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...
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Wolters Kluwer Medknow Publications
2021-01-01
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doaj-1ce3ed0604ee4075a1ca6e42949e62db2021-10-07T05:55:20ZengWolters Kluwer Medknow PublicationsTaiwan Journal of Ophthalmology2211-50562211-50722021-01-0111329229510.4103/tjo.tjo_29_20A child with a rare presentation of ocular bartonellosisNor Syahira ShariffudinTeh Wee MinAzian AdnanHanizasurana HashimKhairy Shamel Sonny TeoA 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.http://www.e-tjo.org/article.asp?issn=2211-5056;year=2021;volume=11;issue=3;spage=292;epage=295;aulast=Shariffudincat scratch diseaseneuroretinitisocclusive vasculitisocular bartonellosisretinochoroiditis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nor Syahira Shariffudin Teh Wee Min Azian Adnan Hanizasurana Hashim Khairy Shamel Sonny Teo |
spellingShingle |
Nor Syahira Shariffudin Teh Wee Min Azian Adnan Hanizasurana Hashim Khairy Shamel Sonny Teo A child with a rare presentation of ocular bartonellosis Taiwan Journal of Ophthalmology cat scratch disease neuroretinitis occlusive vasculitis ocular bartonellosis retinochoroiditis |
author_facet |
Nor Syahira Shariffudin Teh Wee Min Azian Adnan Hanizasurana Hashim Khairy Shamel Sonny Teo |
author_sort |
Nor Syahira Shariffudin |
title |
A child with a rare presentation of ocular bartonellosis |
title_short |
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_sort |
child with a rare presentation of ocular bartonellosis |
publisher |
Wolters Kluwer Medknow Publications |
series |
Taiwan Journal of Ophthalmology |
issn |
2211-5056 2211-5072 |
publishDate |
2021-01-01 |
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. |
topic |
cat scratch disease neuroretinitis occlusive vasculitis ocular bartonellosis retinochoroiditis |
url |
http://www.e-tjo.org/article.asp?issn=2211-5056;year=2021;volume=11;issue=3;spage=292;epage=295;aulast=Shariffudin |
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