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先天性泪小点闭锁、泪囊瘘管合并鼻泪管闭锁临床罕见,国内外文献尚无报导。我们曾遇1例并进行治疗。报告如下。侯××,女,5岁,因自幼左眼溢泪、内眦下方小孔溢液于1989年11月3日就诊。眼科检查:右眼正常。左眼视力1.5,睑缘及上泪点无异常。下泪点缺如,仅在睑缘距内眦6.5mm 相当于下泪小点处见一不明显的小凹陷,较周围组织略显苍白,有新生血管
Congenital tear dot atresia, lacrimal sac fistula with nasolacrimal duct atresia clinical rare, there is no report at home and abroad. We have encountered 1 case and treated. The report is as follows. Hou × ×, female, 5 years old, due to childhood left eye overflowing, infiltration of small holes within the spit on November 3, 1989 treatment. Eye examination: right eye is normal. Left visual acuity 1.5, palpebral margin and on the tear point no exception. Under the tears point missing, only within the eyelid margin 内 6.5mm is equivalent to the next tear point to see an obvious small depression, slightly weaker than the surrounding tissue, with neovascular