Microspherophakia and Lens Subluxation in Klinefelter Syndrome: A Case Report.

IF 1.2 Q3 OPHTHALMOLOGY
Journal of Current Ophthalmology Pub Date : 2023-12-21 eCollection Date: 2023-04-01 DOI:10.4103/joco.joco_291_22
Jana Van Laeken, Laura Leysen, Karel Van Keer
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引用次数: 0

Abstract

Purpose: To report a rare case of microspherophakia and lens subluxation in a young patient with Klinefelter syndrome who underwent cataract surgery, emphasizing the importance of a thorough general health assessment and anamnesis prior to cataract surgery.

Methods: The case concerns a 52-year-old male referred for phacoemulsification under general anesthesia. A review of literature was performed.

Results: Preoperative assessment revealed a corticonuclear cataract in both eyes, with dislocation of the crystalline lens in the left eye in an area of zonular dehiscence. Upon careful examination, both eyes showed a microspherophakic lens with an increased lens thickness and the lens equator being visible over 360° in the left eye. The patient denied any trauma or medical conditions. His medical health record revealed the coexistence of Klinefelter syndrome (47, XXY). The association between Klinefelter syndrome and microspherophakia has only once been reported in the literature. Intraoperatively, a more cautious approach was withheld and a capsular tension ring was used. Postoperative outcome was successful with good visual outcome and no interoperative complications.

Conclusions: This case report highlights the importance of proper preoperative assessment before cataract surgery, especially in unusual cases such as early-onset cataract and/or lens subluxation. In addition, it stresses the importance of a systemic and/or genetic evaluation in patients with microspherophakia and an ophthalmological examination in patients with Klinefelter syndrome.

Klinefelter 综合征中的小球盲和晶状体半脱位:病例报告
目的:报告一例罕见的微小球窗症和晶状体半脱位病例,该病例患有 Klinefelter 综合征,并接受了白内障手术:该病例涉及一名 52 岁的男性,他在全身麻醉下接受了白内障超声乳化手术。方法:病例涉及一名 52 岁男性,在全身麻醉下接受超声乳化术,并回顾了相关文献:术前评估显示双眼均为皮质核性白内障,左眼晶状体脱位,位于眼球裂孔区。经仔细检查,双眼均显示出微球泡状晶状体,左眼晶状体厚度增加,晶状体赤道部 360° 以上可见。患者否认有任何外伤或疾病。他的医疗记录显示,他同时患有克莱恩费尔特综合征(47,XXY)。Klinefelter 综合征与小球幕症之间的关联仅在文献中报道过一次。术中,医生采用了更为谨慎的方法,并使用了囊状张力环。术后效果良好,视觉效果良好,无术中并发症:本病例报告强调了在白内障手术前进行适当术前评估的重要性,尤其是对于不常见的病例,如早发白内障和/或晶状体半脱位。此外,报告还强调了对小球海绵体白内障患者进行系统和/或遗传学评估以及对克莱恩费尔特综合征患者进行眼科检查的重要性。
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来源期刊
CiteScore
2.50
自引率
6.70%
发文量
45
审稿时长
8 weeks
期刊介绍: Peer Review under the responsibility of Iranian Society of Ophthalmology Journal of Current Ophthalmology, the official publication of the Iranian Society of Ophthalmology, is a peer-reviewed, open-access, scientific journal that welcomes high quality original articles related to vision science and all fields of ophthalmology. Journal of Current Ophthalmology is the continuum of Iranian Journal of Ophthalmology published since 1969.
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