Characteristics of ANCA-associated vasculitis with aneurysms: Case series and review of the literature

被引:6
作者
Hankard, Antoine [1 ]
Puechal, Xavier [2 ]
Silva, Nicolas Martin [1 ]
Deshayes, Samuel [1 ]
Lorcy, Nolwenn [3 ]
Le Gallou, Thomas [4 ]
Carron, Pierre-Louis [5 ]
Daugas, Eric [6 ]
Kaplanski, Gilles [7 ]
Boutemy, Jonathan [1 ]
Maigne, Gwenola [1 ]
Galimard, Caroline [8 ]
Terrier, Benjamin [2 ]
Aouba, Achille [1 ,9 ]
de Boysson, Hubert [1 ,9 ]
机构
[1] Basse Normandie Univ, Caen Univ Hosp, Dept Internal Med, Caen, France
[2] Univ Paris Cite, Hop Cochin, Assistance Publ Hop Paris APHP, Natl Referral Ctr Rare Syst Autoimmune Dis,Ctr, Paris, France
[3] Rennes Univ Hosp, Dept Nephrol, Rennes, France
[4] Rennes Univ Hosp, South Hosp, Dept Internal Med, Rennes, France
[5] Grenoble Univ Hosp, Dept Nephrol, Grenoble, France
[6] Bichat Claude Bernard Hosp, APHP, Dept Nephrol, Univ Hosp Ctr, Paris, France
[7] La Concept Hosp, APHM, Dept Internal Med, Univ Hosp Ctr, Marseille, France
[8] Basse Normandie Univ, Caen Univ Hosp, Dept Infect Dis Med, Caen, France
[9] Univ Caen Normandie, Caen, France
关键词
ANCA-associated vasculitis; Aneurysms; Aneurysmal rupture; Granulomatosis with polyangiitis; RHEUMATOLOGY CLASSIFICATION CRITERIA; 2022; AMERICAN-COLLEGE; MICROSCOPIC POLYANGIITIS; POLYARTERITIS-NODOSA; ALPHA-1-ANTITRYPSIN DEFICIENCY; GRANULOMATOSIS; ALLIANCE; AZATHIOPRINE; MAINTENANCE; INVOLVEMENT;
D O I
10.1016/j.autrev.2023.103293
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: ANCA-associated vasculitis (AAV) is an exceptional cause of small and large vascular aneurysms. Here, we present the phenotypic characteristics of patients with AAV associated with the presence of aneurysms.Methods: We conducted a retrospective multicenter study and a systematic review of the literature. Only AAV patients with positive ANCA results and > 1 aneurysm(s) were enrolled. Patients were recruited through a call of observations among the French Vasculitis Study Group (FVSG) and the French Internal Medicine Network. Pa-tients with aneurysm rupture were compared to those without.Results: We enrolled 51 patients in the cohort, including 31 (67%) with granulomatosis with polyangiitis. The median Birmingham Vasculitis Activity Score was 18 [6-41]. A total of 92 aneurysms were noted, 74% of which involved medium-sized arteries, particularly the renal artery. During a follow-up of 24 [6-56] months, 22 (43%) patients experienced aneurysmal rupture, 91% of which involved medium-sized vessels. Patients with aneu-rysmal rupture showed significantly more pulmonary infiltrates and higher creatinine levels at baseline than patients without rupture. Initial treatments did not differ between the two groups. Ten (20%) patients died during the follow-up, including three from an aneurysmal rupture.Conclusion: Aneurysms were more frequently observed in GPA patients and predominantly affected medium-sized vessels, especially the renal arteries. The risk of rupture was high and occurred in >40% of patients. Because of their increased mortality, further studies are required to better manage this subset of patients.
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页数:7
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