Sommer F, Pillunat L E
Klinik und Poliklinik für Augenheilkunde, Medizinische Fakultät der Technischen Universität Dresden.
Klin Monbl Augenheilkd. 2004 Oct;221(10):872-7. doi: 10.1055/s-2004-813599.
In a strict sense epibulbar dermoids are defined as congenital changes of mesodermal and ectodermal origin. Usually they are located at the limbus of the cornea in the inferotemporal quadrant, they can only rarely be observed in more central regions of the cornea. Intraocular structures are rarely involved. Connections to Goldenhar's oculo-auriculo-syndrome exist. Because of cosmetic reasons or a considerable astigmatism holding the danger of amblyopia a resection might be necessary.
Six patients (three girls and three boys) aged from 9 months to 6 years with limbal dermoids were included in the present study. All patients had been referred to the University Eye Hospital of Dresden for a possible therapy.
All children showed a unilateral dermoid in the inferotemporal quadrant. In five cases the left eye was affected. In two patients a Goldenhar syndrome was present. In two patients a local resection of the dermoid was indicated. In three patients a keratoplasty (two lamellar, one penetrating) was additionally carried out. In the case of a two-year-old girl only prophylactic treatment of amblyopia was considered. The postoperative results reached from uncomplicated healing (visual acuity 1.0) to full cloudiness of the transplant and re-keratoplasty (visual acuity lux).
Controls of the dermoid in half-year intervals and surgical intervention in early childhood are recommended. Simple local resection or a combination with lamellar or penetrating (sclero)-keratoplasty are used. A penetrating keratoplasty is seldom necessary due to deep and central dermoids. The prognosis can be described as favourable.
严格意义上讲,眼球表面皮样瘤被定义为中胚层和外胚层起源的先天性病变。通常它们位于角膜缘的颞下象限,极少能在角膜更中央的区域观察到。眼内结构很少受累。与Goldenhar眼耳综合征存在关联。出于美容原因或存在导致弱视风险的明显散光,可能需要进行切除手术。
本研究纳入了6例年龄从9个月至6岁的患有角膜缘皮样瘤的患者(3名女孩和3名男孩)。所有患者均因可能需要治疗而被转诊至德累斯顿大学眼科医院。
所有儿童均表现为颞下象限的单侧皮样瘤。5例患者左眼受累。2例患者存在Goldenhar综合征。2例患者需要对皮样瘤进行局部切除。3例患者还额外进行了角膜移植术(2例板层角膜移植术,1例穿透性角膜移植术)。对于一名两岁女孩,仅考虑了弱视的预防性治疗。术后结果从无并发症愈合(视力1.0)到移植片完全混浊及再次角膜移植术(视力为光感)不等。
建议每半年对皮样瘤进行一次检查,并在儿童早期进行手术干预。采用简单的局部切除或与板层或穿透性(巩膜)角膜移植术联合使用。由于皮样瘤位置深且位于中央,很少需要进行穿透性角膜移植术。预后可描述为良好。