ATYPICAL FORMS OF EYE TOXOPLASMOSIS IN CHILDHOOD. CASE REPORTS.

Q4 Medicine
J Krásný, J Šach, E Daňková
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引用次数: 0

Abstract

Aim: To present an outline of acquired atypical forms of ocular toxoplasmosis (OT) in childhood, with reference to the 100th anniversary of the discovery of this etiology by Professor Janků from Czechoslovakia, who was first to describe the clinical congenital picture of OT characterised by macular scar.

Material and methods: Symptoms of intraocular bilateral neuritis appeared in a 6-year-old girl, with visual acuity (VA) bilaterally 0.1. Toxoplasmic etiology was demonstrated in laboratory tests, and the patient was immunocompetent. Following treatment with macrolide antibiotic and parabulbar application of corticosteroid, the condition was normalised stably at VA 1.0 in both eyes. Bilateral retinal vasculitis was determined in an 8-year-old boy, with VA of 0.25 in the right eye and 0.25 in the left, with a medical history of strabismus detected after suffering from varicella. The examination for toxoplasmosis was negative, but pronounced general hypogammaglobulinaemia classes IgG, IgM and IgA was detected. Immunosuppressive and immunomodulatory therapy did not produce the desired effect, and the condition progressed to retinochoroiditis. Due to blindness and dolorous glaucoma, enucleation of the right eye was performed at the age of 15 years. Histologically toxoplasmic cysts with bradyzoites were detected, a subsequent laboratory test demonstrated toxoplasmic etiology upon a background of persistent regressing hypogammaglobulinaemia. General anti-toxoplasma and subsequent immunosuppressive treatment did not produce the desired effect, and at the age of 22 years the patient lost his sight also in the left eye.

Conclusion: Atypical form of OT intraocular neuritis in an immunocompetent patient had a favourable course, whereas retinal vasculitis with retinochoroiditis in a temporarily immunocompromised patient ended in bilateral blindness.

儿童眼弓形虫病的非典型形式。案例报告。
目的:介绍儿童获得性非典型眼弓形虫病(OT)的概况,并参考jank教授发现这种病因100周年;来自捷克斯洛伐克,谁是第一个描述临床先天性图片的黄斑疤痕特征的OT。材料与方法:6岁女童,双侧视力0.1,出现双侧眼内神经炎症状。弓形虫病原学在实验室检查中得到证实,患者具有免疫能力。经大环内酯类抗生素和球旁应用皮质类固醇治疗后,双眼VA稳定恢复正常,为1.0。患者为8岁男童,右眼VA为0.25,左眼为0.25,有水痘后斜视病史。弓形虫病检查阴性,但检测到明显的一般低丙种球蛋白类IgG、IgM和IgA。免疫抑制和免疫调节治疗没有产生预期的效果,病情进展为视网膜脉络膜炎。由于失明和忧郁性青光眼,在15岁时进行了右眼摘除手术。组织学上发现弓形虫囊肿伴慢殖子,随后的实验室检查证实弓形虫病因是持续消退的低γ球蛋白血症。一般的抗弓形虫和随后的免疫抑制治疗没有产生预期的效果,在22岁时,患者左眼也失去了视力。结论:免疫功能正常患者的非典型OT眼内神经炎有良好的病程,而暂时性免疫功能低下患者的视网膜血管炎伴视网膜脉络膜炎最终导致双侧失明。
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来源期刊
Ceska a Slovenska Oftalmologie
Ceska a Slovenska Oftalmologie Medicine-Ophthalmology
CiteScore
0.80
自引率
0.00%
发文量
0
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