孤立的单侧晶状体颞部疣

S. Suman, Arushi Kumar, H. U. Rathod
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摘要

晶状体角膜瘤是一种罕见的先天性畸形,是由于胎儿的裂隙未能完全闭合而导致晶状体形成不完全,因此通常是下鼻孔。颞叶晶状体瘤极为罕见,已报道的病例均伴有眼部或全身异常。我们报告了一例罕见的单侧非典型颞晶状体巨乳头瘤病例,患者没有任何虹膜异常、后节巨乳头瘤或其他眼部或全身异常。一名 18 岁女性患者的左眼视力逐渐减退,且无疼痛感,已持续两年。无外伤史,无家族史。全身检查正常。眼部检查显示,右眼视力为 6/6,左眼视力为 6/60,散瞳后左眼视力改善为 6/24,左眼晶状体有针孔和单侧非典型颞部胶质瘤。其他前段和眼底检查均正常。右眼未发现异常。随访 6 个月后,经眼镜矫正,患者的最佳矫正视力为 6/6 OD 和 6/9 OS。本病例是一例罕见的位于颞侧的单侧非典型麦粒肿,没有任何虹膜异常、后节麦粒肿或任何其他眼部或全身异常。早期矫正屈光不正和散光可获得良好的预后。
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Isolated Unilateral Temporal Coloboma of the Lens
Lens coloboma is a rare congenital anomaly that occurs due to failure of the foetal fissure to close completely causing an incomplete formation of the lens, so usually inferonasal. Temporal lens coloboma is extremely rare; reported cases were associated with ocular or systemic anomalies. We report a rare case of unilateral atypical temporal lens coloboma without any iris abnormality and posterior segment coloboma or any other ocular or systemic anomaly. An 18-year-old female presented with a gradually progressive painless diminution of vision in her left eye for two years. There was no history of trauma, and family history was non-contributory. The systemic examination was normal. Ocular examination revealed a vision of 6/6 in the right eye and 6/60 in the left eye improving to 6/24 with pinhole and unilateral atypical temporal coloboma of the crystalline lens in the left eye after dilatation. The rest of the anterior segment and fundus examination was normal. No abnormality was detected in the right eye. The best corrected visual acuity of 6/6 OD and 6/9 OS was achieved with spectacle correction at 6 months of follow-up. This case is a rare presentation of unilateral atypical coloboma located temporally without any iris abnormality and posterior segment coloboma or any other ocular or systemic anomaly. Early correction of refractive error and astigmatism results in good prognosis.
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