Mocan Mehmet C, Bozkurt Banu, Orhan Diclehan, Kuzey Gamze, Irkec Murat
Department of Ophthalmology, Hacettepe University, School of Medicine, Ankara, Turkey.
Cornea. 2008 Jul;27(6):739-42. doi: 10.1097/QAI.0b013e31815c71f7.
To report the clinical and histopathologic findings of limbal juvenile xanthogranuloma lesions in 2 pediatric cases.
Case report and literature review.
Two cases (a 7-month-old girl and a 7-year-old boy), both of whom developed a yellowish corneoscleral limbal mass not associated with other ocular or systemic findings, were evaluated. Both cases underwent simple excision of the lesion followed by local steroid treatment. Histopathologic examination in both cases revealed foamy histiocytes within an inflammatory infiltrate. One of the lesions also harbored multinucleate giant cells. Immunohistochemical staining was positive for CD68 and negative for S-100 and CD1a in both cases.
Juvenile xanthogranuloma may rarely present with an isolated lesion occurring only at the corneoscleral limbus. The diagnosis in the early stages of this disorder may be established with immunophenotyping and characteristic histopathologic features even without the presence of the multinucleate giant cells.
报告2例儿童角膜缘幼年性黄色肉芽肿病变的临床和组织病理学表现。
病例报告及文献复习。
对2例患者(1例7个月大的女孩和1例7岁的男孩)进行了评估,二者均出现了黄白色角膜缘肿物,且无其他眼部或全身表现。2例均接受了病变的简单切除,随后进行局部类固醇治疗。2例的组织病理学检查均显示炎症浸润内有泡沫状组织细胞。其中1个病变还含有多核巨细胞。2例免疫组化染色CD68均为阳性,S-100和CD1a均为阴性。
幼年性黄色肉芽肿很少仅表现为孤立发生于角膜缘的病变。即使没有多核巨细胞,通过免疫表型分析和特征性组织病理学特征也可在该疾病的早期阶段做出诊断。