Correspondence
Eye (2010) 24, 944–945; doi:10.1038/eye.2009.194; published online 31 July 2009
Propionibacterium acnes endogenous endophthalmitis presenting with bilateral scleritis and uveitis
- 1Singapore National Eye Centre, Singapore
- 2Department of Ophthalmology, Yong Yoo Lin School of Medicine, National University of Singapore, Singapore
- 3Singapore Eye Research Institute, Singapore
Correspondence: S-P Chee, E-mail: chee.soon.phaik@snec.com.sg
Sir,
Propionibacterium acnes is known to cause delayed-onset postoperative endophthalmitis.1 Endogenous endophthalmitis, however, is very rare.2, 3
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Patient's right (a) and left (b) eyes with non-necrotising, diffuse anterior scleritis. Dendritic keratic precipitates were seen in both eyes (c=right, d=left), seen more clearly in the right, with anterior chamber cells 2+, flare 2+, and 360 degrees of posterior synechiae.
Full figure and legend (124K)
Posterior segment examination revealed mild vitritis in the right (a) and left (b)
eyes. There was no evidence of chorioretinitis, vasculitis, macula
oedema, or disc swelling. Posterior segment photos 18 months
post-presentation with no evidence of inflammation in both eyes (c=right eye; d=left eye).
Full figure and legend (90K)
Case report
A
55-year-old healthy Chinese lady with no past medical or surgical
history had a 1-week history of bilateral eye redness, blurring of
vision, and floaters. On examination, she was septic, with fever of
39.0°C and seemed unwell. Her best-corrected visual acuities (BCVA) were
6/15 OD, 6/24 OS. She had diffuse non-necrotising anterior scleritis, anterior chamber cells and flare 2+, posterior synechiae of 270–360 degrees, and small dendritiform keratic precipitates OU, but no iris nodules were seen (Figure 1a–d). There was mild vitritis OU (Figure 2a and b). Intra-ocular pressures were normal. Screening blood tests revealed a raised total white cell count (21.27 × 109/l) and erythrocyte sedimentation rate (103 mm/h).
Other investigations for infective agents, including blood cultures,
were non-contributory; whereas, an echocardiogram to rule out infective
endocarditis should have been done. An aqueous sample taken at the
slit-lamp with aseptic precautions was sent for Gram-staining, culture,
and PCR analysis. The initial culture results after 1 week and PCR
analysis were negative. She was treated empirically with intravenous
(IV) ceftriaxone (1.5 g BD) for a week and oral doxycycline (100 mg BD) with oral prednisolone (40 mg/day). Topical prednisolone acetate (1% hourly) and oral ibuprofen (400 mg
TDS) were added 5 days later. All initial culture results were
negative. At 15 days after presentation, the aqueous sample cultured P. acnes. As her ocular inflammation worsened, she was treated with IV crystalline penicillin (3 g every 4 h) and topical moxifloxacin on a 3-hour routine to which she responded clinically within 2 days. Her BCVA was 6/9 OU at 18 months with no recurrence of ocular inflammation (Figure 2c and d). However, the source of infection could not be identified.
Figure 1.
Patient's right (a) and left (b) eyes with non-necrotising, diffuse anterior scleritis. Dendritic keratic precipitates were seen in both eyes (c=right, d=left), seen more clearly in the right, with anterior chamber cells 2+, flare 2+, and 360 degrees of posterior synechiae.Full figure and legend (124K)
Figure 2.
Posterior segment examination revealed mild vitritis in the right (a) and left (b)
eyes. There was no evidence of chorioretinitis, vasculitis, macula
oedema, or disc swelling. Posterior segment photos 18 months
post-presentation with no evidence of inflammation in both eyes (c=right eye; d=left eye).Full figure and legend (90K)
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Comments
This is the first reported case, to our knowledge, of P. acnes endogenous endophthalmitis with bilateral panscleritis, and anterior and intermediate uveitis. Previous reports of P. acnes endogenous endophthalmitis have been based on immunocompromised individuals.1, 2 These cases presented with low-grade, granulomatous inflammation, which is dissimilar from our patient's presentation.3, 4
Our patient's dendritiform keratic precipitates were suggestive of an
infectious aetiology, prompting an aqueous sample culture and isolation
of the agent. Although this may be a contaminant, the isolation of this
fastidious organism and the rapid response to the second treatment
regime makes this unlikely.
Bilateral scleritis is an
unusual clinical manifestation of an endogenous infection, which may
represent an immune-mediated response to an ocular or systemic
infection. P. acnes can generate degradation enzymes and proteins that are immunogenic.5
This may account for the pathogenesis of our patient's clinical
manifestations. Similar pathogenesis has been suggested in cases of
ocular sarcoidosis, in which P. acnes was cultured from the vitreous.5 Although rare, the clinician should be aware that P. acnes
might be a cause of such a clinical manifestation so that rapid,
appropriate management may be instituted. With the development of new
molecular techniques, we may be able to detect the contributions of
microorganisms in the pathogenesis of ‘idiopathic’ ocular inflammation.
Conflict of interest
The authors declare no conflict of interest.
References
- De la Fuente J, Fernández-Catalina P, Sopeña B, Cadarso L. Endogenous endophthalmitis caused by Propionibacterium acnes. Arch Ophthalmol 1993; 111(11): 1468. | PubMed | ChemPort |
- Montero JA, Ruiz-Moreno JM, Rodríguez AE, Ferrer C, Sanchis E, Alio JL. Endogenous endophthalmitis by Propionibacterium acnes associated with leflunomide and adalimumab therapy. Eur J Ophthalmol 2006; 16(2): 343–345. | PubMed | ChemPort |
- Deramo VA, Ting TD. Treatment of Propionibacterium acnes endophthalmitis. Curr Opin Ophthalmol 2001; 12(3): 225–229. Review. | Article | PubMed | ChemPort |
- Aldave AJ, Stein JD, Deramo VA, Shah GK, Fischer DH, Maguire JI. Treatment strategies for postoperative Propionibacterium acnes endophthalmitis. Ophthalmology 1999; 106(12): 2395–2401. | Article | PubMed | ISI | ChemPort |
- Liu DT, Li CL, Lee VY. The presence of Propionibacterium spp. in the vitreous fluid of uveitis patients with sarcoidosis. Acta Ophthalmol Scand 2006; 84(1): 152–153.
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Acknowledgements
Contributions
of Authors: CSP was involved in the design of the study, MA and CSP in
the conduct of the study, MA and CSP in the management, analysis, and
interpretation of the data, and MA and CSP in the preparation, review,
or approval of the manuscript. This study was carried out with approval
from our Institutional Review Board (Singapore Eye Research Institute/Singhealth).
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