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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container_end_page 62
container_issue 1
container_start_page 59
container_title Cardiovascular pathology
container_volume 19
creator Edo, Naoki
Miyai, Kosuke
Ogata, Sho
Nakanishi, Kuniaki
Hiroi, Sadayuki
Tominaga, Susumu
Aiko, Satoshi
Kawai, Toshiaki
description 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).
doi_str_mv 10.1016/j.carpath.2008.10.004
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subjects Fatal Outcome
Humans
Immunohistochemistry
Immunophenotype
Immunophenotyping
Intestinal Buerger's disease
Male
Middle Aged
Pathology
Smoking
T-Lymphocyte Subsets - immunology
Thromboangiitis obliterans
Thromboangiitis Obliterans - immunology
Thromboangiitis Obliterans - pathology
Thromboangiitis Obliterans - physiopathology
title Thromboangiitis obliterans with multiple large vessel involvement: case report and analysis of immunophenotypes
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