Saraux H, Laroche L, Josset P, Fourre C
J Fr Ophtalmol. 1985;8(8-9):579-84.
Three cases of orbito-palpebral lymphangioma are reported. The three cases all have the common features: onset in early childhood, slow progression and extension of the tumor to other structures (palate and temporal fossa). The usual complications (hemorrhage and cellulitis) were documented in our cases. Biopsy of the lesions showed variably sized endothelial lined spaces without a capsule. Theses spaces contain eosinophilic material without blood elements. In two cases, chirurgical excision gave orbital edema. The authors think that orbital lymphangioma is a clinical entity. The treatment is difficult and small repeated excisions and cryotherapy are recommended.
报告了3例眶睑淋巴管瘤。这3例均具有共同特征：发病于儿童早期，肿瘤进展缓慢并蔓延至其他结构（腭部和颞窝）。我们的病例记录了常见并发症（出血和蜂窝织炎）。病变活检显示大小不一的内皮衬里腔隙，无包膜。这些腔隙含有嗜酸性物质，无血液成分。2例手术切除后出现眼眶水肿。作者认为眼眶淋巴管瘤是一种临床实体。治疗困难，建议进行小范围重复切除和冷冻治疗。
