open access

Vol 8 (2023): Continuous Publishing
Case report
Published online: 2023-03-31
Get Citation

Great imitator — ocular syphilis

Seher Koksaldi1, Mustafa Kayabasi1, Ali Osman Saatci1
·
Ophthalmol J 2023;8:13-18.
Affiliations
  1. Department of Ophthalmology, Dokuz Eylul University, Izmir, Türkiye

open access

Vol 8 (2023): Continuous Publishing
CASE REPORTS
Published online: 2023-03-31

Abstract

We examined a 44-year-old woman without any known systemic disease with a decreased vision of a month duration in her left eye. She had undergone left uneventful cataract surgery with intraocular lens implantation elsewhere 14 years ago. On examination, her Snellen visual acuity was 1.0 (with the correction of –0.50–0.25 × 120) in the right eye and 0.4 (with the correction of +0.75–2.25 × 115) in the left. There was left hypochromic heterochromia. While the right anterior segment was unremarkable, there were small to medium-sized keratic precipitates, 3+ anterior chamber cells, a posterior chamber intraocular lens with an intact posterior capsule, and a few vitreous cells in the left eye. Fundus autofluorescence imaging revealed peripapillary hyperautofluorescence in the left eye, and fluorescein angiography revealed a marked optic nerve head and perivascular leakage at the posterior pole. The findings were not compatible with Fuchs uveitis, so the full infectious panel was worked out. Serologic investigations yielded the presence of syphilis, and the patient was treated successfully with systemic antibiotics. Our case demonstrates the mimicking nature of ocular syphilis and the importance of high clinical suspicion when reaching the correct diagnosis.

Abstract

We examined a 44-year-old woman without any known systemic disease with a decreased vision of a month duration in her left eye. She had undergone left uneventful cataract surgery with intraocular lens implantation elsewhere 14 years ago. On examination, her Snellen visual acuity was 1.0 (with the correction of –0.50–0.25 × 120) in the right eye and 0.4 (with the correction of +0.75–2.25 × 115) in the left. There was left hypochromic heterochromia. While the right anterior segment was unremarkable, there were small to medium-sized keratic precipitates, 3+ anterior chamber cells, a posterior chamber intraocular lens with an intact posterior capsule, and a few vitreous cells in the left eye. Fundus autofluorescence imaging revealed peripapillary hyperautofluorescence in the left eye, and fluorescein angiography revealed a marked optic nerve head and perivascular leakage at the posterior pole. The findings were not compatible with Fuchs uveitis, so the full infectious panel was worked out. Serologic investigations yielded the presence of syphilis, and the patient was treated successfully with systemic antibiotics. Our case demonstrates the mimicking nature of ocular syphilis and the importance of high clinical suspicion when reaching the correct diagnosis.

Get Citation

Keywords

Fuchs’ heterochromic iridocyclitis; Fuchs uveitis; Fuchs uveitis syndrome; ocular syphilis

About this article
Title

Great imitator — ocular syphilis

Journal

Ophthalmology Journal

Issue

Vol 8 (2023): Continuous Publishing

Article type

Case report

Pages

13-18

Published online

2023-03-31

Page views

2130

Article views/downloads

346

DOI

10.5603/OJ.2023.0004

Bibliographic record

Ophthalmol J 2023;8:13-18.

Keywords

Fuchs’ heterochromic iridocyclitis
Fuchs uveitis
Fuchs uveitis syndrome
ocular syphilis

Authors

Seher Koksaldi
Mustafa Kayabasi
Ali Osman Saatci

References (20)
  1. Standardization of Uveitis Nomenclature (SUN) Working Group. Classification Criteria for Fuchs Uveitis Syndrome. Am J Ophthalmol. 2021; 228: 262–267.
  2. Jones NP. The Manchester Uveitis Clinic: the first 3000 patients--epidemiology and casemix. Ocul Immunol Inflamm. 2015; 23(2): 118–126.
  3. Ganesh SK, Sharma S, Narayana KM, et al. Fuchs' heterochromic iridocyclitis following bilateral ocular toxoplasmosis. Ocul Immunol Inflamm. 2004; 12(1): 75–77.
  4. Hashida N, Ohguro N, Maruyama H. Fuchs' heterochromic iridocyclitis associated with ocular toxocariasis. Jpn J Ophthalmol. 2011; 55(1): 76–78.
  5. Birnbaum AD, Tessler HH, Schultz KL, et al. Epidemiologic relationship between fuchs heterochromic iridocyclitis and the United States rubella vaccination program. Am J Ophthalmol. 2007; 144(3): 424–428.
  6. Chee SP, Jap A. Presumed fuchs heterochromic iridocyclitis and Posner-Schlossman syndrome: comparison of cytomegalovirus-positive and negative eyes. Am J Ophthalmol. 2008; 146(6): 883–889.e1.
  7. Barequet IS, Li Q, Wang Y, et al. Herpes simplex virus DNA identification from aqueous fluid in Fuchs heterochromic iridocyclitis. Am J Ophthalmol. 2000; 129(5): 672–673.
  8. Babu K, Murthy GJ. Chikungunya virus iridocyclitis in Fuchs' heterochromic iridocyclitis. Indian J Ophthalmol. 2012; 60(1): 73–74.
  9. Chowers I, Zamir E, Banin E, et al. Retinitis pigmentosa associated with Fuchs' heterochromic uveitis. Arch Ophthalmol. 2000; 118(6): 800–802.
  10. Goble RR, Murray PI. Fuchs' heterochromic uveitis and sarcoidosis. Br J Ophthalmol. 1995; 79(11): 1021–1023.
  11. Ruokonen PC, Metzner S, Ucer A, et al. Intraocular antibody synthesis against rubella virus and other microorganisms in Fuchs' heterochromic cyclitis. Graefes Arch Clin Exp Ophthalmol. 2010; 248(4): 565–571.
  12. Aggarwal RK, Luck J, Coster DJ. Horner's syndrome and Fuchs' heterochromic uveitis. Br J Ophthalmol. 1994; 78(12): 949.
  13. Özdamar Erol Y, İnanç M, Özdal P. Fuchs' Uveitis: Is It Different from What We Know? Ocul Immunol Inflamm. 2022; 30(1): 62–67.
  14. Yalçındağ FN, Özdal PC, Özyazgan Y, et al. BUST Study Group. Demographic and Clinical Characteristics of Uveitis in Turkey: The First National Registry Report. Ocul Immunol Inflamm. 2018; 26(1): 17–26.
  15. Bouchenaki N, Herbort CP. Fuchs' Uveitis: Failure to Associate Vitritis and Disc Hyperfluorescence with the Disease is the Major Factor for Misdiagnosis and Diagnostic Delay. Middle East Afr J Ophthalmol. 2009; 16(4): 239–244.
  16. Tugal-Tutkun I, Güney-Tefekli E, Kamaci-Duman F, et al. A cross-sectional and longitudinal study of Fuchs uveitis syndrome in Turkish patients. Am J Ophthalmol. 2009; 148(4): 510–515.e1.
  17. Zarei M, Abdollahi A, Darabeigi S, et al. An investigation on optic nerve head involvement in Fuchs uveitis syndrome using optical coherence tomography and fluorescein angiography. Graefes Arch Clin Exp Ophthalmol. 2018; 256(12): 2421–2427.
  18. Aldave AJ, King JA, Cunningham ET. Ocular syphilis. Curr Opin Ophthalmol. 2001; 12(6): 433–441.
  19. Karti O, Top Karti D, Ozkan Ozdemir H, et al. Coexistence of Papillitis and Posterior Placoid Chorioretinopathy as the Presenting Symptoms of Syphilis-Human Immunodeficiency Virus Coinfection. Neuroophthalmology. 2019; 43(3): 196–200.
  20. Oliver GF, Stathis RM, Furtado JM, et al. International Ocular Syphilis Study Group. Current ophthalmology practice patterns for syphilitic uveitis. Br J Ophthalmol. 2019; 103(11): 1645–1649.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

Publisher: VM Media Group sp. z o.o., Grupa Via Medica, 73 Świętokrzyska St., 80–180 Gdańsk

tel.:+48 58 310 94 94, faks:+48 58 320 94 60, e-mail: viamedica@viamedica.pl