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Published in: BMC Ophthalmology 1/2016

Open Access 01-12-2016 | Case report

Rabbit hunter uveitis: case report of tularemia uveitis

Authors: Céline Terrada, Said Azza, Bahram Bodaghi, Phuc Le Hoang, Michel Drancourt

Published in: BMC Ophthalmology | Issue 1/2016

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Abstract

Background

Literature reports on ophthalmological manifestations related to tularemia, a zoonose caused by the bacterium Francisella tularensis, largely refer to Parinaud’s oculoglandular syndrome, which consists of the association of conjunctivitis with preauricular lymphadenitis. In this paper, we report a case of intraocular inflammation during tularemia infection.

Case presentation

A 52-year-old Caucasian man was diagnosed with unilateral uveitis. The uveitis was posterior, with a 2+ vitritis and a large yellowish lesion involving the macula with an overlying sub-retinal detachment, extending inferiorly, and subretinal hemorrhages. Fluorescein angiography showed a late hyperfluorescence with focal vascular leakage. Ultrasound biomicroscopy confirmed the presence of a 3.8 mm parietal granuloma with a few calcifications in the left eye. While extensive work-up eliminated any other infectious and non-infectious etiology, tularemia was diagnosed by advanced serology consisting of two-dimensional Western-immunoblotting. The patient, a hunter, recalled having killed rabbits in the days before the symptoms appeared. Uveitis was rapidly controlled following treatment with doxycycline, yet three years after initiation of the treatment, the patient still complained of loss of vision in the left eye with a central scotoma.

Conclusions

Posterior uveitis may be an infrequent manifestation of tularemia infection, and therefore this infection should be considered in the differential diagnosis of intraocular inflammation in areas where F. tularensis is endemic.
Literature
2.
go back to reference Thompson S, Omphroy L, Oetting T. Parinaud’s oculoglandular syndrome attributable to an encounter with a wild rabbit. Am J Ophthalmol. 2001;131:283–4.CrossRefPubMed Thompson S, Omphroy L, Oetting T. Parinaud’s oculoglandular syndrome attributable to an encounter with a wild rabbit. Am J Ophthalmol. 2001;131:283–4.CrossRefPubMed
3.
go back to reference Portero A, Careño E, Real LA, Villarón S, Herreras JM. Infectious nontuberculous serpiginous choroiditis. Arch Ophthalmol. 2012;130:1207–8.CrossRefPubMed Portero A, Careño E, Real LA, Villarón S, Herreras JM. Infectious nontuberculous serpiginous choroiditis. Arch Ophthalmol. 2012;130:1207–8.CrossRefPubMed
4.
go back to reference Drancourt M, Berger P, Terrada C, Bodaghi B, Conrath J, Raoult D, LeHoang P. High prevalence of fastidious bacteria in 1520 cases of uveitis of unknown etiology. Medicine (Baltimore). 2008;87:167–76.CrossRef Drancourt M, Berger P, Terrada C, Bodaghi B, Conrath J, Raoult D, LeHoang P. High prevalence of fastidious bacteria in 1520 cases of uveitis of unknown etiology. Medicine (Baltimore). 2008;87:167–76.CrossRef
5.
go back to reference Fournier PE, Bernabeu L, Schubert B, Mutillod M, Roux V, Raoult D. Isolation of Francisella tularensis by centrifugation of shell vial cell culture from an inoculation eschar. J Clin Microbiol. 1998;36:2782–3.PubMedPubMedCentral Fournier PE, Bernabeu L, Schubert B, Mutillod M, Roux V, Raoult D. Isolation of Francisella tularensis by centrifugation of shell vial cell culture from an inoculation eschar. J Clin Microbiol. 1998;36:2782–3.PubMedPubMedCentral
6.
go back to reference Eyles JE, Unal B, Hartley MG, Newstead SL, Flick-Smith H, Prior JL, Oyston PC, Randall A, Mu Y, Hirst S, Molina DM, Davies DH, Milne T, Griffin KF, Baldi P, Titball RW, Felgner PL. Immunodominant Francisella tularensis antigens identified using proteome microarray. Proteomics. 2007;7:2172–83.CrossRefPubMed Eyles JE, Unal B, Hartley MG, Newstead SL, Flick-Smith H, Prior JL, Oyston PC, Randall A, Mu Y, Hirst S, Molina DM, Davies DH, Milne T, Griffin KF, Baldi P, Titball RW, Felgner PL. Immunodominant Francisella tularensis antigens identified using proteome microarray. Proteomics. 2007;7:2172–83.CrossRefPubMed
7.
go back to reference Ang M, Htoon HM, Chee SP. Diagnosis of tuberculous uveitis: clinical application of an interferon-gamma release assay. Ophthalmology. 2009;116:1391–6.CrossRefPubMed Ang M, Htoon HM, Chee SP. Diagnosis of tuberculous uveitis: clinical application of an interferon-gamma release assay. Ophthalmology. 2009;116:1391–6.CrossRefPubMed
8.
go back to reference Matonti F, Conrath J, Bodaghi B, Le Hoang P, Raoult D, Drancourt M. Uveitis in the course of Q-fever. Clin Microbiol Infect. 2009;15:176–7.CrossRefPubMed Matonti F, Conrath J, Bodaghi B, Le Hoang P, Raoult D, Drancourt M. Uveitis in the course of Q-fever. Clin Microbiol Infect. 2009;15:176–7.CrossRefPubMed
9.
go back to reference Million M, Halfon J, Le Lez ML, Drancourt M, Raoult D. Relapsing uveitis and optic neuritis due to chronic Q fever. Br J Ophthalmol. 2011;95:1026–7.CrossRefPubMed Million M, Halfon J, Le Lez ML, Drancourt M, Raoult D. Relapsing uveitis and optic neuritis due to chronic Q fever. Br J Ophthalmol. 2011;95:1026–7.CrossRefPubMed
Metadata
Title
Rabbit hunter uveitis: case report of tularemia uveitis
Authors
Céline Terrada
Said Azza
Bahram Bodaghi
Phuc Le Hoang
Michel Drancourt
Publication date
01-12-2016
Publisher
BioMed Central
Published in
BMC Ophthalmology / Issue 1/2016
Electronic ISSN: 1471-2415
DOI
https://doi.org/10.1186/s12886-016-0332-z

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