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眼部幼年性黄色肉芽肿

Ocular juvenile xanthogranuloma.

作者信息

Niu Liangliang, Zhang Chaoran, Meng Fanrong, Cai Rongrong, Bi Yingwen, Wang Yan, Xu Jianjiang

机构信息

*MD †MD, PhD Departments of Ophthalmology (LN, CZ, FM, YW, JX) and Pathology (RC, YB), Eye and ENT Hospital of Fudan University, Shanghai, China.

出版信息

Optom Vis Sci. 2015 Jun;92(6):e126-33. doi: 10.1097/OPX.0000000000000609.

Abstract

PURPOSE

To report the clinical and histopathologic characteristics and prognoses of three ocular juvenile xanthogranuloma (JXG) cases.

CASE REPORTS

Three cases were included in this study. The first case involved a 5-year-old girl with an enlarging yellowish mass at the limbus with corneal involvement. Ultrasound biomicroscopy showed a poorly demarcated mass involving the underlying cornea and sclera. The mass was excised in combination with a lamellar keratoplasty procedure. No recurrence was seen at the 2-year follow-up. The second case involved a 2-year-old boy with an enlarging yellowish mass on the conjunctiva, without limbal involvement. The mass was excised with no recurrence noted 1 year later. The third case involved a 7-month-old girl with unilateral eye redness and photophobia combined with multiple orange-red, raised nodular lesions on the skin. Examination under general anesthesia revealed a gray-yellow mass in the inferior and temporal iridocorneal angles. The intraocular pressure and corneal diameter were normal. Examination using ultrasound biomicroscopy showed a high-level echo lump in the inferior and temporal angles. There was no treatment for this case. At the 1-year follow up, the eye symptoms had resolved and the skin lesions were flat. Histopathologic examinations were completed on all three cases. The presence of Touton giant cells in hematoxylin-eosin staining, positive CD68 staining, and negative S-100 and CD1a staining confirmed the diagnosis of JXG.

CONCLUSIONS

We report three histopathologically confirmed ocular JXG cases involving the corneoscleral limbus, conjunctiva, and iris with angle involvement, respectively. Ultrasound biomicroscopy performed on two cases demonstrated no obvious division between the mass and the surrounding structures. The cases with ocular surface involvement were successfully treated by excision and the case with iris involvement spontaneously regressed without any treatment. Early excision may be the better choice for ocular surface lesions, especially when corneal involvement is a possibility.

摘要

目的

报告3例眼部幼年性黄色肉芽肿(JXG)的临床、组织病理学特征及预后。

病例报告

本研究纳入3例病例。第1例为一名5岁女孩,角膜缘有一不断增大的淡黄色肿物,并累及角膜。超声生物显微镜检查显示肿物界限不清,累及下方角膜和巩膜。肿物切除并联合板层角膜移植术。2年随访未见复发。第2例为一名2岁男孩,结膜有一不断增大的淡黄色肿物,未累及角膜缘。肿物切除,1年后未见复发。第3例为一名7个月大的女孩,单眼眼红、畏光,皮肤有多个橙红色、隆起的结节性病变。全身麻醉下检查发现下方和颞侧虹膜角膜角有一灰黄色肿物。眼压和角膜直径正常。超声生物显微镜检查显示下方和颞侧房角有一高回声肿块。该病例未予治疗。1年随访时,眼部症状消失,皮肤病变变平。对所有3例病例均进行了组织病理学检查。苏木精-伊红染色可见杜顿巨细胞,CD68染色阳性,S-100和CD1a染色阴性,确诊为JXG。

结论

我们报告了3例经组织病理学证实的眼部JXG病例,分别累及角膜巩膜缘、结膜和伴有房角受累的虹膜。对2例进行的超声生物显微镜检查显示肿物与周围结构之间无明显分界。累及眼表的病例经切除成功治疗,累及虹膜的病例未经任何治疗自行消退。对于眼表病变,早期切除可能是更好的选择,尤其是当可能累及角膜时。

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