Abbreviations: SM status migrainosus, CNS central nervous system, CH, cluster headache, AP Adie's pupil, CT computerized tomography, MRI/MRA, magnetic resonance imaging and angiography ( Headache. 2002;42:793-795) Status migrainosus (SM) is a migraine variant characterized by severe headache persisting beyond three days sometimes accompanied by nausea and vomiting. 1 Although a serious central nervous system (CNS) pathology is usually absent, exceptional patients may exhibit arterial segmental stenosis and dilatations visualized by cerebral arteriography suggesting the presence of an underlying inflammatory angiopathy. 2 In this paper, a patient is described with acute onset of prolonged, pulsatile left frontal and orbital headache associated with ipsilateral pupillary dilatation lasting for several months and followed by the development of new headache and contralateral pupillary dilatation. There was no evidence of a structural CNS lesion, and by clinical examination, she had Adie's pupil and polyneuropathy (Adie's syndrome).
CASE REPORTA 27-year-old female was sent for neurological evaluation because of headache, blurred vision, and dilatation of the left pupil. She reported the abrupt onset of severe left frontal and orbital headache for 2 months prior, with continuous headaches since then. She reported an 8-year history of similar headaches, but never associated with blurred vision or with di-lated pupils. Her previous headaches were less intense and did not last more than 1 or 2 days on the average. She had no symptoms of systemic or infectious illnesses. She had no history of syncope or postural hypotension and no history of bladder or bowel disturbance. She had no dry mouth or eyes. Her past medical history was significant for hypertension and anxiety disorder treated with hydrochlorothiazide 25 mg qid and paroxetine 20 mg qid. She had a sister with migraine.Her blood pressure was 160/100, her apical pulse was 78 per minute, her respiratory rate was 20 per minute, and she was afebrile. General physical examination was normal. On neurological examination, she had normal mental status, muscle strength, gait, and cerebellar and sensory testing, including the face. There was no facial weakness and no weakness or atrophy of the tongue. On ophthalmological examination, she had anisocoria. The left pupil was dilated and did not respond to light stimulation, but slowly constricted with convergence (near response). Her visual acuity was 20/25 in the left eye and 20/20 in the right eye, uncorrected. She complained of severe pounding left frontal and orbital pain, but there was no exophthalmos or conjunctival inflammation. There was no ptosis. Extraocular movements were normal. On slit lamp exam, the corneas and lenses were clear. There was sectorial atrophy of the left iris with vermicular contractions. Her right eye examination was normal and her eye grounds showed normal retina and normal vessels and optic nerves. Her ocular pressure was 18 in the left eye and 12 in the right. Gold-