Granulomatosis with polyangiitis – the incomplete puzzle
Authors
Ana Catarina Duarte; Ana Cordeiro; Pedro Gonçalves; Maria José Santos;
Granulomatous with polyangiitis (GPA) is a necrotizing granulomatous vasculitis that mostly affects small-sized vessels. The disease can affect many organs, although renal and respiratory tract involvement are the most frequent and distinguishing features. Musculoskeletal manifestations have been reported in about 50% of patients and can occur as myalgia, oligoarthralgia/arthritis of large joints or polyarthralgia/arthritis of small joints. Infrequently musculoskeletal symptoms can be the first disease manifestation, and in this clinical scenario GPA diagnosis might be delayed or mistaken by other rheumatic diseases. The authors describe three patients with musculoskeletal symptoms as earliest GPA manifestations, illustrating the clinical challenge.
Ana Catarina Duarte
Serviço de Reumatologia, Hospital Garcia de Orta
Ana Cordeiro
Serviço de Reumatologia, Hospital Garcia de Orta
Pedro Gonçalves
Serviço de Reumatologia, Hospital Garcia de Orta
Maria José Santos
Serviço de Reumatologia, Hospital Garcia de Orta; Instituto de Investigação em Reumatologia, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa
Serviço de Reumatologia, Hospital Garcia de Orta
Ana Cordeiro
Serviço de Reumatologia, Hospital Garcia de Orta
Pedro Gonçalves
Serviço de Reumatologia, Hospital Garcia de Orta
Maria José Santos
Serviço de Reumatologia, Hospital Garcia de Orta; Instituto de Investigação em Reumatologia, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa