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Here is a comprehensive overview of headache classification, drawn from multiple authoritative sources.

Headache: Overview & Classification

What Is Headache?

Headache is among the most common reasons patients seek medical attention and is responsible, globally, for more disability than any other neurologic problem. Diagnosis rests on careful clinical history, neurologic examination, and understanding of the anatomy and physiology of pain pathways. — Harrison's Principles of Internal Medicine 22E, p. 157

The ICHD-3 Framework

The International Classification of Headache Disorders, 3rd Edition (ICHD-3, 2018) — developed by the International Headache Society — is the universal standard. It organizes headaches into four parts: — Bradley and Daroff's Neurology in Clinical Practice

Part 1: Primary Headaches

Headache is the disorder itself — no underlying disease
#Category
1Migraine
2Tension-type headache
3Trigeminal autonomic cephalgias (TACs) (incl. cluster headache)
4Other primary headache disorders

Migraine subtypes (ICHD-3)

  • Without aura
  • With aura (typical, brainstem, hemiplegic, retinal)
  • Chronic migraine
  • Complications: status migrainosus, migrainous infarction, aura-triggered seizure
  • Episodic syndromes associated with migraine (cyclical vomiting, abdominal migraine, benign paroxysmal vertigo)

Tension-type headache subtypes

  • Infrequent episodic
  • Frequent episodic
  • Chronic

Trigeminal Autonomic Cephalgias (TACs)

  • Cluster headache
  • Paroxysmal hemicrania
  • Short-lasting unilateral neuralgiform headache attacks (SUNHA/SUNA)
  • Hemicrania continua

Part 2: Secondary Headaches

Head pain is a symptom of an underlying disorder
CodeAttributed to…
5Trauma or injury to head/neck
6Cranial or cervical vascular disorder (SAH, dissection, CVT, RCVS)
7Nonvascular intracranial disorder (IIH, low CSF pressure, neoplasm)
8Substance use or withdrawal
9Infection (meningitis, encephalitis, systemic infection)
10Disorder of homeostasis (hypoxia, hypertension, dialysis)
11Disorder of cranium, neck, eyes, ears, sinuses, teeth, or TMJ
12Psychiatric disorder

Part 3: Painful Cranial Neuropathies & Other Facial Pain

  • Trigeminal neuralgia, glossopharyngeal neuralgia, other cranial neuralgias

Epidemiology at a Glance (Population-Based Data)

TypePrevalence (%)
Tension-type69% of all headache
Migraine16%
Systemic infection (secondary)63% of secondary
Cluster0.1%
Brain tumor (secondary)0.1%
Source: Olesen et al., The Headaches; cited in Harrison's

Anatomy of Pain: Why Headaches Happen

The key structures involved in primary headache generation: — Harrison's, p. 157–158
  1. Large intracranial vessels & dura mater + peripheral terminals of the trigeminal nerve (the trigeminovascular system)
  2. Trigeminocervical complex — caudal trigeminal nucleus extending into C1–C2 dorsal horns
  3. Rostral pain-processing regions — ventroposteromedial thalamus and cortex
  4. Pain-modulatory systems — hypothalamus and brainstem (influence autonomic features of attacks)
The ventricular ependyma, choroid plexus, pial veins, and most brain parenchyma are not pain-producing.

Red Flags — When to Worry (SNOOP4 features)

These symptoms suggest a serious secondary cause requiring urgent workup: — Harrison's, Table 17-2
Warning Feature
Sudden-onset ("thunderclap") headache
First or worst headache of life
Vomiting that precedes headache
Subacute worsening over days to weeks
Pain triggered by Valsalva (bending, coughing, lifting)
Pain that wakes from sleep or is present on awakening
Onset after age 55
Fever or unexplained systemic signs
Abnormal neurologic examination
Local tenderness (e.g., temporal artery)

Quick Clinical Profiles of the Major Primary Headaches

FeatureMigraineTension-typeCluster
QualityThrobbing/pulsatingDull, pressure ("band")Severe, boring, stabbing
LocationUnilateral (often)BilateralUnilateral, periorbital
Duration4–72 hours30 min – 7 days15–180 minutes
Autonomic featuresN/V, photo/phonophobiaNone/mildIpsilateral tearing, ptosis, rhinorrhea
ActivityWorsened by movementNot worsenedRestlessness/agitation
Sex predominanceFemale > MaleEqualMale > Female (4:1)
TriggersMany (hormones, sleep, food)Stress, postureAlcohol, circadian (nocturnal)

Sources: Harrison's Principles of Internal Medicine 22E, p. 157–158 | Bradley and Daroff's Neurology in Clinical Practice | Neuroanatomy through Clinical Cases, 3rd Ed., p. 165
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