Singh Arun D, Raval Vishal, Bellerive Claudine, Gopinath Bamini, Liew Gerald, Mitchell Paul
Ophthalmic Oncology, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
Ophthalmic Oncology, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
J AAPOS. 2021 Dec;25(6):327.e1-327.e5. doi: 10.1016/j.jaapos.2021.07.009. Epub 2021 Oct 30.
To investigate prevalence and age of onset of choroidal melanocytic lesions (other than nevi) in pediatric patients.
The pooled data of participants 6 months to 18 years of age in the Sydney Paediatric Eye Disease Study, the Sydney Myopia Study, and the Sydney Adolescent Vascular Eye Disease Study were reviewed retrospectively to identify children with choroidal melanocytic lesions. The clinical features and prevalence by age were assessed.
From the pooled sample of 5,533 unique children, 39 cases of focal melanocytic aggregates and 22 cases of choroidal melanocytosis were identified, with overall prevalence of 0.70% and 0.40%, respectively. There was a statistically significant trend toward increased prevalence with increasing age. Both focal melanocytic aggregates and choroidal melanocytosis tended to be bilateral (100% and 86% respectively), brown in color, and temporally located in all cases. Amelanotic variants were not identified. Focal melanocytic aggregates were small (0.15-0.5 mm), whereas choroidal melanocytosis varied in size (5.0-20 mm). All focal melanocytic aggregates were characteristically located 4-5 mm temporal to the center of the fovea and were associated with linear nervelike (11 [28%]) or tortuous vessel like structures (10 [26%]).
In this study, pooled data from large population studies revealed morphologic patterns of choroidal melanocytic lesions, other than nevus, that correlate with described clinical appearance in adults. The association of focal melanocytic aggregates with nervelike structures supports their embryologic origin along the migration path of uveal melanocytes.
研究儿科患者脉络膜黑素细胞病变(痣除外)的患病率及发病年龄。
回顾性分析悉尼儿童眼病研究、悉尼近视研究和悉尼青少年血管性眼病研究中6个月至18岁参与者的汇总数据,以确定患有脉络膜黑素细胞病变的儿童。评估其临床特征和按年龄划分的患病率。
在5533名儿童的汇总样本中,共识别出39例局灶性黑素细胞聚集和22例脉络膜黑素沉着症,总体患病率分别为0.70%和0.40%。随着年龄增长,患病率有统计学意义的上升趋势。局灶性黑素细胞聚集和脉络膜黑素沉着症均倾向于双侧(分别为100%和86%),颜色为棕色,且均位于颞侧。未发现无色素变体。局灶性黑素细胞聚集较小(0.15 - 0.5毫米),而脉络膜黑素沉着症大小不一(5.0 - 20毫米)。所有局灶性黑素细胞聚集均特征性地位于黄斑中心颞侧4 - 5毫米处,并与线性神经样结构(11例[28%])或迂曲血管样结构(10例[26%])相关。
在本研究中,来自大型人群研究的汇总数据揭示了痣以外的脉络膜黑素细胞病变的形态学模式,这与成人中描述的临床表现相关。局灶性黑素细胞聚集与神经样结构的关联支持了它们沿葡萄膜黑素细胞迁移路径的胚胎学起源。