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Author: Manolette R Roque, MD, MBA, DPBO, FPAO, President and CEO, Chief of Service, Ocular Immunology and Uveitis, Consulting Staff, Cornea and Refractive Surgery, Eye Republic Ophthalmology Clinic; General Manager, Ophthalmic Consultants Philippines Co; Consulting Staff, CME Liaison, Section Chief of Ocular Immunology and Uveitis, Department of Ophthalmology, Asian Hospital and Medical Center

Manolette R Roque, MD, MBA, DPBO, FPAO, is a member of the following medical societies: American Academy of Ophthalmic Executives, American Society of Cataract and Refractive Surgery, American Society of Ophthalmic Administrators, American Uveitis Society, International Ocular Inflammation Society, Philippine Medical Association, Philippine Ocular Inflammation Society, and Philippine Society of Cataract and Refractive Surgery

Coauthor(s): Barbara L Roque, MD, Full Partner, Ophthalmic Consultants Philippines Co, Chief of Service, Pediatric Ophthalmology and Strabismus, Consulting Staff, Orbit and Eye Plastics, EYE REPUBLIC Ophthalmology Clinic; C Stephen Foster, MD, FACS, FACR, FAAO, Clinical Professor of Ophthalmology, Harvard Medical School; Consulting Staff, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary; Founder and President, Ocular Immunology and Uveitis Foundation, Massachusetts Eye Research and Surgery Institution

Editors: Jorge G Camara, MD, Chairman, Department of Ophthalmology and Otorhinolaryngology, Director of Fellowship Training Program, St Francis Medical Center; Associate Professor, Department of Surgery, University of Hawaii School of Medicine; Donald S Fong, MD, MPH, Assistant Clinical Professor of Ophthalmology, Director, Clinical Trials Research, Department of Ophthalmology, Southern California Permanente Medical Group; Mark T Duffy, MD, PhD, Consulting Staff, Division of Oculoplastic, Orbito-facial, Lacrimal, and Reconstructive Surgery, Green Bay Eye Clinic, BayCare Clinic; Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri; Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences

Author and Editor Disclosure

Synonyms and related keywords: Actinomycetales, Actinomycetaceae, Actinomycetes, Actinomyces, Actinomyces israelii, A israelii, keratoactinomycosis, keratitis, canaliculitis, anaerobic bacillus

Background

The bacterial order Actinomycetales comprises 3 families: Actinomycetaceae, Mycobacteriaceae, and Streptomycetaceae. Genus Actinomyces, a member of the family Actinomycetaceae, grows as a fragile branching filament that tends to fragment into bacillary and coccoid forms producing chains of either conidia or arthrospores.

Actinomyces israelii species is a gram-positive, cast-forming, non–acid-fast, non–spore-forming anaerobic bacillus that is difficult to isolate and identify. Its filamentous growth and mycelialike colonies have a striking resemblance to fungi. They are soil organisms, often found in decaying organic matter (eg, wet hay, straw). It is primarily a commensal microbe found in normal oral cavities, in tonsillar crypts, in dental plaques, and in carious teeth.

Pathophysiology

Keratitis

Most reported cases of Actinomyces keratitis (keratoactinomycosis) are caused by A israelii. It is characterized by a dry ulceration with central necrosis, surrounded by a gutter of demarcation, usually accompanied by iritis and hypopyon. In severe cases, descemetocele and perforation may occur.

A primary corneal ulcer attributable to Actinomyces species is rare and usually follows corneal trauma. A rare case of keratoactinomycosis developing in the absence of any known ocular trauma was reported in Kuala Lumpur.

Canaliculitis

Primary chronic canaliculitis is an uncommon problem caused by A israelii (Streptothrix). McKellar presented a 10-year-old girl with a 6-month history of intermittent conjunctivitis and discharge from her pouted left lower punctum. Topical treatment with chloramphenicol/polymyxin sulphate failed despite a diagnosis of probable A israelii infection confirmed by microbiology. Surgical exploration revealed a canalicular diverticulum and 3 canaliculiths demonstrating solid casts of Actinomycetes on histologic examination. A therapeutic triad of punctoplasty, cast removal, and adjunctive topical cefazolin resulted in resolution.

Other ocular involvement

Actinomycetes have been described as causative organisms in conjunctivitis, blepharitis, dacryocystitis, postsurgical endophthalmitis, and infected porous orbital implant. Cervico-facial actinomycosis has also been reported.

Endophthalmitis, attributable to Actinomyces viscosus, developed in a 78-year-old man after cataract surgery. Postoperative endophthalmitis with this organism is a rare occurrence. Inflammation was characterized by anterior segment and vitreous cellular debris in cases of chronic postoperative endophthalmitis associated with Actinomyces species.

Frequency

United States

Primary chronic canaliculitis is an uncommon problem that can be overlooked; however, it may account for approximately 2% of all tearing problems. Actinomycosis may form in up to 2% of all lacrimal disease. Its occurrence is probably much less in other areas.

Race

No racial predilection exists.

Sex

No sexual predisposition exists.

Age

No age predisposition exists.



History

  • Keratitis
    • Symptoms
      • Progressive visual haze
      • Increasing ocular pain
      • Photophobia
      • Constant watering
      • Redness
    • Past ocular history
      • Corneal trauma, especially when contaminated by vegetable matter
      • Ongoing, nonresponsive treatment
    • Personal history - Outdoor laborer
  • Canaliculitis
    • Symptoms
      • Chronic or recurrent conjunctivitis
      • Chronic mucopurulent discharge
      • Epiphora
      • Ocular surface irritation
      • Medial eyelid and canthal pain
      • Pouting punctum
      • Failure to resolve despite topical treatment
    • Past ocular and medical history similar to keratitis

Physical

  • Keratitis
    • Gross observations
      • Some conjunctival congestion
      • Gray-white corneal lesion
    • Slit lamp findings
      • A dry ulceration with central necrosis, surrounded by a gutter of demarcation, usually accompanied by iritis and hypopyon may be present.
      • Gray-white satellite stromal infiltrates adjacent to advancing edges may be present.
      • In severe cases, descemetocele and perforation may occur.
  • Canaliculitis
    • Gross observations
      • Chronic discharge, swollen and pouted punctum
      • A pouted punctum is clinically diagnostic, although it occurs in less than 50% of all patients who are affected.
      • Typically, the discharge is particulate and contains concretions.
      • The plica may be swollen and congested, and canalicular swelling and overlying lid erythema are often present.
      • The lower lid is more commonly affected, and the lacrimal sac and the duct are usually not involved.
    • Slit lamp findings
      • Pouted punctum
      • Plica may be swollen and congested.
      • Particulate canalicular discharge with or without concretions

Causes



Blepharitis, Adult
Cellulitis, Preseptal
Chalazion
Conjunctivitis, Bacterial
Contact Lens Complications
Dacryocystitis
Endophthalmitis, Fungal
Endophthalmitis, Postoperative
Keratitis, Fungal
Nasolacrimal Duct, Obstruction
Ulcer, Corneal

Other Problems to be Considered

Propionibacterium propionicus canaliculitis
Candida species canaliculitis



Lab Studies

  • Canalicular discharge and canaliculiths may be sent for the following studies:
    • Gram stain/Giemsa stain
    • Cultures and sensitivities (ie, blood agar, Sabouraud, anaerobic)
    • Special stains (ie, calcofluor white)

Imaging Studies

  • Distension dacryocystography: Contrast material is used to visualize the anatomic details of the lacrimal drainage system.
  • Scanning electron microscopy
  • High-resolution ultrasound (transducer frequency of 20 MHz): The 20-MHz scanner images may reveal pathological findings that are invisible during a slit lamp examination. Ultrasonic images of chronic canaliculitis show ectasia of the canaliculus and sulfur grains measuring 1-2 mm in diameter.

Other Tests

  • Probing may be performed with a lacrimal probe to check for a diverticulum and remaining casts.

Procedures

  • Perform a 2-snip punctoplasty under anesthesia.
  • Curettage may also be helpful in removing any adherent casts from the canaliculus.
  • Subsequent lacrimal irrigation with 2 MU of penicillin in 20 mL of sterile water may be helpful.

Histologic Findings

Histologic examination of the canaliculiths demonstrated that they consisted of solid casts of Actinomycetes with typical branching and filamentous structures. The organisms were found by using a Gram stain on the histopathologic preparations and by using a scanning electron microscopy.

Electron microscopic results of an actinomycosis of the lacrimal canaliculus were presented in 1980. The interior of the actinomycotic conglomerate showed no evidence of a cellular defense reaction, but, in the loosely woven outer network of hyphae, a massive granulocytic reaction was observed to be present. After phagocytosis, the structure of the actinomycotic microorganisms within the granulocytes was not significantly damaged. Within the tissue of the lacrimal canaliculus, adjacent to the actinomycotic conglomerate, an increased number of plasma cells were observed to be present; however, no organisms were present.



Medical Care

  • Keratitis: Actinomycetes are usually susceptible to penicillins and cephalosporins. The treatment of keratoactinomycosis used to be excision of necrotic tissue, followed by cauterization. However, good results have been obtained by subconjunctival penicillin coadministered with systemic iodides. Alternatively, topical sulfacetamide or penicillin can be used.
  • Canaliculitis: Actinomycetes are usually susceptible to penicillins and cephalosporins. Postoperatively, patients may be treated with topical cefazolin for 1 month. Adjunctive hyperbaric oxygen therapy for actinomycotic lacrimal canaliculitis has been reported.

Surgical Care

  • Keratitis: All reported cases of keratoactinomycosis responded to therapy, which included intraocular, topical, and systemic antibiotics, as well as pars plana vitrectomy and partial iridectomy. Urgent keratoplasty for a corneal infection by Actinomyces species was reported in a 41-year-old man.
  • Canaliculitis: Failure to resolve canaliculitis by using topical treatment requires surgical exploration of the canalicular system and removal of any casts. Extensive surgery is not always required. A 2-snip punctoplasty, cast removal, curettage, probing, and adjunctive antibiotic therapy usually result in resolution of the canaliculitis. Cultivation of the surgically obtained dacryoliths and secretion enables reliable proof of Actinomyces and allows for an appropriate therapy for canaliculitis. Even though Actinomyces is sensitive to penicillin, cure of canaliculitis does not occur until all the concretions and the granulations that are present in the canaliculus are meticulously removed.

Consultations

An oculoplastics consult may be required.



Actinomyces organisms are usually susceptible to penicillins and cephalosporins. Good results have been obtained by subconjunctival penicillin coadministered with systemic iodides. Alternatively, topical sulfacetamide or penicillin can be used.

Drug Category: Antibiotics

Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.

Drug NamePenicillin G (Pfizerpen)
DescriptionExerts bactericidal action against penicillin-susceptible microorganisms during the stage of active multiplication. Acts by inhibiting biosynthesis of cell wall mucopeptide, rendering the cell wall osmotically unstable. Not active against penicillinase-producing bacteria, which include many strains of staphylococci
Adult DoseTopical: 100,000-333,000 U/mL in topical
Subconjunctival: 0.5-1.0 million U/mL
Intravitreal: 2,000 U and probenecid 0.5 g PO qid (possible retinal toxicity)
Oral: 400,000 U PO qid (rarely used; poor stomach absorption)
IV: 2-6 million U IV q4h and probenecid 0.5 g PO qid
IM: Depends on formulation
Pediatric DoseTopical: 10,000-20,000 U/mL
IV: 50,000 U/kg/d IV divided bid/tid
ContraindicationsDocumented hypersensitivity
InteractionsProbenecid can increase effects; coadministration of tetracyclines can decrease effects
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsCaution in impaired renal function

Drug NameCefazolin (Ancef, Kefzol, Zolicef)
DescriptionFirst-generation cephalosporin with excellent activity against gram-positive cocci, including penicillinase-producing Staphylococcus aureus, penicillinase-producing Staphylococcus epidermidis, group A beta-hemolytic streptococci (Streptococcus pyogenes), group B streptococci (Streptococcus agalactiae), and Streptococcus pneumoniae. Ineffective against Bacteroides fragilis and only weak activity against gram-negative organisms.
Adult DoseTopical: 133 mg/mL
Subconjunctival: 100 mg/mL
Intravitreal: 2.25 mg plus probenecid 0.5 g PO qid
IV/IM: 500-1,000 mg IV/IM q6h
Pediatric Dose25-100 mg/kg/d IV/IM divided q6-8h depending on severity of infection; not to exceed 6 g/d
ContraindicationsDocumented hypersensitivity
InteractionsProbenecid can increase effects of penicillin; coadministration of tetracyclines can decrease effects of penicillin
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsProlonged use may result in overgrowth of nonsusceptible organisms; caution in GI disease, particularly colitis

Drug Category: Antiparasitic agents

Parasite biochemical pathways are sufficiently different from the human host to allow selective interference by chemotherapeutic agents in relatively small doses.

Drug NameSulfacetamide sodium 10% (Sulamyd, Bleph-10)
DescriptionN-acetyl-substituted derivative; at 30% solution, topical sulfacetamide has pH of 7.4 and has good tissue penetration.
Adult DoseSolution: Instill 1-3 gtt in affected eye q2-3h, while awake, with less frequent administration at night
Ointment: Apply 0.5-inch ribbon into the conjunctival sac 1-4 times/d
Pediatric Dose<2 months: Not established
>2 months: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsEffects of sulfonylurea hypoglycemic agents, hydantoin anticonvulsants, and oral anticoagulants increase when administered concurrently with sulfacetamide sodium; PABA antagonizes effects of sulfonamides; PABA esters (eg, procaine) may inhibit antibacterial effect of these agents; trimethoprim enhances effects of sulfacetamide
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in severely dry eye; ointment may retard corneal epithelial healing; if inflammation or pain persists >48 h or becomes aggravated, reevaluate therapy; adverse effects include local irritation, brow ache, blurred vision, transient burning and stinging, and sensitivity reactions (rare cases of Stevens-Johnson syndrome and exfoliative dermatitis have been reported); GI upset and bone marrow depression have been described



Further Outpatient Care

  • Patients should receive follow-up care as needed.

In/Out Patient Meds

  • Postoperatively, patients may be treated with topical cefazolin for 1 month.

Prognosis

  • Prognosis is excellent once the organism is positively identified and appropriately treated.

Patient Education

  • Patients should be advised to wear protective eye gear when working with vegetable matter.



Medical/Legal Pitfalls

  • Failure to properly identify the organism with subsequent appropriate medical and surgical management may lead to a persistent epiphora; intermittent, mucopurulent discharge; and a localized, tumorlike swelling on the involved site.

Special Concerns

  • While performing this work, the author was a Fellow and affiliated with the Ocular Immunology and Uveitis Service, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School.



Media file 1:  Canaliculitis of the left lower lid. Courtesy of Peter Rubin, MD, Director, Eye Plastics Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School.
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Media type:  Photo

Media file 2:  Canaliculitis of the right upper lid. Courtesy of Peter Rubin, MD, Director, Eye Plastics Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School.
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Media type:  Photo

Media file 3:  A pediatric patient with canaliculitis. Courtesy of Peter Rubin, MD, Director, Eye Plastics Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School.
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Media type:  Photo

Media file 4:  A patient presenting with pseudocanaliculitis secondary to a chalazion. Courtesy of Peter Rubin, MD, Director, Eye Plastics Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School.
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Media type:  Photo

Media file 5:  A patient presenting with pseudocanaliculitis secondary to a chalazion. Courtesy of Peter Rubin, MD, Director, Eye Plastics Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 6:  Actinomyces israelii (non–spore-forming, gram-positive bacilli). Courtesy of Medical Education Information Center, Department of Pathology and Laboratory Medicine, The University of Texas-Houston Medical School.
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Media type:  Image

Media file 7:  Actinomyces israelii. (The photo is labeled.)
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Media type:  Image

Media file 8:  Actinomycosis.
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Media type:  Image



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Actinomycosis excerpt

Article Last Updated: Mar 16, 2005