IgG4-related disease-rare but you should not forget it.

Autor: Pinheiro FAG; Rheumatology Division, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil. fredagp@hotmail.com.; Universidade Federal de São Paulo - Disciplina de Reumatologia, Rua Botucatu, 740, 3o andar, São Paulo, SP, 04023-062, Brazil. fredagp@hotmail.com., Pereira IA; Universidade do Sul de Santa Catarina (UNISUL), Florianopolis, SC, Brazil., de Souza AWS; Rheumatology Division, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil., Giardini HAM; Rheumatology Division, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, Brazil., Cordeiro RA; Rheumatology Division, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Jazyk: angličtina
Zdroj: Advances in rheumatology (London, England) [Adv Rheumatol] 2024 May 03; Vol. 64 (1), pp. 35. Date of Electronic Publication: 2024 May 03.
DOI: 10.1186/s42358-024-00374-y
Abstrakt: Immunoglobulin G4-related disease is a systemic immune-mediated disease with insidious evolution characterized by fibroinflammatory lesions over virtually any organ system. Despite the remarkable progression of knowledge, its etiology remains undefined. Due to its relapse-remitting pattern, it could accumulate irreversible damage, increasing comorbidities and mortality. This paper emphasizes key concepts for diagnosing and treating patients with this condition.
(© 2024. The Author(s).)
Databáze: MEDLINE
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