Cates Carolyn A, Dandekar Samantha S, Flanagan Declan W, Moore Anthony T
Department of Ophthalmology, Addenbrooke's Hospital, Cambridge, UK.
Ophthalmic Genet. 2003 Dec;24(4):247-52. doi: 10.1076/opge.24.4.247.17237.
A spectrum of retinal features has been recognised in association with incontinentia pigmenti. The majority of reported cases describe a rapidly progressive proliferative retinopathy, often leading to retinal detachment, emphasizing the potentially blinding nature of the disease. In some instances, the retinopathy has been noted to be less severe but follow-up has been short. We describe a young girl with incontinentia pigmenti in whom the retinopathy has shown a fluctuating but stable course over 13 years without treatment.
与色素失禁症相关的一系列视网膜特征已得到确认。大多数报告的病例描述为快速进展的增殖性视网膜病变,常导致视网膜脱离,突出了该疾病潜在的致盲性。在某些情况下,已注意到视网膜病变较轻,但随访时间较短。我们描述了一名患有色素失禁症的年轻女孩,其视网膜病变在未经治疗的情况下历经13年呈现出波动但稳定的病程。