Al-Ghadeer Huda, Al-Rajhi Ali, Riley Fenwick
Anterior Segment Division, King Khaled Eye Specialist Hospital, Riyadh - Kingdom of Saudi Arabia.
Eur J Ophthalmol. 2009 Mar-Apr;19(2):292-4. doi: 10.1177/112067210901900220.
To report on a case of episcleral hemangioma in a child.
A 3-year-old boy presented with a 4-week history of limbal mass in the left eye and had an excision of that mass.
There was an 8 x 7 mm oval lesion, 3-4 mm below the inferior limbus. It was reddish, sharply elevated with smooth surface, and firmly attached to the underlying sclera with two large blood vessels over it. Histopathologic examination demonstrated a cellular lesion containing vascular spaces of various sizes. The solid appearance indicated an increase of cells that appear to be consistent with endothelial cells which formed a nest surrounded by PAS-positive strands. Small to moderate size capillaries were evident throughout the solid portion of the lesion. These findings were consistent with episcleral hemangioma of capillary type.
Episcleral hemangioma is a rare tumor and should be included in the differential diagnosis of episcleral tumors. To our knowledge, this is the first reported case of episcleral hemangioma in a child as an isolated finding.
报告一例儿童巩膜上血管瘤病例。
一名3岁男孩因左眼角膜缘肿物4周就诊,对该肿物进行了切除。
在下方角膜缘下方3 - 4毫米处有一个8×7毫米的椭圆形病变。病变呈红色,明显隆起,表面光滑,牢固附着于下方巩膜,上方有两条大血管。组织病理学检查显示为一个细胞性病变,含有各种大小的血管腔隙。实性外观表明细胞增多,这些细胞似乎与内皮细胞一致,形成了一个被PAS阳性条索包围的巢。在病变的实性部分可见小到中等大小的毛细血管。这些发现符合毛细血管型巩膜上血管瘤。
巩膜上血管瘤是一种罕见肿瘤,应列入巩膜肿瘤的鉴别诊断。据我们所知,这是首例作为孤立发现报告的儿童巩膜上血管瘤病例。