Al-Zubidi Nagham, Oku Hidehiro, Verner-Cole Elizabeth, Chévez-Barrios Patricia, Tonari Masahiro, Kurimoto Takuji, Tsuji Motomu, Ikeda Tsunehiko, Lee Andrew G
Department of Ophthalmology, The Methodist Hospital Houston, TX USA.
Department of Ophthalmology, Osaka Medical College Osaka Japan.
Neuroophthalmology. 2013 Jan 29;37(1):24-30. doi: 10.3109/01658107.2012.752853. eCollection 2013.
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.
我们报告了两例经活检证实的免疫球蛋白G4相关性硬化性眼眶炎症(IgG4SOI)罕见病例。第一例有颅内受累情况,据我们所知,这是首例伴有血清脑脊液异常的IgG4SOI病例,第二例表现为压迫性视神经病变和全身淋巴结病的不寻常症状。