Thromboangiitis obliterans with multiple large vessel involvement: case report and analysis of immunophenotypes

Abstract Thromboangiitis obliterans (TAO, Buerger's disease) is an idiopathic, recurrent, segmental, nonatherosclerotic, inflammatory, occlusive vascular disease with a poorly understood pathogenesis. Intestinal or multi-organ involvement is rare. Recent immunohistochemical analyses of ordinary...

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Veröffentlicht in:Cardiovascular pathology 2010, Vol.19 (1), p.59-62
Hauptverfasser: Edo, Naoki, Miyai, Kosuke, Ogata, Sho, Nakanishi, Kuniaki, Hiroi, Sadayuki, Tominaga, Susumu, Aiko, Satoshi, Kawai, Toshiaki
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Sprache:eng
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Zusammenfassung:Abstract Thromboangiitis obliterans (TAO, Buerger's disease) is an idiopathic, recurrent, segmental, nonatherosclerotic, inflammatory, occlusive vascular disease with a poorly understood pathogenesis. Intestinal or multi-organ involvement is rare. Recent immunohistochemical analyses of ordinary TAO have indicated an inflammatory and immunologic pathogenesis. We report a case of TAO involving multiple large vessels. By immunohistochemistry, CD3(+) T cells were revealed around the recanalization sites within the abdominal aorta. CD4(+) T cells were almost equal in number to CD8(+) T cells. These findings indicate the participation of inflammatory and immunologic processes in TAO with multi-organ involvement (as in ordinary TAO).
ISSN:1054-8807
1879-1336
DOI:10.1016/j.carpath.2008.10.004