| Literature DB >> 28163752 |
Nagham Al-Zubidi1, Hidehiro Oku2, Elizabeth Verner-Cole3, Patricia Chévez-Barrios4, Masahiro Tonari2, Takuji Kurimoto2, Motomu Tsuji5, Tsunehiko Ikeda2, Andrew G Lee6.
Abstract
We report two rare cases of biopsy proven Immunoglobulin G4-related sclerosing orbital inflammation (IgG4SOI). The first case had intracranial involvement which, to our knowledge, is the first IgG4SOI case with serum cerebrospinal fluid abnormalities and the second case had an unusual presentation of a compressive optic neuropathy and systemic lymphadenopathy.Entities:
Keywords: Compressive optic neuropathy; IgG4; immunoglobulin G4-positive sclerosing idiopathic orbital inflammation; immunoglobulin G4-positive with intracranial involvement; sclerosing idiopathic orbital inflammation; systemic lymphadenopathy
Year: 2013 PMID: 28163752 PMCID: PMC5289275 DOI: 10.3109/01658107.2012.752853
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107