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IgG4-related disease presenting as posterior scleritis and vitritis, progressing to multifocal orbital involvement
IgG4-related disease (IgG4-RD) is a rare, chronic inflammatory condition that may involve nearly every organ system. Originally identified as a cause of autoimmune pancreatitis, its characteristic histological and clinical features have been found in a wide variety of inflammatory presentations, inc...
Gorde:
| Argitaratua izan da: | BMJ Case Rep |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMJ Case Reports
2017
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5534934/ https://ncbi.nlm.nih.gov/pubmed/28438752 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2017-219568 |
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