Trauma-induced filtering bleb formation and blebitis 40 years following a penetrating eye injury
- 1 Ophthalmology, Manchester University NHS Foundation Trust, Manchester, Greater Manchester, UK
- 2 Ophthalmology, East Lancashire Hospitals NHS Trust, Blackburn, Lancashire, UK
- Correspondence to Dr Yee Ling Wong; yeelingwong@nhs.net
Abstract
A 49-year-old man presented to the emergency eye clinic with a 3-week history of redness, irritation and blurred vision in his right eye, with a noticeable lesion superotemporally on the conjunctiva. He had a previous ocular history of penetrating glass injury in the right eye at the age of 9 years (40 years ago), of which no surgical intervention was performed at that time, as his parents did not seek medical attention. Slit lamp examination revealed a thin, conjunctival cystic bleb at 10 o’clock position with surrounding conjunctival injection and chemosis at close proximity to the site of previous ocular trauma. Investigations confirmed a diagnosis of trauma-induced filtering bleb with blebitis (bleb inflammation). The patient was treated with a combination of steroid and antibiotic drops for duration of 2 weeks. Subsequent follow-up revealed marked improvement of symptoms with reduced inflammation. Patient is being monitored regularly to prevent recurrence of blebitis and bleb associated complications.
Background
Although rare, spontaneous filtering bleb can cause sight threatening complications such as hypotonic disc swelling and maculopathy, bleb leakage and bleb-associated infections like blebitis and bleb-associated endophthalmitis.1 2 Early diagnosis and management is vital to prevent these sequelae. To our best knowledge, spontaneous filtering bleb is of rare occurrence and only a handful of cases have been reported until now. It is typically observed in patients with connective tissue disorders and patients with ocular abnormalities such as Axenfield syndrome and Terrien marginal degeneration.3 4 This report describes the management of a rare case of trauma-induced filtering bleb formation, who presented with a potentially sight-threatening blebitis 40 years after a penetrating eye injury.
Case presentation
A 49-year-old man presented with a 3-week history of redness, irritation and blurred vision in his right eye following a 2-week trip to the Canary Island, with a noticeable lesion superotemporally. He had a previous ocular history penetrating glass injury at the age of 9 (40 years ago) in the right eye, of which his parents did not seek any medical intervention. The patient describes being thrown a glass bottle while playing in the garden, leaving shattered glass in contact with his face. He suffered a superficial laceration of the right upper lid, which was padded by his parents. Best-corrected visual acuity at first presentation (BCVA) was 0.2 using LogMar visual acuity chart and intraocular pressure (IOP) was 9 mm Hg in the right eye and 12 mm Hg in the left eye. Slit lamp examination revealed a thin, pale, conjunctival cystic bleb at the superotemporal region at 10 o’clock position with surrounding conjunctival injection at close proximity to the site of previous ocular trauma. Examination findings also showed peaked iris pointing to the site of penetrating injury. The patient is systemically well with no history of connective-tissue disorder.
Investigations
Gonioscopy of the superotemporal angle shows slight narrowing of the superotemporal angle. Anterior segment optical coherence tomography (AS-OCT) documented the presence of a filtering bleb with patent sclerostomy (figure 1). Macular optical coherence tomography (M-OCT) was unremarkable with no evidence of maculopathy or signs of hypotony such as choroidal folds. Siedel test was done to rule out any leakage of aqueous from the filtering bleb. Slit lamp examination showed no evidence of peripheral corneal or limbal thinning. Ocular ultrasonography (USG) of the posterior segment was unremarkable.
AS-OCT showing cross-section of spontaneous pseudobleb formation. AS-OCT, anterior segment optical coherence tomography.

Treatment
In the absence of bleb leakage and vitreous involvement, the patient was treated aggressively with topical ofloxacin 0.3% (PL 00426/0070) six times a day and topical prednisolone 1% (PL 00426/0051) four times daily. Mydrilate 1% (PL 17509/0008) eye drops was also prescribed three times a day to ensure patient comfort. The patient was reviewed on a daily basis until clinical improvement was noted.
Outcome and follow-up
Follow-up reveals symptomatic relief and complete resolution of blebitis. The patient continues to be monitored at a 4 monthly intervals with good BCVA and well-controlled IOP.
Discussion
To our best knowledge, spontaneous filtering bleb is of rare occurrence and only a handful of cases have been reported to date. It is typically observed in patients with connective tissue disorders and patients with ocular abnormalities such as Axenfeld syndrome and Terrien marginal degeneration.3 4 Nemet et al reported the first case in a patient with Axenfeld syndrome postulating raised IOP as a causative factor of rupture of corneoscleral junction with subsequent formation of filtering bleb.3 5 Diseases of the peripheral cornea such as Terrien and Pellucid marginal degeneration resulting in rupture of the Descemet’s membrane are also known causes of spontaneous bleb formation.3 4 Khouri et al described a traumatic cause of filtering bleb many years after penetrating glass injury to the eye, with an apparent posterior communicating channel between the bleb and cilliary body on ultrasound biomicroscopy.6 This case is interestingly very similar to ours, except that our patient presented with blebitis—a potential complication of bleb formation (both spontaneous and surgical).
Blebitis was first described in 1994 as presumed infection of a filtering bleb with minimal or no anterior chamber reaction without vitreous involvement.7 According to Shaarawy and colleagues, the mechanisms causing blebitis remain largely unknown. In an early-onset bleb-related infection following a glaucoma filtration surgery, pathogens are likely to be introduced perioperatively or during the early postoperative period. The pathogenesis in a late-onset bleb-related infection is more likely associated with the barrier functions (both physical and immunological) of the conjunctiva and the virulence of invading organism. In this case, the patient developed blebitis during his 2-week vacation in a high ultraviolet (UV) environment which could have potentially suppressed his immune system causing invasion and proliferation of microorganism in this vulnerable area.8 Risk factors of increased bleb-related infections include bleb leak, recurrent blepharitis, conjunctivitis, ocular surface disease, inferior or nasal bleb and thin, cystic bleb. Younger age, male, diabetes, malnutrition and poor immune system are also important risk factors.2 8 9 In our case, the location of the thin cystic bleb was between 9 o’clock and 11 o’clock position however most surgical blebs are located between the 11 o’clock and 1 o’clock position. Surgical bleb also differ from traumatic bleb as they have a partial thickness scleral flap. Early diagnosis and management is vital with aggressive topical treatment targeting common pathogens in blebitis like Staphylococcus aureus and Staphylococcus epidermidis. Options include fluoroquinolones or fortified topical antibiotics such as vancomycin or cefazolin in combination with an aminoglycoside. A randomised control trial published by Cantor et al reported that topical levofloxacin provide better aqueous penetration compared with ofloxacin and ciprofloxacin eye drops in eyes with functioning filtering bleb.10 Nonetheless, our patient responded well with topical ofloxacin monotherapy. We also prescribed topical cyclopegic (mydrilate 1%) as a supportive measure to relieve pain and to prevent anterior-segment inflammation-related posterior synaechiae.11 Although there is no standard treatment regime of blebitis among glaucoma consultants, successful treatment will ensure good visual outcome. However if left untreated, blebitis may lead to bleb-associated endophthalmitis manifesting with severe pain, markedly reduced vision and vitreous inflammation.2 The use of prophylactic antibiotics is not recommended, but the management of ocular surface disease may play a key role in enhancing conjunctival resistance.8
Although our patient has been asymptomatic without bleb dysesthesia and with good IOP control, patients with filtering conjunctival bleb should be routinely observed to look for blebitis and bleb-associated infections. Disruption of globe integrity can cause bleb leak resulting in low IOP. This can subsequently cause hypotony maculopathy when IOP reduces to 4 mm Hg and below thereby affecting vision. Should this occur, dehiscence of old scleral scars can be repaired by tightly suturing the sclera, or by using amnion membrane, conjunctival rotation flap or scleral patch.12 Therefore, ultrasound biomicroscopy should be performed and documented for surgical planning if repair becomes necessary.6
Learning points
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Spontaneous filtering bleb formation with first presentation of blebitis is a rare finding and have not previously been reported in literature.
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History taking especially previous ophthalmic history is vital to tease out the diagnosis.
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Timely recognition and intervention of spontaneous filtering bleb is important to prevent sight-threatening complications.
Acknowledgments
I would like to thank Hanif Patel (Senior Ophthalmic & Vision Science Practitioner) for the AS-OCT images.
Footnotes
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Contributors YLW was involved in first draft of manuscript. VS was involved in revising and critically appraising manuscript.
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Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
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Competing interests None declared.
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Patient consent for publication Obtained.
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Provenance and peer review Not commissioned; externally peer reviewed.
- © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.
References
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