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Fulminant alveolar hemorrhage: Evolution of giant cell arteritis to ANCA-positive vasculitis?
被引:5
|作者:
Garrouste, C.
[1
]
Sailler, L.
[1
]
Astudillo, L.
[1
]
Lavaysseire, L.
[2
]
Cointault, O.
[2
]
Borel, C.
[1
]
Bernard, J.
[3
]
Arlet, P.
[1
]
机构:
[1] CHU Toulouse, Hop Purpan, Serv Med Interne, F-31059 Toulouse, France
[2] CHU Toulouse, Serv Nephrol, Hop Rangueil, F-31059 Toulouse, France
[3] CHU Toulouse, Serv Rhumatol, Hop Rangueil, F-31059 Toulouse, France
来源:
关键词:
giant cell arteritis;
temporal arteritis;
Alveolar hemorrhage;
Wegener's granulomatosis;
ANCA;
D O I:
10.1016/j.revmed.2007.08.012
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Introduction. - Giant cell arteritis (GCA) is a granulomatous vasculitis of the large and medium size vessels with a remarkable sensitivity to corticosteroids. although it may be dependent to therapy. In rare cases, a vasculitis of the medium or small-size vessels may mimic, be associated to, or follow GCA. We report a case of GCA dependent to corticosteroids that was followed five, ears after diagnosis by an alveolar hemorrhage leading to the diagnosis of a possible Wegener's granulomatosis. Exegesis. - A 70-year-old man had a diagnosis of GCA fulfilling the ACR criteria in 1999. Temporal artery biopsy revealed a typical histological pattern. The initial response to corticosteroids was excellent, but the patient became dependent to corticosteroids, so he was given methotrexate from 2002. Severe alveolar haemorrhage occurred in December 2004, leading to the diagnosis of possible ANCA positive, anti-proteinase 3 positive Wegener's granulomatosis. Conclusion. - ANCA-positive vasculitis may complicate the course of GCA. This evolution should be rapidly recognized, because its treatment differs to that of GCA. (C) 2007 Elsevier Masson SAS. Tous droits reserves.
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页码:232 / 235
页数:4
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