Bruner W E, Stark W J, Green W R
Arch Ophthalmol. 1982 Mar;100(3):457-9. doi: 10.1001/archopht.1982.01030030459016.
Juvenile xanthogranuloma (JXG) of the iris is extremely rare in adults. A case of presumed JXG occurred in a 26-year-old woman who was seen initially with bilateral iris lesions and spontaneous hyphema in one eye. Diagnosis was based on the clinical picture and the finding of typical histiocytes obtained by paracentesis and examined by a polymer filtration (Millipore) cytopathologic techniques. Treatment with steroids (given orally and topically to the eye) resulted in a substantial decrease in the size of the iris lesion of the left eye. She has received no medications for 18 months and has shown no signs of progression or other complications 24 months after the initial diagnosis.
虹膜幼年性黄色肉芽肿(JXG)在成年人中极为罕见。一名26岁女性被诊断为疑似JXG,她最初表现为双侧虹膜病变,其中一只眼睛出现自发性前房积血。诊断基于临床表现以及通过前房穿刺获取典型组织细胞并采用聚合物过滤(密理博)细胞病理学技术检查的结果。使用类固醇(口服及眼部局部给药)治疗后,左眼虹膜病变的大小显著减小。她在18个月内未服用任何药物,初诊后24个月未出现病情进展或其他并发症的迹象。