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Characteristics of ANCA-associated vasculitis with aneurysms: Case series and review of the literature.
Hankard, Antoine; Puéchal, Xavier; Martin Silva, Nicolas; Deshayes, Samuel; Lorcy, Nolwenn; Le Gallou, Thomas; Carron, Pierre-Louis; Daugas, Eric; Kaplanski, Gilles; Boutemy, Jonathan; Maigné, Gwénola; Galimard, Caroline; Terrier, Benjamin; Aouba, Achille; de Boysson, Hubert.
Afiliação
  • Hankard A; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France. Electronic address: antoine.hankard@inserm.fr.
  • Puéchal X; National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (APHP), Centre, Université Paris Cité, Paris, France.
  • Martin Silva N; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France.
  • Deshayes S; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France.
  • Lorcy N; Department of Nephrology, Rennes University Hospital, Rennes, France.
  • Le Gallou T; Department of Internal Medicine, Rennes University Hospital, South Hospital, Rennes, France.
  • Carron PL; Department of Nephrology, Grenoble University Hospital, Grenoble, France.
  • Daugas E; Department of Nephrology, Bichat-Claude-Bernard Hospital, University Hospital Center, APHP, Paris, France.
  • Kaplanski G; Department of Internal Medicine, La Conception Hospital, University Hospital Center, APHM, Marseille, France.
  • Boutemy J; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France.
  • Maigné G; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France.
  • Galimard C; Department of Infectious Disease Medicine, Caen University Hospital, Basse Normandie University, Caen, France.
  • Terrier B; National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (APHP), Centre, Université Paris Cité, Paris, France.
  • Aouba A; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France; Université de Caen Normandie, Caen, France.
  • de Boysson H; Department of Internal Medicine, Caen University Hospital, Basse Normandie University, Caen, France; Université de Caen Normandie, Caen, France.
Autoimmun Rev ; 22(5): 103293, 2023 May.
Article em En | MEDLINE | ID: mdl-36787809
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. Patients 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 aneurysmal 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article