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Pulmonary granulomas in a patient with positive ANCA and history of tuberculosis: case report

BACKGROUND: Granulomatous polyangiitis (GPA) is a rare multisystem autoimmune disease of unknown aetiology that is pathologically characterised by necrotising vasculitis, tissue necrosis and granulomatous inflammation, typically in the presence of anti-neutrophil cytoplasmic antibodies (ANCA). Howev...

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Detalles Bibliográficos
Autores principales: Wong, B., Tan, E., McLean-Tooke, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427886/
https://www.ncbi.nlm.nih.gov/pubmed/32795275
http://dx.doi.org/10.1186/s12890-020-01258-9