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角膜缘青少年黄色肉芽肿:两例报告

Juvenile xanthogranuloma of the corneoscleral limbus: report of two cases.

作者信息

De Keyser Christophe, Maudgal Prabhat, Legius Eric, Van Ginderdeuren Rita, Casteels Ingele

机构信息

Department of Ophthalmology, University Hospitals, Leuven, Belgium.

出版信息

Ophthalmic Genet. 2011 Mar;32(1):54-6. doi: 10.3109/13816810.2010.535888. Epub 2010 Dec 21.

Abstract

PURPOSE

To report the clinical and histopathologic findings of limbal juvenile xanthogranuloma (JXG) in two children.

METHODS

Case report.

RESULTS

Two children (a 9-month old boy and a 4-year old girl) presented with an enlarging yellowish mass at the corneoscleral limbus. The girl had been diagnosed with neurofibromatosis 1 (NF1). Both lesions underwent simple excision. Histopathologic examination revealed foamy histiocytes within an inflammatory infiltrate with the presence of multiple multinucleated giant cells. In both cases intraoperative subconjunctival steroids and postoperative topical steroids were administered during 1 month.

CONCLUSIONS

Juvenile xanthogranuloma may rarely present as a mass occurring at the corneoscleral limbus. Therefore it should be considered in the differential diagnosis of any corneoscleral limbal mass lesion, particularly in children. Most are isolated lesions without systemic involvement which are treated by simple excision. But association with NF1 is possible and in that case screening for hematological malignancies is recommended.

摘要

目的

报告两例儿童角膜缘幼年性黄色肉芽肿(JXG)的临床和组织病理学表现。

方法

病例报告。

结果

两名儿童(一名9个月大的男孩和一名4岁的女孩)在角膜缘处出现一个不断增大的淡黄色肿块。该女孩被诊断为1型神经纤维瘤病(NF1)。两个病变均接受了单纯切除术。组织病理学检查显示在炎性浸润内有泡沫状组织细胞,并存在多个多核巨细胞。在这两个病例中,术中均给予结膜下类固醇药物,术后局部使用类固醇药物1个月。

结论

幼年性黄色肉芽肿很少表现为发生在角膜缘的肿块。因此,在任何角膜缘肿块病变的鉴别诊断中都应考虑到它,尤其是在儿童中。大多数是孤立性病变,无全身受累,通过单纯切除进行治疗。但可能与NF1相关,在这种情况下,建议筛查血液系统恶性肿瘤。

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