Methods: Ophtalmic examinations were made in 26 male patients with Buergers disease (mean age 40.4±9.6 years; range 22 to 56 years) who underwent lumbar sympathectomy, amputation, ulcer care and medical treatment and 26 healthy males (mean age 40.3±9.3 years; range 23 to 57 years) as a control group. There were no major atherosclerotic risk factors except for male gender and smoking.
Results: In the Buergers disease group, only two patients had normal fundus. There was mild optic atrophy in two patients. While grade I retinopathy was seen in 10 patients, and grade II retinopathy in 12 patients, only four individuals had grade I retinopathy (p<0.05) and the rest had normal fundus examinations in the control group.
Conclusion: In our study, atherosclerotic hypertensive grade I and II retinopathies were seen more frequently in Buergers disease group than control group although there were no major atherosclerotic risk factors, in both groups, like hypertension, hyperlipidemia, diabetes mellitus, and obesity except for smoking and male gender. This result shows that findings resembling hypertensive atherosclerotic retinopathy may develop in Buergers disease.
1) Shionoya S, Ban I, Nakata Y, Matsubara J, Hirai M, Kawai
S. Involvement of the iliac artery in Buergers disease
(pathogenesis and arterial reconstruction). J Cardiovasc Surg
1978;19:69-76.
2) Bozikas VP, Vlaikidis N, Petrikis P, Kourtis A, Karavatos
A. Schizophrenic-like symptoms in a patient with thromboangiitis
obliterans (Winiwarter-Buergers disease). Int J
Psychiatry Med 2001;31:341-6.
3) Donatelli F, Triggiani M, Nascimbene S, Basso C, Benussi S,
Chierchia SL, et al. Thromboangiitis obliterans of coronary
and internal thoracic arteries in a young woman. J Thorac
Cardiovasc Surg 1997;113:800-2.
4) Deitch EA, Sikkema WW. Intestinal manifestation of
Buergers disease: case report and literature review. Am Surg
1981;47:326-8.
5) Olin JW, Shih A. Thromboangiitis obliterans (Buergers
disease). Curr Opin Rheumatol 2006;18:18-24.
6) Olin JW. Thromboangiitis obliterans (Buergers disease).
In: Rutherford RB, editor. Vascular surgery. 6th ed. Vol. 1,
Philadelphia: W. B. Saunders; 2005. p. 404-19.
7) Bozkurt AK, Beşirli K, Köksal C, Sirin G, Yüceyar L, Tüzün
H, et al. Surgical treatment of Buergers disease. Vascular
2004;12:192-7.
8) Ohguro I, Ohguro H, Ohta T, Nakazawa M. A case of normal
tension glaucoma associated with Buergers disease. Tohoku
J Exp Med 2006;209:49-52.
9) Puttanna ST. Thromboangeitis associated with retinal vasculitis.
J All India Ophthalmol Soc 1966;14:209-13.
10) Shionoya S. Buergers disease (thromboangiitis obliterans).
In: Rutherford RB, editor. Vascular surgery. 3rd ed.
Philadelphia: W. B. Saunders; 1989. p. 207-17.
11) Lie JT. Diagnostic histopathology of major systemic and
pulmonary vasculitic syndromes. Rheum Dis Clin North Am
1990;16:269-92.
12) Olin JW. Thromboangiitis obliterans (Buergers disease). N
Engl J Med 2000;343:864-9.
13) Olin JW, Young JR, Graor RA, Ruschhaupt WF, Bartholomew
JR. The changing clinical spectrum of thromboangiitis
obliterans (Buergers disease). Circulation 1990;82(5
Suppl):IV3-8.
14) Flammer J, Pache M, Resink T. Vasospasm, its role in the
pathogenesis of diseases with particular reference to the eye.
Prog Retin Eye Res 2001;20:319-49.