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依赖输血的β地中海贫血患者的眼部表现

Ocular manifestations in patients with transfusion-dependent β-thalassemia.

作者信息

Akritidou F, Praidou A, Papamitsou T, Kozobolis V, Labiris G

机构信息

Department of Ophthalmology, General Hospital of Serres, Greece.

Department of Ophthalmology, General Hospital of Thessaloniki "G.Gennimatas-O Agios Dimitrios", Thessaloniki, Greece.

出版信息

Hippokratia. 2021 Apr-Jun;25(2):79-82.

Abstract

BACKGROUND

Ocular involvement in patients with transfusion-dependent β-thalassemia is quite common, and its frequency differs among studies. This case series aimed to describe the ocular abnormalities occurring in β-thalassemia patients who need regular blood transfusions and receive iron chelation therapy.

CASE SERIES

This is a case series prospectively studied 32 β-thalassemia patients from Northern Greece receiving regular blood transfusions and iron-chelating therapy. Patients' average age was 35.5 years. Eighteen patients with major phenotypes and fourteen patients with intermedia type underwent comprehensive ophthalmic examination at the time of enrolment, including visual acuity evaluation, refraction and color vision tests, Amsler grid test, slit-lamp, and dilated-pupil fundus examination. Additionally, we performed visual field testing and optical coherence tomography in all patients and fluorescein angiography only in selected cases. After six months, patients' complete ophthalmic examination was repeated for any new ocular findings due to the disease process and iron chelation therapy. Ocular involvement was detected in 46.87 % of the patients. Lesions were most frequently seen in elderly patients with thalassemia major. Lens opacities were present in 21.8 %, and degeneration of the retinal pigment epithelium was described in 15.6 % of the patients, representing the commonest fundus alteration observed, followed by fundus atrophy. The most severe and vision-threatening condition described in this study was the presence of angioid streaks with choroidal neovascularisation. Six months follow-up of patients did not reveal any new ocular findings.

CONCLUSION

Early detection of severe ocular abnormalities is important in patients with thalassemia; thus, an ophthalmologic examination should be included at regular check-ups. An annual examination is currently indicated for asymptomatic patients, while in symptomatic and complicated cases, patients should be closely followed-up. HIPPOKRATIA 2021, 25 (2):79-82.

摘要

背景

输血依赖型β地中海贫血患者眼部受累颇为常见,不同研究报告的发生率有所差异。本病例系列旨在描述需定期输血并接受铁螯合治疗的β地中海贫血患者出现的眼部异常情况。

病例系列

这是一个前瞻性研究的病例系列,纳入了32例来自希腊北部、接受定期输血和铁螯合治疗的β地中海贫血患者。患者的平均年龄为35.5岁。18例重型患者和14例中间型患者在入组时接受了全面的眼科检查,包括视力评估、验光和色觉测试、阿姆斯勒方格表检查、裂隙灯检查以及散瞳眼底检查。此外,我们对所有患者进行了视野测试和光学相干断层扫描,仅对部分病例进行了荧光素血管造影。六个月后,因疾病进展和铁螯合治疗出现任何新的眼部发现时,再次对患者进行全面的眼科检查。46.87%的患者检测到眼部受累。病变最常见于老年重型地中海贫血患者。21.8%的患者出现晶状体混浊,15.6%的患者出现视网膜色素上皮变性,这是观察到的最常见的眼底改变,其次是眼底萎缩。本研究中描述的最严重且威胁视力的情况是出现血管样条纹伴脉络膜新生血管形成。对患者进行六个月的随访未发现任何新的眼部发现。

结论

早期发现地中海贫血患者的严重眼部异常很重要;因此,定期检查应包括眼科检查。目前,无症状患者建议每年检查一次,而有症状和复杂病例的患者应密切随访。《希波克拉底》2021年,第25卷(第2期):79 - 82页 。

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本文引用的文献

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Gene Therapy For Beta-Thalassemia: Updated Perspectives.β地中海贫血的基因治疗:最新观点
Appl Clin Genet. 2019 Sep 23;12:167-180. doi: 10.2147/TACG.S178546. eCollection 2019.
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