Case 436 · ICHD-3 6.9
6.9 Headache attributed to pituitary apoplexy
- 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, 58 years old.
Background: Known non-functioning pituitary adenoma (incidentally diagnosed 2 years ago on MRI), arterial hypertension.
Medications: Antihypertensives (no recent use of anticoagulants or antiplatelets).
History of Present Illness (HPI): Main symptom: Sudden and intense headache (10/10) for 12 hours, described as "stabbing" retro-orbital and frontal pain.
Characteristics:
Onset: Abrupt, during rest.
Aggravation: Associated with nausea/vomiting and worsens with head movements.
Associated symptoms:
Diplopia (right oculomotor nerve paralysis).
Postural hypotension and drowsiness (suspected acute adrenal insufficiency).
Physical/Neurological Examination:
General: Hypotension (BP 90/60 mmHg), tachycardia.
Neurological:
Right eyelid ptosis and mydriasis (III nerve paresis).
Bitemporal hemianopsia (chiasmatic compression).
Fluctuating level of consciousness (Glasgow Coma Scale 14).
Complementary Exams:
Brain MRI: Sudden increase in pituitary adenoma size (1.8 cm → 3.0 cm) with signs of intralesional hemorrhage (hyperintense on T1) and optic chiasm compression.
Laboratory:
Hormonal: Low serum cortisol (3 µg/dL), reduced TSH and free T4.
Electrolytes: Hyponatremia (Na+ 125 mEq/L).
Report this case — e.g. suspected re-identification risk.