Raja Muhammad, Goldsmith Craig, Burton Benjamin J L
Ophthalmology Department, James Paget University Hospital, NHS Foundation Trust, Great Yarmouth, Norfolk, UK.
BMJ Case Rep. 2011 Jul 27;2011:bcr0320113999. doi: 10.1136/bcr.03.2011.3999.
A 57-year-old woman, diagnosed with retinitis pigmentosa and positive family history, was referred to the retinal clinic. Full-thickness macular hole was noted in the right eye with no significant vitreomacular interface abnormalities confirmed at baseline visit with spectral-domain optical coherence tomography scan. Routine follow-up showed spontaneous closure of the full-thickness macular hole with four-letter improvement from baseline visit and remains unchanged with 3 years of follow-up.
一名57岁女性,被诊断患有色素性视网膜炎且有家族史阳性,被转诊至视网膜诊所。右眼发现全层黄斑裂孔,在基线检查时通过光谱域光学相干断层扫描未确认有明显的玻璃体黄斑界面异常。常规随访显示全层黄斑裂孔自发闭合,与基线检查相比视力提高了四行,且在3年的随访中保持不变。