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CASE REPORT
Necrotizing Pseudomonas
Blepharoconjunctivitis
Edward H. Hughes
Department of ophthalmology,
Princess Royal University
Hospital, Farnborough,
Kent, UK
Riaz I. Ahmed
Department of paediatrics,
Princess Royal University
Hospital, Farnborough,
Kent, UK
Christopher J. Hammond
Department of ophthalmology,
Princess Royal University
Hospital, Farnborough,
Kent, UK
INTRODUCTION
Necrotizing Pseudomonas blepharoconjuctivitis is an extremely rare condition
with potentially severe complications and resistance to treatment with many
antibacterials used for pre-septal cellulitis. We describe a case of a 20-month-old
female infant with a necrotizing eyelid infection caused by P. aeruginosa.
CASE REPORT
A 20-month-old girl was admitted to hospital with a 3-day history of a sticky
right eye with progressive eyelid swelling. She was previously well but on the day
of admission was listless and pyrexial (39.9 C). Examination revealed erythema
and swelling of the right lower eyelid, mild conjunctival injection and a clear
cornea. Ocular movements were full and there was no proptosis. A diagnosis of
pre-septal cellulitis was made, conjunctival swabs were taken and she was commenced on topical chloramphenicol and a second generation cephalosporin
antibiotic intravenously. This was changed after one dose to piptazobactam
and gentamicin in line with a febrile neutropenia protocol when the result
of her full blood count revealed a leukocyte count of 22.3 109 /L with 73%
lymphoblasts. She was anaemic (Hb 8.2 g/dl), thrombocytopenic (platelets
34 109 /L) and neutropenic (0.7 109 /L). A provisional diagnosis of acute
lymphoblastic leukaemia was made and was later confirmed by a bone marrow
biopsy to be the common type.
The following day her pyrexia had improved and the lid swelling was unchanged, but there was some dark discolouration of the medial right lower lid
margin. Blood cultures were negative but conjunctival swab cultures had a heavy
growth of Pseudomonas aeruginosa resistant to second generation cephalosporins
but sensitive to ciprofloxacin and gentamicin. Ofloxacin drops were applied two
hourly and steady clinical improvement ensued, but the medial lower lid margin
became ulcerated and excavated, without eschar or devitalised tissue (Fig. 1).
Intravenous gentamicin was continued for two weeks and she was commenced on vincristine and dexamethasone according to the UKALL 2003
47
FIGURE 1 Photograph taken three days after commencing intravenous antibiotics showing mild residual swelling of the right
lower eyelid. An ulcerated notch deformity is seen medially involving the lacrimal punctum and there is loss of eyelashes from the
entire medial half of the lower lid.
protocol for first phase remission induction. The ulcerated area healed with conservative management leaving
a notch and at no point was the cornea involved.
DISCUSSION
Necrotizing
blepharoconjunctivitis
due
to
Pseudomonas aeruginosa infection is an extremely
rare but potentially devastating complication of a
compromised immune status. This Gram-negative rod
is a common ocular pathogen found in microbial
keratitis (Varaprasathan et al., 2004) (often secondary
to contact lens wear), in outbreaks of conjunctivitis on
neonatal intensive care units (Shah & Gallagher, 1998),
and may occasionally cause infection in the presence
of a foreign body (e.g. scleral buckle (Chaudhry et al.,
1998)), as well as infections at other sites including
the skin and lower respiratory tract. Certain strains of
the bacterium are known to produce a range of lytic
enzymes, including elastase and proteases (Morihara
& Tsuzuki, 1977), which enhance its invasiveness,
and although healthy humans are highly resistant to
invasion by Pseudomonas aeruginosa at vascularised
sites, infection of the avascular cornea may result in
perforation and profound visual consequences. Invasive infection of the conjunctiva and eyelid probably
requires significant immune compromise since this
complication has only been described previously in
three individuals (Giagounidis et al., 1997; Rosenoff
et al., 1974; Steinkogler & Huber-Spitzy, 1988), two
E. H. Hughes et al.
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