Buerger's Disease in Two Brothers: Iliac Artery Occlusion by Thromboangiitis Obliterans

Author:

Wysokinski Waldemar E.1,Kwiatkowska Wieslawa1,Maslowski Leszek1,Witkiewicz Wojciech2,Kowal-Gierczak Barbara1

Affiliation:

1. Department and Clinic of Angiology, University Medical School of Wroclaw, County Specialistic Hospital of Wroclaw, Poland.

2. Department of General and Vascular Surgery, County Specialistic Hospital of Wroclaw, Poland.

Abstract

Several characteristics of thromboangiitis obliterans are unique and confirm the existence of the disease as a distinct pathological entity. Its predilection for young smoking males, peripheral type of vascular involvement, recurrences of superficial thrombophlebites, and typical histolopathology form the principals of the disease although the etiology remains unknown. The authors report the unusual finding of Buerger's disease occurring in two brothers, one of whom had occlusion of the left external iliac and femoral arteries. All other clinical characteristics of these two cases were typical for thromboangiitis oblit erans. Presentation of some peculiarities of the disease, particularly the lack of familial association, may help to unravel the pathogenesis of thromboangiitis obliterans.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

Reference22 articles.

1. Juergens JL: Thromboangiitis obliterans (Buerger's disease, TAO) In: Peripheral Vascular Diseases, ed. by Juergens JL, Spittell JA Jr, Fairbairn JF II. Philadelphia: WB Saunders Co, 1980, pp 467-491.

2. Buerger's Disease (Thromboangiitis Obliterans)

3. Autoimmunological aspects of thromboangiitis obliterans (Buerger's disease)

4. Cellular Sensitivity to Collagen in Thromboangiitis Obliterans

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