| Literature DB >> 30297197 |
Silvia Suárez-Díaz1, Faustino Núñez-Batalla2, María Soledad Fernández-García3, María Belén Fernández-Llana4, Carmen Yllera-Gutiérrez5, Luis Caminal-Montero6.
Abstract
IgG4-related disease is characterized by a lymphoplasmacytic infiltrate rich in IgG4-positive plasma cells, storiform fibrosis and obliterative phlebitis. It can present as parotid gland enlargement, tubulointerstitial nephritis, retroperitoneal fibrosis or pancreatitis, although nearly any organ can be affected. We report the case of a 37-year-old woman who presented with severe dysphonia and recurrent painful aphthous ulcers, with histopathological findings at the level of the larynx that revealed a lymphoplasmacytic infiltrate and IgG4 positivity. In addition, extensive studies were performed to rule out other diseases. Thus the diagnosis was IgG4-related laryngitis, an exceptional finding in the literature.Entities:
Keywords: Aftosis oral; Aphthous stomatitis; Behçet's disease; Enfermedad de Behçet; Enfermedad relacionada con IgG4; IgG4-related disease; Laringitis; Laryngitis
Year: 2018 PMID: 30297197 DOI: 10.1016/j.reuma.2018.08.011
Source DB: PubMed Journal: Reumatol Clin (Engl Ed) ISSN: 2173-5743