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晶状体缺损

Coloboma of the crystalline lens.

作者信息

Ilsen Pauline F, Patel Shilla

机构信息

West Los Angeles VA Healthcare Center, Los Angeles, California, USA.

出版信息

Optometry. 2003 Dec;74(12):765-74.

Abstract

BACKGROUND

Anomalies of crystalline lens shape and position include: lenticonus, lentiglobus, microspherophakia, coloboma, and ectopia lentis. Lens coloboma probably results from a localized absence or maldevelopment of lens zonules. It may be a variant of nontraumatic (congenital) ectopia lentis, in which the zonular deficiency is more generalized. Coloboma of the lens and nontraumatic ectopia lentis may occur in association with other ocular and systemic anomalies. A case of lens coloboma is presented, and lens coloboma, ectopia lentis, and associated ocular and systemic conditions are reviewed.

CASE REPORT

A 36-year-old man came to us for routine evaluation. He was found to be moderately myopic. Post-dilated biomicroscopy revealed a crystalline lens coloboma O.D. Since the patient was tall and thin, and his chest X-ray demonstrated abnormal cardiovascular findings, Marfan's syndrome or another connective tissue disorder was suspected. No definitive diagnosis was established for the patient, but he later reported that his sister had Marfan's syndrome, renewing suspicion that he also had the condition. He was advised to wear polycarbonate spectacles and to avoid contact sports.

CONCLUSIONS

Coloboma of the crystalline lens and nontraumatic ectopia lentis may occur in isolation or with other ocular pathologies, and may reflect an underlying systemic disorder. Optometric management must address safety issues to reduce the risk of retinal detachment and lens dislocation. Systemic evaluation should be pursued to rule out Marfan's syndrome and similar disorders. Genetic investigation and evaluation of family members may also be merited.

摘要

背景

晶状体形状和位置异常包括:圆锥形晶状体、球形晶状体、小晶状体、缺损和晶状体异位。晶状体缺损可能是由于晶状体悬韧带局部缺失或发育不良所致。它可能是非创伤性(先天性)晶状体异位的一种变体,其中悬韧带缺陷更为普遍。晶状体缺损和非创伤性晶状体异位可能与其他眼部和全身异常同时出现。本文报告一例晶状体缺损病例,并对晶状体缺损、晶状体异位及相关眼部和全身情况进行综述。

病例报告

一名36岁男性前来我们处进行常规检查。发现他有中度近视。散瞳后生物显微镜检查发现右眼有晶状体缺损。由于该患者身材瘦高,胸部X线显示心血管异常,怀疑患有马凡综合征或其他结缔组织疾病。该患者未确诊,但他后来报告说他的姐姐患有马凡综合征,这再次引发了对他也患有该病的怀疑。建议他佩戴聚碳酸酯眼镜并避免接触性运动。

结论

晶状体缺损和非创伤性晶状体异位可能单独出现或与其他眼部病变同时出现,可能反映潜在的全身疾病。验光管理必须解决安全问题,以降低视网膜脱离和晶状体脱位的风险。应进行全身评估以排除马凡综合征和类似疾病。对家庭成员进行基因调查和评估也可能是有必要的。

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