- Letter to the Editor
- Open Access
Vogt–Koyanagi–Harada disease: headache as an initial manifestation
© Springer-Verlag 2008
- Received: 29 March 2008
- Accepted: 12 May 2008
- Published: 30 May 2008
- Optic Disk
- Intracranial Hypertension
- Optic Neuritis
- Pituitary Apoplexy
Vogt–Koyanagi–Harada (VKH) disease is a granulamatous inflammatory disease affecting the eyes, auditory system, meninges and the skin . Although headache, a prodromal sign, is present in 67% of patients , VKH disease is rarely encountered in neurology practice [3, 4].
Case 2 A 47-year-old woman presented with a 3-week history of diffuse and bilateral, orbito-retroorbital headache and bilateral acute vision loss. Cranial CT, MRI and MR angiography were normal. CSF pressure was normal. Analysis of CSF revealed 90% of monocytosis. Her funduscopic examination showed hyperemia and swelling of the optic disk. She was diagnosed with incomplete VKH. For ten days, 1 g/kg IVMP treatment was administered. In the sixth day of the treatment headache and visual complaints were improved. Treatment continued with high dose oral steroid (2 mg/kg) and decreased gradually.
In patients with VKH disease meningeal involvement may cause severe devastating headache mimicking other types of acute headaches. Symptoms might be interpreted as optic neuritis, pituitary apoplexy or intracranial hypertension if headache is associated with ocular findings. Moreover, integumentary symptoms such as allopesia, poliosis, vitiligo appear only late at the convalescent stage of the disease. Therefore, the diagnostic criteria lack sensitivity for the early diagnosis of VKH disease particularly in neurology emergencies. If the brain MRI is normal, diagnosis could be more confusing. VKH disease should be considered in the differential diagnosis of patients presenting with acute headache followed by bilateral blurred vision. Early diagnosis and adequate treatment are the keys to success. Corticosteroid is essential in the management of VKH disease.
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