医学
早产儿视网膜病变
视网膜病变
荧光血管造影
儿科
家族史
体格检查
基因检测
病史
视网膜
眼病
激光凝固
临床病史
外科
遗传咨询
突变
复合杂合度
眼科
既往病史
作者
Jacob Sperber,Sandra Hoyek,Celine Chaaya,Srujay Pandiri,Nimesh A. Patel,Jacob Sperber,Sandra Hoyek,Celine Chaaya,Nimesh A. Patel
标识
DOI:10.1177/24741264251393951
摘要
Purpose: To describe a rare case of late reactivation of retinopathy of prematurity (ROP) in a treatment-naive adult female patient. Methods: Clinical examination and multimodal imaging techniques were used to diagnose the patient and guide the treatment, and genetic saliva testing was performed. Results: We describe a 30-year-old female patient who presented with late reactivation of treatment-naive ROP. She was born prematurely and never received a diagnosis of ROP. She presented at the age of 30 years with new onset of flashes and floaters. Fundoscopic examination was consistent with a diagnosis of ROP, with peripheral avascularity evident in the temporal retina bilaterally, a temporal ridge in the right eye, and focal leakage seen bilaterally on fluorescein angiography. The patient was treated with panretinal photocoagulation laser therapy. Genetic testing demonstrated a heterozygous mutation in ZNF408 . Conclusions: Retinopathy associated with prematurity may reactivate in adulthood. This late reactivation may be influenced by a history of untreated ROP or by mutations associated with familial exudative vitreoretinopathy.
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