Case 494 · ICHD-3 7.4.3
7.4.3 Headache attributed to hypothalamic or pituitary hyper- or hyposecretion
- 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: Sex/Age: Male, 38 years History: Hypertension for 2 years, no other relevant history Medication: Antihypertensives (partially controlled) History of Present Illness (HPI): Main symptom: Constant frontal headache for 3 months Characteristics of the pain: Location: Bilateral frontal and retro-orbital Intensity: 6-7/10 Quality: Deep pressure Aggravating factors: Forward head tilt No response to common analgesics Associated symptoms: Intermittent double vision Progressive loss of peripheral vision Increase in the size of feet and hands Erectile dysfunction Physical/Neurological Examination: Physical appearance: Macrognathia, broadening of facial features Visual field test: Bitemporal hemianopsia Neurological: Partial paralysis of the right oculomotor nerve Other: Enlargement of extremities, thickened skin Complementary Exams: Magnetic Resonance Imaging of the Sella Turcica: Pituitary macroadenoma (2.5 cm) with suprasellar extension Laboratory: GH: 15 ng/mL (elevated) IGF-1: 780 ng/mL (elevated) Glucose tolerance test: GH not suppressed Prolactin: 35 ng/mL (slightly elevated)
Report this case — e.g. suspected re-identification risk.