Enfermedad relacionada a IgG4. Serie clínica de pacientes chilenos / IGG4-related disease. Report of 52 patients
Rev. med. Chile
; 150(6): 705-710, jun. 2022. tab, ilus
Article
em Es
| LILACS
| ID: biblio-1424121
Biblioteca responsável:
CL126.2
ABSTRACT
BACKGROUND:
IgG4-related disease (IgG4 RD) is an immune-mediated fibro-inflammatory disorder, with tissue infiltration of IgG4+ plasma cells. It causes pseudotumors, tumors, and a wide spectrum of clinical manifestations.AIM:
To report the clinical, laboratory, histopathological and treatment characteristics of a group of Chilean patients with IgG4 RD. MATERIAL ANDMETHODS:
Review of medical records of 52 patients aged 18 to 76 years with IgG4 RD seen at six medical centers.RESULTS:
Elevated IgG4 serum levels (> 135 mg/dl) were found in 18 of 44 (41%) patients. There was histological confirmation of the disease in 46 patients. The most common sites of involvement were lungs, eyes and kidneys. Eighteen (35%) patients had only one organ involved, 34 (65%) patients had two organs and 13 (25%) patients had three or more organs. The involvement of two organs was significantly more common in men (p < 0.05). In patients with only one organ involvement, the most frequent location was orbital and meningeal. All patients with kidney or lung disease had multiorgan involvement. All patients received corticosteroid therapy, 67% synthetic immunosuppressants, and 16% rituximab.CONCLUSIONS:
ER-IgG4 can affect any tissue. Multiorgan involvement was more common in this series, with preference for lungs, eyes and kidneys. An excellent response to steroids is characteristic of the disease, but with a high relapse rate that requires additional immunosuppression.Palavras-chave
Texto completo:
1
Base de dados:
LILACS
Assunto principal:
Doenças Autoimunes
/
Doença Relacionada a Imunoglobulina G4
País/Região como assunto:
America do sul
/
Chile
Idioma:
Es
Ano de publicação:
2022
Tipo de documento:
Article
País de afiliação:
Chile