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儿童纤维蛋白溶酶原缺乏症性结膜炎的治疗。

Management of ligneous conjunctivitis in a child with plasminogen deficiency.

机构信息

Haemophilia Centre/Haemostasis Unit, Aghia Sophia Children's Hospital, Athens GR11527, Greece.

出版信息

Eur J Pediatr. 2011 Oct;170(10):1333-6. doi: 10.1007/s00431-011-1483-9. Epub 2011 May 31.

Abstract

UNLABELLED

Plasminogen deficiency, a rare autosomal recessive disorder, is classified as type I (hypoplasminogenemia) or type II (dysplasminogenemia). Hypoplasminogenemia is characterized by impaired wound healing while ligneous conjunctivitis (LC) is its main manifestation presenting with redness of the conjunctivae and progression to pseudomembranes' formation on the palpebral surfaces. A 4-year-old girl with LC in her left eye and impaired vision was referred to our unit. The conjunctival membranes had been already excised twice, followed by recurrences. Soon after the third recurrence, a probable diagnosis of LC was suggested, confirmed by a reduced plasminogen activity at 20% (normal values 80-120%). Both of her parents have slightly reduced plasminogen levels (50-60%) without any relevant symptom. Fresh frozen plasma (FFP) was administered systemically and topically, initiating 2 days before surgical removal of pseudomembranes with electrocautery under general anaesthesia. Systemic FFP was administered for 12 days postoperatively, along with topical use; the later was continued thereafter for 3 months. No recurrence was noticed. The vision was improved. Two weeks after cessation of the topical treatment, pseudomembranes reappeared. Topical application of FFP was reinitiated soon thereafter, and the girl underwent a second operation to have the conjunctival pseudomembranes removed. The perioperative therapeutic management was as previously described. Systemic treatment was stopped at the end of the tenth day while topical application of FFP was being continued until now, 10 months postoperatively. No recurrence has been observed and the vision remains at 9/10.

CONCLUSION

Since surgical excision of the conjunctival pseudomembranes alone in patients with LC does not protect from recurrences, the perioperative administration of FFP, both systemically and topically improves the outcome. Furthermore, the long-term application of topical FFP preparations seems to prevent recurrences and has a protective effect on the vision of these patients.

摘要

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纤溶酶原缺乏症是一种罕见的常染色体隐性遗传病,可分为 I 型(纤溶酶原血症)或 II 型(异常纤溶酶原血症)。纤溶酶原血症的特征是伤口愈合受损,而木样结膜炎(LC)是其主要表现,表现为结膜发红,并进展为睑表面伪膜形成。一名左眼患有 LC 和视力受损的 4 岁女孩被转介到我们科室。结膜膜已经切除了两次,随后又复发了。在第三次复发后不久,就提示可能是 LC,通过检测到纤溶酶原活性降低至 20%(正常值为 80-120%)得到确认。她的父母两人的纤溶酶原水平略有降低(50-60%),但没有任何相关症状。在全身麻醉下用电烙术切除伪膜之前,系统和局部给予新鲜冷冻血浆(FFP),开始于 2 天前。术后给予 12 天的全身 FFP 治疗,并局部使用;此后,局部使用持续了 3 个月。没有发现复发。视力得到改善。停药两周后,伪膜再次出现。随后很快重新开始局部应用 FFP,女孩接受了第二次手术以切除结膜伪膜。围手术期治疗管理如前所述。术后第 10 天停止全身治疗,同时继续局部应用 FFP,至今已术后 10 个月。没有复发,视力保持在 9/10。

结论

由于单独切除 LC 患者的结膜伪膜并不能防止复发,因此围手术期给予 FFP 全身和局部应用可改善结果。此外,长期局部应用 FFP 制剂似乎可以防止复发,并对这些患者的视力有保护作用。

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