Abstract
Immunoglobulin G4-related sclerosing disease is a rare but potentially debilitating cause of orbital inflammation, with a predilection for older males. We report the case of a 12-year-old African girl with immunoglobulin G4-related sclerosing disease, including possible extraorbital involvement. Because of an escalating severity of illness leading to oculomotor nerve palsy and cavernous sinus thrombosis that was resistant to steroids, systemic immunosuppressive therapy with rituximab was used to achieve disease remission. The diagnosis was histologically confirmed with a tissue biopsy.
| Original language | English |
|---|---|
| Pages (from-to) | 548-550 |
| Number of pages | 3 |
| Journal | Journal of AAPOS |
| Volume | 17 |
| Issue number | 5 |
| DOIs | |
| State | Published - Oct 2013 |
| Externally published | Yes |