Lim Zena, Quah Boon Long
Pediatric Ophthalmology and Strabismus Service, Singapore National Eye Centre, Singapore.
J AAPOS. 2010 Apr;14(2):184-6. doi: 10.1016/j.jaapos.2010.02.005.
Retinoblastoma and Peters anomaly are presumably unrelated ocular conditions, although other congenital ocular anomalies have been described in association with retinoblastoma. We report the case of a neonate who presented with unilateral retinoblastoma and Peters anomaly. Retinoblastoma arises from a deregulation of cellular events secondary to inactivation of both RB1 gene alleles, whereas Peters anomaly has been linked to eye-development genes and chromosomal anomalies. A second locus for retinoblastoma, RBL2, which encodes the p130 protein, has been shown to contribute to retinoblastoma oncogenesis. Coincidentally, p130 also plays a role in corneal cell differentiation. Although the association of retinoblastoma and Peters anomaly in this patient may be coincidental, it raises the question of whether the RBL2 mutation contributed to both conditions.
视网膜母细胞瘤和彼得斯异常可能是不相关的眼部疾病,尽管已有其他先天性眼部异常与视网膜母细胞瘤相关的描述。我们报告了一例患有单侧视网膜母细胞瘤和彼得斯异常的新生儿病例。视网膜母细胞瘤源于RB1基因两个等位基因失活继发的细胞事件失调,而彼得斯异常与眼部发育基因和染色体异常有关。视网膜母细胞瘤的第二个位点RBL2编码p130蛋白,已被证明与视网膜母细胞瘤的肿瘤发生有关。巧合的是,p130在角膜细胞分化中也起作用。尽管该患者视网膜母细胞瘤和彼得斯异常的关联可能是巧合,但它提出了一个问题,即RBL2突变是否导致了这两种情况。