| Literature DB >> 33517484 |
Francisca Guimarães1, Daniela Santos-Faria2, Soraia Azevedo2, Joana Ramos Rodrigues2, Joana Leite Silva2, Diogo Esperança-Almeida3, Bárbara Ribeiro4, Raquel Vaz4, Filipa Teixeira2, José Tavares-Costa2, Carmo Afonso2, Daniela Peixoto2.
Abstract
Coexistence of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and inflammatory bowel disease (IBD) is rare (Sy et al. in Semin Arthritis Rheum 45:475-482, 2016). Nevertheless, we present a case of an AAV in a 53-year-old female with enteropathic spondylarthritis previously treated with tumor necrosis factor α inhibitors (TNFi). Management of vasculitis in a patient with IBD may be problematic due to the difficulty in distinguishing if the vasculitis is an extraintestinal manifestation of the IBD or a new coexistent entity. Moreover, in our report, the previous treatment with TNFi is a possible confounding factor due to the paradoxical effects induced by TNFi, including vasculitis (Ramos-Casals et al. in Curr Rheumatol Rep 10:442-448, 2008). The reported case alerts to the complexity in the management of patients with enteropathic spondylarthritis and vasculitis, as well as discusses the diversity of differential diagnosis in this particular clinical scenario.Entities:
Keywords: ANCA vasculitis; Enteropathic spondylarthritis; Granulomatosis with polyangiitis; Inflammatory bowel disease
Year: 2021 PMID: 33517484 DOI: 10.1007/s10067-021-05612-y
Source DB: PubMed Journal: Clin Rheumatol ISSN: 0770-3198 Impact factor: 2.980