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银屑病相关的进行性坏死性后巩膜炎:6年随访

Psoriasis-associated progressive necrotizing posterior scleritis: A 6-year follow-up.

作者信息

Amer Radgonde, Levinger Nadav

机构信息

Department of Ophthalmology, Hadassah Medical Center, Jerusalem, Israel.

出版信息

Eur J Ophthalmol. 2020 May;30(3):NP7-NP10. doi: 10.1177/1120672118823121. Epub 2019 Jan 14.

DOI:10.1177/1120672118823121
PMID:30638053
Abstract

PURPOSE

Posterior scleritis is the least frequent form of scleritis accounting for around 2%-8% of all scleritis cases. We aim to present the 6-year clinical course of a 62-year-old female patient with bilateral progressive necrotizing posterior scleritis who suffered from concurrent active psoriasis and psoriatic arthritis.

METHODS

Descriptive case report.

RESULTS

A middle-aged female patient was referred to our clinic because of left eye peripheral progressively enlarging white retinochoroidal lesions. Her previous work-up ruled out infectious and malignant etiologies. A second diagnostic vitrectomy was performed because of the slowly progressive and the atypical nature of the sectoral retinochoroidal patches in the retinal periphery. Again malignancy was ruled out. With the onset of cystoid macular edema and diffuse retinal vasculitis, which occurred concurrently with the reactivation of psoriasis and psoriatic arthritis, treatment was initiated with systemic immunosuppressants which initially included oral steroids and methotrexate and at the last follow-up 6 years after the first presentation included also cyclosporin and golimumab. Vision was preserved with quiescent uveitis and posterior scleritis.

CONCLUSION

Posterior scleritis is an uncommon condition and it is even rarer in the setting of psoriasis. The necrotizing inflammation observed in the present case and by others revealed sectoral progressive chorioretinitis as a clinical manifestation which may initially raise the suspicion of masquerade malignant and infectious etiologies. Detailed thorough history-taking remains the cornerstone in identifying the possible systemic associations even when occult or subclinical.

摘要

目的

后巩膜炎是巩膜炎中最不常见的类型,约占所有巩膜炎病例的2%-8%。我们旨在介绍一名62岁双侧进行性坏死性后巩膜炎女性患者的6年临床病程,该患者同时患有活动性银屑病和银屑病关节炎。

方法

描述性病例报告。

结果

一名中年女性患者因左眼周边视网膜脉络膜白色病变逐渐扩大而转诊至我院。她之前的检查排除了感染性和恶性病因。由于视网膜周边扇形视网膜脉络膜斑块进展缓慢且具有非典型性,进行了第二次诊断性玻璃体切除术。再次排除了恶性肿瘤。随着黄斑囊样水肿和弥漫性视网膜血管炎的出现,这与银屑病和银屑病关节炎的复发同时发生,开始使用全身免疫抑制剂治疗,最初包括口服类固醇和甲氨蝶呤,在首次就诊6年后的最后一次随访中还包括环孢素和戈利木单抗。葡萄膜炎和后巩膜炎静止,视力得以保留。

结论

后巩膜炎是一种罕见疾病,在银屑病患者中更为罕见。在本病例及其他病例中观察到的坏死性炎症显示扇形进行性脉络膜视网膜炎为一种临床表现,这可能最初会引发对伪装的恶性和感染性病因的怀疑。即使存在隐匿或亚临床情况,详细全面的病史采集仍然是识别可能的全身关联的基石。

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