Case 210 · ICHD-3 3.1.2
3.1.2 Chronic cluster headache
- Origin
- Synthetic
- Language
- English — also available in German
- Contributed by
- Imported case — HeadAI synthetic vignettes (de Andrade JBC, da Silva Costa TB, Vasconcelos JL, Lopes TLM, Balsells MD, Cristofolini VL, Querobin SO, Filho FMR. Validation of an AI-based platform for structured diagnosis of headache disorders using ICHD-3 criteria. BMC Neurology 25, 489 (2025). doi:10.1186/s12883-025-04473-1. Dataset: Andrade J. Head.AI Platform. Mendeley Data, V2 (2025). doi:10.17632/4fms6cw2s5.2)
Anamnesis
Identification: Male patient, 45 years old, Caucasian, plumber.
History of Present Illness: The patient reports a history of intense, unilateral, periorbital and temporal headache, lasting 30 to 90 minutes, occurring on average 3 to 4 times a day for approximately 2 years. The attacks are accompanied by tearing, nasal congestion, eyelid ptosis, and psychomotor agitation. He states that the pain is so intense that it causes him to walk or rock his body during the attacks. There is no report of aura or prodromal symptoms. The patient mentions that the episodes occur in clustering periods (bouts), with short or absent remission intervals (less than 1 month), characterizing the chronic form of the disease.
Past Medical History: Well-controlled arterial hypertension with medication. Denies history of migraine or other primary headaches.
Physical Examination:
General: Patient conscious, oriented, emaciated (reports loss of appetite due to the attacks).
Neurological: Mild left eyelid ptosis during the attack, without other focal deficits.
Ophthalmological: Pupils are isocoric, photoreactive, without fundoscopic changes.
ENT: Nasal mucosa hyperemic on the left during the attack.
Complementary Exams:
Cranial magnetic resonance imaging: Normal, without structural lesions.
Magnetic resonance angiography: No significant vascular changes.
Report this case — e.g. suspected re-identification risk.