Scientifica / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 6313070 | 4 pages |

A Pathological Analysis of Canaliculitis Concretions: More Than Just Actinomyces

Academic Editor: John W. Hiemenz
Received02 Feb 2016
Accepted23 May 2016
Published14 Jun 2016


Purpose. Canaliculitis is classically associated with Actinomyces species, which are filamentous bacteria; the purpose of this study was to evaluate the extent to which nonfilamentous bacteria colonize canalicular concretions by using graded histopathological analysis. Methods. This is a series of 16 cases. The percentage of Gram-positive/Gomori’s methenamine silver-positive filamentous bacteria (Actinomyces) versus the total bacteria identified was graded, and the types of bacteria seen were recorded. Nonfilamentous bacteria were categorized based upon Gram stain (positive or negative) and morphology (cocci or rods). Results. There were 11 females and 5 males. Nonfilamentous bacteria were identified in 16 of 16 (100%) specimens and filamentous bacteria were identified in 15 of 16 (94%) specimens. The mean percentage of filamentous bacteria relative to total bacteria was 57%. Regarding the nonfilamentous bacteria present, 69% of specimens had Gram-positive cocci only, 25% had Gram-positive and Gram-negative cocci, and 6% had Gram-positive cocci and Gram-positive rods. Conclusion. In the current study, there was a mix of filamentous and nonfilamentous bacteria in almost all canalicular concretions analyzed. Nonfilamentous bacteria may contribute to the pathogenesis of canaliculitis. In addition, the success of bacterial culture can be variable; therefore, pathological analysis can assist in determining the etiology.

1. Introduction

Canaliculitis is a relatively rare disorder which has classically been associated with Actinomyces species. The typical histology consists of microscopic granules with basophilic masses, an eosinophilic periphery, and a background of Gram-positive filamentous bacteria [13]. Repp and coworkers demonstrated that Actinomyces was identified on histopathology in nearly all canaliculitis concretion specimens, with infrequent identification of nonfilamentous bacteria [4]. Culture results have suggested that other Gram-positive and/or Gram-negative bacteria can be found in canaliculitis specimens [16]. Interestingly, a recent histopathological study by Perry and coworkers noted that Gram-positive cocci were “frequently seen colonizing the outer perimeter of the concretions,” although Actinomyces was the predominant organism [3]. Bacterial culture has variable success in this setting, and several studies have emphasized the utility of histopathological analysis for determining the bacterial composition of canalicular concretions [7, 8]. The purpose of this study was to determine the extent to which nonfilamentous bacteria colonize canalicular concretions by quantifying the types and proportions of bacteria present with graded histopathological analysis. This may assist in determining the etiology of canaliculitis.

2. Methods

A retrospective review was performed on all canalicular concretion specimens submitted for pathological analysis at Albany Medical Center between 2006 and 2013. The specimens were identified by searching the pathology database with the terms “canaliculitis” and/or “infectious granules.” Information was recorded from the pathology reports including eyelid involved, patient age, and gender. Institutional Review Board (IRB) approval was obtained for this study and it is compliant with the Health Insurance Portability and Accountability Act (HIPAA).

Canaliculitis specimens were obtained from patients through curettage or vertical canaliculotomy with retrograde expression of concretions [9]. All specimens were stained with hematoxylin and eosin (H&E) as well as Gomori’s methenamine silver (GMS) and Gram stains. The GMS stain facilitated identification of filamentous bacteria such as Actinomyces species and Gram stain was used for the identification of other bacteria. Concretions were initially identified at low power (100x) on H&E stain. The slides were analyzed to determine how many bacteria were present as well as types of bacteria that could be identified. Upon analysis, the total number of bacteria was first estimated. This was achieved by examining each slide at 400x magnification using a 10 mm by 10 mm grid reticle (total of 100 1 mm by 1 mm individual blocks). The average number of bacteria per individual block within the grid was recorded. The relative amount of bacteria in each specimen was categorized as none (0 per individual block), “low” (1–20), “medium” (21–40), or “high” (greater than 40).

Following this analysis, the types of bacteria present were determined using 200x and 400x magnification. The proportional amount of Gram-positive/GMS-positive filamentous bacteria (Actinomyces) present in each specimen was then graded as a percentile of the total bacteria identified. Percentages were recorded to the nearest 5%. Nonfilamentous bacteria were recorded as Gram-positive cocci, Gram-negative cocci, Gram-positive rods, and/or Gram-negative rods based upon their morphology and Gram stain characteristics.

The English medical literature was reviewed using the search terms “canaliculitis,” “canalicular concretions,” and “lacrimal concretions.”

3. Results

A total of 16 specimens from 16 patients were identified which met the criteria for canaliculitis concretions. There were 11 females and 5 males. The average patient age was 61 years (range 30 to 85 years). Table 1 outlines the demographic data and analysis for all 16 pathological specimens.

AgeGenderEyelidTotal bacterial count% Actinomyces within concretionsNonfilamentous bacteria identified

52MLULMedium90 Gram+ cocci
34FRLLLow0Gram+, gram− cocci
62FRLLHigh95Gram+ cocci
54FRLLMedium50Gram+ cocci
45MLLLMedium80Gram+, gram− cocci
69FLLLLow70Gram+ cocci
54FLLLMedium80Gram+ cocci
66MLLLLow40Gram+ cocci
78FRLLLow5Gram+ cocci
30FRLLLow50Gram+ cocci
45MLLLHigh50Gram+ cocci
65FRLLHigh95Gram+ cocci
75MLLLHigh80Gram+, gram− cocci
76FRLLLow20Gram+, gram− cocci
82FRLLMedium10Gram+ cocci, gram+ rods
85FRLLHigh95Gram+ cocci

Demographic and pathological analysis data for all specimens
M: male.
F: female.
RUL: right upper lid.
RLL: right lower lid.
LLL: left lower lid.

All of the specimens were found to consist of concretions on H&E stain, and all specimens contained at least some bacteria on Gram and GMS stains. When determining the grade for the total number of bacteria present in a given specimen, 6 (38%) were graded as “low,” 5 (31%) “medium,” and 5 (31%) “high.”

All 16 specimens had evidence of Gram-positive cocci; in 11 of 16 (69%) cases, the nonfilamentous bacteria were identified as Gram-positive cocci only; 4 of 16 (25%) specimens had Gram-positive and Gram-negative cocci; and 1 of 16 (6%) specimens had Gram-positive cocci and Gram-positive rods. Fifteen of sixteen specimens had filamentous bacteria. The mean percentage of filamentous bacteria relative to total bacteria was 57% (range 0 to 95%). In addition, all specimens demonstrated blue-staining bacteria surrounded by an eosinophilic fibrillary coat on H&E stain. Table 1 provides details on the percentage of filamentous bacteria and types of bacteria identified for all of the specimens analyzed. Figures 1(a) and 1(b) illustrate examples of the histopathological findings.

4. Discussion

Canaliculitis is a disease which is most commonly thought to be associated with yellow, gritty concretions secondary to Actinomyces species. As mentioned previously, the classic histopathology in Actinomyces-related infection reveals basophilic masses with an eosinophilic periphery and a background of Gram-positive, filamentous bacteria [13]. Other organisms have also been isolated through culture in cases of canaliculitis [2, 5, 6]. Several studies have reported that Staphylococcus species have been cultured from the expressed material in the canaliculus. Anand and coworkers and Vecsei and coworkers reported that Staphylococcus aureus was the most common organism identified and cultured in 26.6% and 25.3%, respectively, of patients with canaliculitis [5, 6]. Zaldivar and Bradley found that 21% of cultures grew Streptococcus and 13% grew Staphylococcus [10]. Although a number of bacteria have been cultured, the success of bacterial culture in the setting of canaliculitis can be somewhat variable. Previous studies have reported positive bacterial culture rates of 27% to 91% [7, 8]. In the current study, bacteria were readily identified on pathological analysis in all concretion specimens. Given the variability in culture results, histopathological analysis can be a useful adjunct in determining the etiology in these patients.

In a recent study using histopathologic evaluation, Perry and coworkers noted the presence of frequent Gram-positive cocci in canaliculitis concretions, although the dominant organism was reported to be Actinomyces species. The authors of this study commented that the Gram-positive cocci may contribute to the purulent nature of canaliculitis but felt that Actinomyces was the predominant etiologic agent leading to infection [3]. The results of our study, reported herein, demonstrated that a mixture of bacteria in canalicular concretions is quite common, being identified in all specimens analyzed. In addition, the current study grades the amount and types of bacteria present. On average, nonfilamentous bacteria were noted to be almost half of the organisms identified in concretions. Gram-positive cocci were noted in all specimens. In contrast to the study by Perry and coworkers, 25% of samples were also found to have Gram-negative bacteria [3].

Actinomyces are well known to form concretions. However, other Gram-negative and Gram-positive bacteria are also known to form concretions in other parts of the body, a finding sometimes referred to as “botryomycosis.” One of the main pathological characteristics of this finding is blue-staining bacteria surrounded by an eosinophilic fibrillary coat, known as the Splendore Hoeppli phenomenon [11, 12]. This specific finding was identified in all specimens of the current study. The diagnosis of botryomycosis is often unrecognized because it can appear similar to actinomycosis both clinically and histopathologically. The most common bacteria associated with this entity are Staphylococcus species [13, 14]. It is thought that the organisms form granules as a defense mechanism against the body’s immune system which allows them to promote the disease process. The prevalence of the Splendore Hoeppli phenomenon lends evidence to the presence of nonfilamentous bacteria in canaliculitis specimens, though the authors do not necessarily believe that it discounts the presence of Actinomyces. Both Actinomyces and nonfilamentous bacteria were found in the majority of specimens of this study, and it is plausible that they both contribute to the pathogenesis of canaliculitis. Additional research, such as polymerase chain reaction (PCR) study of canaliculitis specimens, could help to further elucidate the bacterial diversity in this disease.

Most of the nonfilamentous bacteria identified in the current study were Gram-positive cocci. Staphylococcus and Streptococcus species are included in this category and are the types identified most often by culture in prior studies [5, 6, 10]. Gram-negative cocci and Gram-positive rods were found as well, though less frequently. Previous culture studies from patients with canaliculitis have identified Haemophilus influenza, which can be seen as Gram-negative cocci, and Gram-positive rods such as Corynebacterium and Propionibacterium [2, 15]. Moraxella is another Gram-negative coccus which is known to cause other ocular infections such as keratitis [16]. In addition, Gram-negative organisms have been identified in normal conjunctiva and in chronic dacryocystitis. In one study, Gram-negative bacteria were found in 20% of dacryocystitis cultures [17, 18].

The demographic characteristics of the patients included in this study were similar to previous reports, with the lower eyelids being more commonly involved (15 of 16 eyelids), the subjects were primarily female, and the average age was 61 years [1922]. The limitations of this study include its retrospective nature and limited sample size. Also certain patient historical information, such as punctal plug placement, was not available for this study. This information could add additional information in determining the etiology of canaliculitis. While no claim is made of the superiority of histopathological analysis over bacterial culture for the evaluation of canaliculitis and associated concretions, pathological analysis can be a useful adjunct. The current study found that a mixture of bacteria (“mixed infection”) is often present in histopathologic sections of canalicular concretions and further revealed that a relatively large percentage of nonfilamentous bacteria (both Gram-positive and Gram-negative) can be seen on pathological analysis. These bacteria may contribute to the pathogenesis of canaliculitis.

Competing Interests

The authors declare that there are no competing interests regarding the publication of this paper.


  1. J. R. Brown, “Human actinomycosis. A study of 181 subjects,” Human Pathology, vol. 4, no. 3, pp. 319–330, 1973. View at: Publisher Site | Google Scholar
  2. J. R. Freedman, M. S. Markert, and A. J. Cohen, “Primary and secondary lacrimal canaliculitis: a review of literature,” Survey of Ophthalmology, vol. 56, no. 4, pp. 336–347, 2011. View at: Publisher Site | Google Scholar
  3. L. J. P. Perry, F. A. Jakobiec, and F. R. Zakka, “Bacterial and mucopeptide concretions of the lacrimal drainage system: an analysis of 30 cases,” Ophthalmic Plastic and Reconstructive Surgery, vol. 28, no. 2, pp. 126–133, 2012. View at: Publisher Site | Google Scholar
  4. D. J. Repp, C. N. Burkat, and M. J. Lucarelli, “Lacrimal excretory system concretions: canalicular and lacrimal sac,” Ophthalmology, vol. 116, no. 11, pp. 2230–2235, 2009. View at: Publisher Site | Google Scholar
  5. S. Anand, K. Hollingworth, V. Kumar, and S. Sandramouli, “Canaliculitis: the incidence of long-term epiphora following canaliculotomy,” Orbit, vol. 23, no. 1, pp. 19–26, 2004. View at: Publisher Site | Google Scholar
  6. V. P. Vecsei, V. Huber-Spitzy, E. Arocker-Mettinger, and F. J. Steinkogler, “Canaliculitis: difficulties in diagnosis, differential diagnosis and comparison between conservative and surgical treatment,” Ophthalmologica, vol. 208, no. 6, pp. 314–317, 1994. View at: Publisher Site | Google Scholar
  7. M. J. Lee, H.-K. Choung, N. J. Kim, and S. I. Khwarg, “One-snip punctoplasty and canalicular curettage through the punctum: a minimally invasive surgical procedure for primary canaliculitis,” Ophthalmology, vol. 116, no. 10, pp. 2027–2030.e2, 2009. View at: Publisher Site | Google Scholar
  8. S. Kaliki, M. J. Ali, S. G. Honavar, G. Chandrasekhar, and M. N. Naik, “Primary canaliculitis: clinical features, microbiological profile, and management outcome,” Ophthalmic Plastic and Reconstructive Surgery, vol. 28, no. 5, pp. 355–360, 2012. View at: Publisher Site | Google Scholar
  9. B. Perumal and D. R. Meyer, “Vertical canaliculotomy with retrograde expression of concretions for the treatment of canaliculitis,” Ophthalmic Plastic and Reconstructive Surgery, vol. 31, no. 2, pp. 119–121, 2015. View at: Publisher Site | Google Scholar
  10. R. A. Zaldivar and E. A. Bradley, “Primary canaliculitis,” Ophthalmic Plastic & Reconstructive Surgery, vol. 25, pp. 481–484, 2009. View at: Google Scholar
  11. P. Hacker, “Botryomycosis,” International Journal of Dermatology, vol. 22, no. 8, pp. 455–458, 1983. View at: Publisher Site | Google Scholar
  12. I. R. Toth and H. L. Kazal, “Botryomycosis in acquired immunodeficiency syndrome,” Archives of Pathology and Laboratory Medicine, vol. 111, no. 3, pp. 246–249, 1987. View at: Google Scholar
  13. C. Padilla-Desgarennes, D. Vázquez-González, and A. Bonifaz, “Botryomycosis,” Clinics in Dermatology, vol. 30, no. 4, pp. 397–402, 2012. View at: Publisher Site | Google Scholar
  14. J. W. Pruitt, S. R. Sabol, B. C. Fox, and M. S. Goldwasser, “Botryomycosis with orbital invasion: case report and literature review,” Journal of Oral and Maxillofacial Surgery, vol. 53, no. 5, pp. 599–605, 1995. View at: Publisher Site | Google Scholar
  15. S.-C. Lin, S.-C. Kao, C.-C. Tsai et al., “Clinical characteristics and factors associated the outcome of lacrimal canaliculitis,” Acta Ophthalmologica, vol. 89, no. 8, pp. 759–763, 2011. View at: Publisher Site | Google Scholar
  16. S. Das, M. Constantinou, M. Daniell, and H. R. Taylor, “Moraxella keratitis: predisposing factors and clinical review of 95 cases,” British Journal of Ophthalmology, vol. 90, no. 10, pp. 1236–1238, 2006. View at: Publisher Site | Google Scholar
  17. T. R. Singer, S. J. Isenberg, and L. Apt, “Conjunctival anaerobic and aerobic bacterial flora in paediatric versus adult subjects,” British Journal of Ophthalmology, vol. 72, no. 6, pp. 448–451, 1988. View at: Publisher Site | Google Scholar
  18. J. Hartikainen, O. Lehtonen, and K. Saari, “Bacteriology of lacrimal duct obstruction in adults,” British Journal of Ophthalmology, vol. 81, no. 1, pp. 37–40, 1997. View at: Publisher Site | Google Scholar
  19. A. J. Berlin, R. Rath, and L. Rich, “Lacrimal system dacryoliths,” Ophthalmic Surgery, vol. 11, no. 7, pp. 435–436, 1980. View at: Google Scholar
  20. E. Demant and J. J. Hurwitz, “Canaliculitis: review of 12 cases,” Canadian Journal of Ophthalmology, vol. 15, no. 2, pp. 73–75, 1980. View at: Google Scholar
  21. I. Hussain, R. E. Bonshek, K. Loudon, M. Armstrong, and A. B. Tullo, “Canalicular infection caused by actinomyces,” Eye, vol. 7, no. 4, pp. 542–544, 1993. View at: Publisher Site | Google Scholar
  22. M. A. Pavilack and B. R. Frueh, “Thorough curettage in the treatment of chronic canaliculitis,” Archives of Ophthalmology, vol. 110, no. 2, pp. 200–202, 1992. View at: Publisher Site | Google Scholar

Copyright © 2016 Balaji Perumal et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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