Riss J M, Girard N J, Proust H, Lebreuil G, Raybaud C A, Ridings B
Department of Ophthalmology, Hôpital Nord, Marseille, France.
Ophthalmologica. 1995;209(5):284-8. doi: 10.1159/000310633.
The authors examined the clinicopathologic features of a 4-year-old boy with a diffuse choroidal hemangioma, yet without any features of the Sturge-Weber syndrome. The tumor occurred as a grayish intraocular mass with an overlying retinal detachment and was highly reflective in the ultrasonic examination. After contrast, the CT scan revealed diffuse thickening of the ocular wall associated with an enhanced irregular orbital mass. The pathologic examination revealed a cavernous hemangioma involving the entire choroid with extrascleral extension. Diffuse choroidal hemangioma occurring in childhood and unrelated to the Sturge-Weber syndrome is a rare condition that should be included in the differential diagnosis of retinoblastoma.
作者检查了一名4岁患有弥漫性脉络膜血管瘤但无任何斯-韦综合征特征的男孩的临床病理特征。肿瘤表现为灰白色眼内肿块,伴有视网膜脱离,超声检查显示为高回声。增强扫描后,CT扫描显示眼壁弥漫性增厚,伴有不规则强化的眶内肿块。病理检查显示为海绵状血管瘤,累及整个脉络膜并向巩膜外扩展。儿童期发生且与斯-韦综合征无关的弥漫性脉络膜血管瘤是一种罕见疾病,应列入视网膜母细胞瘤的鉴别诊断。