ATYPICAL FORMS OF EYE TOXOPLASMOSIS IN CHILDHOOD. CASE REPORTS
Language English Country Czech Republic Media print
Document type Case Reports, Journal Article
PubMed
36220366
DOI
10.31348/2022/27
PII: 131899
Knihovny.cz E-resources
- Keywords
- Professor Janků, Toxoplasmosis, hypogammaglobulinaemia, intraocular neuritis, retinal vasculitis, retinochoroiditis, varicella,
- MeSH
- Agammaglobulinemia * drug therapy MeSH
- Anti-Bacterial Agents therapeutic use MeSH
- Chorioretinitis * drug therapy MeSH
- Child MeSH
- Adult MeSH
- Adrenal Cortex Hormones MeSH
- Immunoglobulin A therapeutic use MeSH
- Immunoglobulin G therapeutic use MeSH
- Immunoglobulin M therapeutic use MeSH
- Immunosuppressive Agents therapeutic use MeSH
- Humans MeSH
- Macrolides therapeutic use MeSH
- Adolescent MeSH
- Young Adult MeSH
- Neuritis * drug therapy MeSH
- Toxoplasmosis, Ocular * complications diagnosis MeSH
- Retinal Vasculitis * drug therapy MeSH
- Blindness drug therapy MeSH
- Toxoplasma * MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Adrenal Cortex Hormones MeSH
- Immunoglobulin A MeSH
- Immunoglobulin G MeSH
- Immunoglobulin M MeSH
- Immunosuppressive Agents MeSH
- Macrolides MeSH
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.
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