Fontanilla Fernandino A, Edward Deepak P, Wong Margaret, Tessler Howard H, Eagle Ralph C, Goldstein Debra A
Department of Ophthalmology, University of Illinois at Chicago, Eye Infirmary, USA.
J AAPOS. 2009 Oct;13(5):515-8. doi: 10.1016/j.jaapos.2009.06.010.
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.
葡萄膜青少年黄色肉芽肿(JXG)是一种罕见疾病,通常对全身用类固醇或低剂量放疗有反应。我们报告一例累及整个葡萄膜的双侧JXG非典型病例,该病例表现出侵袭性表型。该患者对局部和全身用皮质类固醇、环孢素及最大剂量放疗均无反应。该疾病最终通过烷化剂苯丁酸氮芥得到控制。