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A child with a rare presentation of ocular bartonellosis
A 6-year-old boy was referred from the optometrist for bilateral painless blurred vision of 2 weeks duration during routine screening. Upon examination, best-corrected visual acuity was 20/200 (right eye) and 20/120 (left eye). Anterior segment examination was normal for both eyes. Funduscopy showed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493987/ https://www.ncbi.nlm.nih.gov/pubmed/34703746 http://dx.doi.org/10.4103/tjo.tjo_29_20 |
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author | Shariffudin, Nor Syahira Min, Teh Wee Adnan, Azian Hashim, Hanizasurana Teo, Khairy Shamel Sonny |
author_facet | Shariffudin, Nor Syahira Min, Teh Wee Adnan, Azian Hashim, Hanizasurana Teo, Khairy Shamel Sonny |
author_sort | Shariffudin, Nor Syahira |
collection | PubMed |
description | A 6-year-old boy was referred from the optometrist for bilateral painless blurred vision of 2 weeks duration during routine screening. Upon examination, best-corrected visual acuity was 20/200 (right eye) and 20/120 (left eye). Anterior segment examination was normal for both eyes. Funduscopy showed bilateral optic disc swelling with peripapillary exudates and diffuse retinochoroiditis involving the posterior pole. Optical coherence tomography revealed diffuse retinal thickening with intraretinal fluids and cystoid changes of central fovea. Fluorescein angiography showed bilateral hot discs with vasculitis in all quadrants and large areas of nonperfusion at peripheral retina. The patient was initially treated as presumed ocular tuberculosis (TB) based on clinical presentation and history of contact with family member having pulmonary TB. Antituberculous therapy was started and both eyes received panretinal laser photocoagulation. After 3 weeks of anti-TB treatment, serology for Bartonella turned out to be positive. Treatment was changed to intravenous ceftriaxone for 10 days followed by oral cotrimoxazole for 6 weeks and combined treatment with oral prednisolone. Gradual clinical improvement was seen with corresponding visual gain due to the reduction of macular edema, but residual thickening remained due to its chronicity. |
format | Online Article Text |
id | pubmed-8493987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-84939872021-10-25 A child with a rare presentation of ocular bartonellosis Shariffudin, Nor Syahira Min, Teh Wee Adnan, Azian Hashim, Hanizasurana Teo, Khairy Shamel Sonny Taiwan J Ophthalmol Case Report A 6-year-old boy was referred from the optometrist for bilateral painless blurred vision of 2 weeks duration during routine screening. Upon examination, best-corrected visual acuity was 20/200 (right eye) and 20/120 (left eye). Anterior segment examination was normal for both eyes. Funduscopy showed bilateral optic disc swelling with peripapillary exudates and diffuse retinochoroiditis involving the posterior pole. Optical coherence tomography revealed diffuse retinal thickening with intraretinal fluids and cystoid changes of central fovea. Fluorescein angiography showed bilateral hot discs with vasculitis in all quadrants and large areas of nonperfusion at peripheral retina. The patient was initially treated as presumed ocular tuberculosis (TB) based on clinical presentation and history of contact with family member having pulmonary TB. Antituberculous therapy was started and both eyes received panretinal laser photocoagulation. After 3 weeks of anti-TB treatment, serology for Bartonella turned out to be positive. Treatment was changed to intravenous ceftriaxone for 10 days followed by oral cotrimoxazole for 6 weeks and combined treatment with oral prednisolone. Gradual clinical improvement was seen with corresponding visual gain due to the reduction of macular edema, but residual thickening remained due to its chronicity. Wolters Kluwer - Medknow 2020-08-14 /pmc/articles/PMC8493987/ /pubmed/34703746 http://dx.doi.org/10.4103/tjo.tjo_29_20 Text en Copyright: © 2020 Taiwan J Ophthalmol https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Shariffudin, Nor Syahira Min, Teh Wee Adnan, Azian Hashim, Hanizasurana Teo, Khairy Shamel Sonny A child with a rare presentation of ocular bartonellosis |
title | A child with a rare presentation of ocular bartonellosis |
title_full | A child with a rare presentation of ocular bartonellosis |
title_fullStr | A child with a rare presentation of ocular bartonellosis |
title_full_unstemmed | A child with a rare presentation of ocular bartonellosis |
title_short | A child with a rare presentation of ocular bartonellosis |
title_sort | child with a rare presentation of ocular bartonellosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493987/ https://www.ncbi.nlm.nih.gov/pubmed/34703746 http://dx.doi.org/10.4103/tjo.tjo_29_20 |
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