@Article{Dylewska2020,
journal="Postępy w chirurgii głowy i\ szyi/Advances in Head and Neck Surgery",
issn="1643-9279",
volume="19",
number="1",
year="2020",
title="Tumor of the orbit and pterygopalatine fossa as a manifestation of IgG4-related disease",
abstract="IgG4-related disease (IgG4-RD) is a systemic fibrotic-inflammatory disease characterized by elevated serum concentration of IgG4 and infiltration of tissues by plasma cells. IgG4-RD may occur as an isolated disease or co-exist with other inflammatory conditions, such as Mikulicz’s disease, autoimmune pancreatitis, sinusitis, thyroiditis, interstitial pneumonitis, nephritis, lymphadenopathy, inflammatory pseudotumor. IgG4-RD is a separate, clinically distinct disease entity, but due to its heterogeneous manifestation raises the interest of physicians with various specialties. The gold standard in the diagnosis is a histopathological examination.",
author="Dylewska, Katarzyna
and Kobusińska, Katarzyna
and Kurylak, Andrzej",
pages="4--7",
url="https://www.termedia.pl/Tumor-of-the-orbit-and-pterygopalatine-fossa-as-a-manifestation-of-IgG4-related-disease,11,42637,1,1.html"
}