| Literature DB >> 19840735 |
Fernandino A Fontanilla1, Deepak P Edward, Margaret Wong, Howard H Tessler, Ralph C Eagle, Debra A Goldstein.
Abstract
Juvenile xanthogranuloma (JXG) of the uvea is a rare disease that usually responds to systemic steroids or low-dose radiotherapy. We present an atypical case of bilateral JXG involving the entire uveal tract that presented with an aggressive phenotype. The patient was unresponsive to topical and systemic corticosteroids, cyclosporine, and maximal doses of radiation therapy. The disease was ultimately controlled with the alkylating agent chlorambucil.Entities:
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Year: 2009 PMID: 19840735 DOI: 10.1016/j.jaapos.2009.06.010
Source DB: PubMed Journal: J AAPOS ISSN: 1091-8531 Impact factor: 1.220