Background: Ocular involvement in panarteritis nodosa (PAN) has been report
ed to occur in 10 to 20% of patients. In 3 patients with acute Visual distu
rbance we point out unusual findings.
Patients: Case 1. A 40-year-old man initially presented with papilledema to
gether with partial optic atrophy in both eyes, rater polyneuropathy, gangr
ene of the toes and myalgic pains developed. Caliber changes in the small a
rteries in the liver were seen angiographically and recognized as signs of
PAN. Under treatment with cyclophosphamide und prednisone no relapse occurr
ed during a follow-up of 2 years. Case 2. in a 67-year-old man who suffered
from arterial hypertension and coronary heart disease, central retinal art
ery occlusion occurred, at first in the left and then later in the right ey
e. The clinically suspected diagnosis of PAN (arterial hypertension, myalgi
a, polyneuropathy) was confirmed by a muscle biopsy. During a follow-up of
4 years - including treatment with prednisone and cyclophosphamide - no rel
apse occurred. Case 3. A 16-year-old adolescent with throbbing headaches an
d a thickened right temporal artery reported Visual disturbances. These wer
e due to an inflammation of choroidal vessels of the right eye appearing as
an initial sign of PAN. Histology revealed a necrotising arteritis of the
temporal artery. He presented with signs of Raynaud's disease, cachexia and
arterial hypertension. Multiple vasculitic changes were detected by aorto-
arteriography. Five months after the visual deterioration an anterior spina
l artery syndrome with quadriplegia developed. After a follow-up of 2 years
and treatment with prednisone und cyclophosphamide, he still had paralysis
of both legs. The Visual acuity was 1.0 in each eye.
Conclusion: PAN should be considered in differential diagnosis in patients
with acute inflammatory signs of the optic nerve head, the choroid and/or t
he retina together with general signs of the disease. If the disease is sus
pected, a muscle biopsy is indicated.