache and other trigeminal autonomic cephalalgias

3.1           Cluster headache

3.2           Paroxysmal hemicrania

3.3           Short-lasting unilateral neuralgiform headache attacks with Conjunctival injection and Tearing (SUNCT)

3.4             Probable trigeminal autonomic cephalalgia

 

4.             Other primary headaches

4.1           Primary stabbing headache

4.2           Primary cough headache

4.3           Primary exertional headache

4.4           Primary headache associated with sexual activity

4.5           Hypnic headache

4.6           Primary thunderclap headache

4.7            Hemicrania continua

4.8            New daily-persistent headache (NDPH)

 

5.             Headache attributed to head and/or neck trauma

5.1           Acute post-traumatic headache

5.2           Chronic post-traumatic headache

5.3            Acute headache attributed to whiplash injury

5.4            Chronic headache attributed to whiplash injury

5.5            Headache attributed to traumatic intracranial haematoma

5.6            Headache attributed to other head and/or neck trauma

5.7            Post-craniotomy headache

 

6.             Headache attributed to cranial or cervical vascular disorder

6.1           Headache attributed to ischemic stroke or transient ischemic attack

6.2           Headache attributed to non-traumatic intracranial haemorrhage

6.3           Headache attributed to unruptured vascular malformation

6.4           Headache attributed to arteritis

6.5           Carotid or vertebral artery pain

6.6           Headache attributed to cerebral venous thrombosis

6.7           Headache attributed to other intracranial vascular disorder

 

7.             Headache attributed to non-vascular intracranial disorder

7.1           Headache attributed to high cerebrospinal fluid pressure

7.2           Headache attributed to low cerebrospinal fluid pressure

7.3           Headache attributed to non-infectious inflammatory disease

7.4           Headache attributed to intracranial neoplasm

7.5           Headache attributed to intrathecal injection

7.6           Headance attributed to epileptic seizure

7.7           Headache attributed to Chiari malformation type I

7.8            Syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis

7.9            Headache attributed to other non-vascular intracranial disorder

8.             Headache associated to a substance2 or its withdrawal

8.1           Headache induced by acute substance use or exposure

8.2           Medication-overuse headache (MOH)

8.3           Headache as an adverse event attributed to chronic medication

8.4           Headache attributed to substance withdrawal

 

9.             Headache attributed to infection

9.1           Headache attributed to intracranial infection

9.2           Headache attributed to systemic infection

9.3           Headache attributed to HIV/AIDS

9.4            Chronic post-infection headache

 

10.           Headache attributed to disorder of homoestasis

10.1         Headache attributed to hypoxia

10.2         Dialysis headache

10.3         Headache attributed to arterial hypertension

10.4         Headache attributed to hypothyroidism

10.5         Headache attributed to fasting

10.6         Cardiac cephalalgia

10.7           Headache attributed to other disorder of homoestasis

 

11.           Headache or facial pain attributed to disorder of cranium, neck, eyes, ears, nose, sinuses, teeth, mouth, or other facial or cranial structures

11.1         Headache attributed to disorder of cranial bone

11.2         Headache attributed to disorder of neck

11.3         Headache attributed to disorder of eyes

11.4         Headache attributed to disorder or ears

11.5         Headache attributed to rhinosinusitis

11.6         Headache attributed to disorder of teeth, jaws, or related structures

11.7         Headache or facial pain attributed to a temporomandibular joint (TMJ) disorder

11.8          Headache attributed to other disorder of cranium, neck, eyes, ears, nose, sinuses, teeth, mouth or other facial or cervical structures

 

12.           Headache attributed to psychiatric disorder

12.1           Headache attributed to somatisation disorder

12.2           Headache attributed to psychotic disorder

 

13.            Cranial neuralgias and central causes of facial pain

13.1         Trigeminal neuralgia

13.2           Glossopharyngeal neuralgia

13.3         Nervus intermedius neuralgia

13.4         Superior laryngeal neuralgia

13.5         Nasociliary neuralgia

13.6         Supraorbital neuralgia

13.7         Other terminal branch neuralgias

13.8           Occipital neuralgia

13.9           Neck-tongue syndrome

13.10         External compression headache

13.11         Cold-stimulus headache

13.12         Constant pain caused by compression, irritation or distortion of cranial nerves or upper cervical roots by structural lesions

13.13        Optic neuritis

13.14        Ocular diabetic neuropathy

13.15         Head or facial pain attributed to herpes zoster

13.16         Tolosa Hunt syndrome

13.17         Ophthalmoplegic ‘migraine’

13.18         Central causes of facial pain

13.19        Other cranial neuralgia or other centrally mediated facial pain

 

14.           Other headache, cranial neuralgia, central or primary    facial pain

This chapter addresses the neuro‑ophthalmologic aspects of migraine and provides a brief review of other common headaches, facial and ocular pains. Migraine is a periodic and paroxysmal protean disorder that affects more than 17% of women and 6% of men in the United States.2, 3  It is estimated that the lifetime prevalence of migraine in women is 99% and the lifetime prevalence in men is 93%.4  Neuro‑ophthalmologic symptoms and signs are common in migraine and should be recognized by the clinician. The term  hemicrania evolved from a variety of older descriptions and was one of the first names for this disorder; this was later contracted by the French in the 13th century to the word "migraine."  More than 300 years ago, Thomas Willis wrote the first modern description of migraine and its possible causes. Historical figures believed to have had migraine include Julius Caesar, Emmanuel Kant, Alexander Pope, and Sigmund Freud. Throughout the 18th and 19th centuries descriptions of the clinical phenomena and suggestions for therapy continued to appear in the writings of many prominent men in the medical professions. Sacks5 pays homage to Edward Liveing's masterful treatise On Megrim, Sick Headache, and Some Allied Disorders (1873) as an unequaled description of the disorder.  Further detailed clinical descriptions are found in the writings of Gowers.6

In contemporary medicine, Dalessio,  Goadsby, Raskin, Sacks, Silberstein, Lipton, Stewart, Saper, and Welch,  are among those who could be singled out for their contributions to the study of migraine.  One central theme seems to decry the simplistic view that migraine is defined by a unilateral (hemicranial) headache.  As Sacks5 wrote, "It is necessary to state that headache is never the sole symptom of a migraine, nor indeed is it the necessary feature of migraine attacks."  Another quote emphasizes this belief:  "Migraine is diagnosed by the entire history, not by physical findings or by the presence of headache alone".7  It is unfortunate that many have limited their concept of migraine to a stereotyped syndrome of visual disturbance followed by unilateral throbbing headache, which is diagnosed by the response to ergot preparations.  Migraine gives rise to a number of well‑recognized syndromes, as well as a variety of "equivalents" less commonly considered as migraine.  The symptom‑complexes or syndromes of migraine include migraine without aura, migraine with aura, ophthalmoplegic migraine, retinal migraine, as well as the others listed in

Table 1.  The clinical features of migraine will be discussed according to the formal criteria published by the International Headache Society (IHS) in 2004.1

Other conditions and syndromes discussed include cluster headache, trigeminal neuralgia, atypical facial pain, temporal arteritis, and the headaches produced by intracranial mass lesions, muscle contraction, trauma, vascular anomalies, and ocular lesions.

 

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