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Journal of Clinical Microbiology, July 2001, p. 2742-2744, Vol. 39, No. 7
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.7.2742-2744.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Endophthalmitis Caused by Listeria
monocytogenes
Carmen
Betriu,1,*
Santos
Fuentemilla,2
Rosalía
Méndez,2
Juan J.
Picazo,1 and
Julián
García-Sánchez2
Department of Clinical
Microbiology1 and Department of
Ophthalmology,2 Hospital Clínico San
Carlos, 28040 Madrid, Spain
Received 20 December 2000/Returned for modification 14 March
2001/Accepted 23 April 2001
 |
ABSTRACT |
Listeria monocytogenes was isolated from the aqueous
chamber of an immunodepressed patient with acute hypertensive uveitis, who developed a dark hypopyon and pigment dispersion. No extraocular septic focus was found. Treatment was successful with intravitreal vancomycin, anterior chamber irrigation with vancomycin, orally administered ciprofloxacin, and topical fortified vancomycin.
 |
CASE REPORT |
A 62-year-old man presented to the emergency
department with pain, redness, and decreased vision in the left eye.
The patient had a history of laryngeal carcinoma, for which he had
undergone laryngectomy and had been treated with radiation therapy and
steroids. Examination of the eye on admission revealed acute
hypertensive uveitis, and treatment with corticosteroids was begun but
did not provide significant improvement. The patient developed a dark hypopyon with pigment dispersion and uveal ectropion. A differential diagnosis was made between endogenous endophthalmitis and a neoplastic process of the ciliary body (either primary ciliary body melanoma or
metastatic melanoma from larynx carcinoma). Results from laboratory studies were unremarkable, except for the leukocyte count
(14,030/mm3 with 77% polymorphonuclear neutrophils). The
chest X ray was normal. Blood cultures were negative. An ultrasound
scan of the eye showed dispersion of echoes, and no evidence of retinal
detachment was noted. B-scan ultrasonography revealed inflammatory
deposition and pigmentary epithelium detachment. No proliferation was
detected in the stromal iris.
Anterior chamber paracentesis was performed and submitted for culture
and histopathology. Cytological examination showed polymorphonuclear leukocytes and no evidence of neoplastic cells. Because the patient reported a history of penicillin allergy, combined treatment with oral
administration of ciprofloxacin (750 mg twice a day), anterior chamber
irrigation with vancomycin, and intravitreal vancomycin (1 mg) was
started. Topical fortified vancomycin (1 g) and corticotherapy were
also applied. The patient's condition improved with treatment. Within
7 days, the hypopyon disappeared and the intraocular pressure decreased. However, visual acuity was limited to appreciation of hand
motion, because of a severe corneal edema and a cataract which
developed in the patient's left eye.
A small amount of fluid obtained by aspiration from the anterior
chamber was directly plated onto blood agar and chocolate agar and
distributed into aerobic and anaerobic blood culture bottles processed
by the BACTEC 9050 system (Becton Dickinson Microbiology Systems,
Cockeysville, Md.). Gram staining was performed and no organisms
were observed. After a 24-h incubation of plates at 35°C in a 5%
CO2-enriched atmosphere, catalase-positive, gram-positive coccobacilli grew, producing beta-hemolysis on blood agar. The isolate
was identified as Listeria monocytogenes by both the Wider system (Francisco Soria Melguizo, S.A., Madrid, Spain) and the API
Listeria system (bioMérieux, Marcy l'Etoile, France). Pure culture of L. monocytogenes was also isolated from both
aerobic and anaerobic bottles that were positive after 24 h of
incubation. Antibiotic susceptibility was determined in accordance with
the recommendations of the National Committee for Clinical Laboratory Standards (23) using a broth microdilution
procedure (Sensititre; Radiometer, Copenhagen, Denmark) with
cation-adjusted Mueller-Hinton broth with 5% lysed horse blood. The
MICs were as follows: penicillin, 0.12 µg/ml; ampicillin,
0.5
µg/ml; chloramphenicol, 4 µg/ml; vancomycin, 1 µg/ml;
ciprofloxacin, 1 µg/ml; rifampin,
1 µg/ml; trimethoprim-sulfamethoxazole,
0.5 µg/ml; tetracycline,
2
µg/ml; gentamicin,
4 µg/ml; and cefotaxime,
8
µg/ml.
L. monocytogenes is a ubiquitous gram-positive
bacillus. Its sources include sewage, silage, soil, and animals
(28). It causes several illnesses in humans, such as
meningitis or septicemia. Other reported forms of disease include
endocarditis, abortion, wound infection, pneumonia, encephalitis, and
ocular infections (24). Most L. monocytogenes
infections are sporadic, although during the last few decades several
outbreaks have been described (3, 9, 10, 18, 21).
Food-borne transmission has been demonstrated both in epidemic and
sporadic human listeriosis. A variety of foodstuffs have been
associated with listeriosis, including soft cheeses, raw vegetables,
fish, meat, and milk. It is now established that listeriosis can
present as a gastrointestinal disease with fever (3).
Although L. monocytogenes infections most frequently affect
neonates, pregnant women, immunosuppressed patients, those receiving
corticosteroids, and elderly patients, infection can also occur in
previously healthy persons.
Ocular listeriosis is rare, with conjunctivitis being the most frequent
manifestation. Keratitis, endophthalmitis, and acute chorioretinitis
have also been reported. Infective endophthalmitis is a potentially
devastating disease that may lead to loss of vision. Exogenous
endophthalmitis occurs after ocular surgery or penetrating ocular
trauma. Endogenous endophthalmitis results from the hematogenous spread
of bacterial infection to the eye. It is a rare entity that accounts
for 2 to 8% of all cases of endophthalmitis. Immunocompromised states,
chronic diseases such as diabetes mellitus or renal
insufficiency, malignancies, and intravenous drug use have been
reported in association with this disease (16, 26).
Greenwald et al. (16) reviewed 72 cases of metastatic
endophthalmitis published from 1976 to 1985, and found Bacillus
cereus as the most frequently reported species (15.3%), followed
by Neisseria meningitidis (11.1%) and Staphylococcus aureus and Haemophilus influenzae (each, 9.7%).
Gram-negative microorganisms, including Pseudomonas
aeruginosa and Enterobacteriaceae, accounted for 25%
of isolates. Three cases (4.2%) of endogenous endophthalmitis by
L. monocytogenes were included in the study. Later, in 1994, Okada et al. (26) reported, from a series of 28 patients
with endogenous endophthalmitis, 71% of cases due to gram-positive
organisms with streptococci and S. aureus accounting for 32 and 25% of all isolates, respectively. They found the endocardium to
be the most frequent source of infection, followed by the
gastrointestinal tract and the genitourinary tract. As endophthalmitis
is a severe, vision-threatening infection, early diagnosis and prompt
initiation of antibiotic therapy are essential. Therefore, the
condition warrants puncture of the anterior chamber or vitreous tap to
investigate the etiologic agent and a simultaneous intravitreous
antibiotic injection, as well as an intensive intravenous antibiotic administration.
L. monocytogenes is a rare cause of endophthalmitis. Since
the first case of endophthalmitis due to L. monocytogenes
reported by Goodner and Okumoto (15) in 1967, to our
knowledge, only 16 other cases have been published in the literature
(1, 2, 4-8, 12-14, 17, 19, 20, 22, 25, 29). Almost all
cases showed similar clinical features including decreased vision,
elevated intraocular pressure, and fibrinous anterior chamber reaction. Several patients developed a dark hypopyon. In all cases the cause of
bacterial endophthalmitis was determined by recovering the organism
from cultures of intraocular fluids. Six of the 17 published cases of
L. monocytogenes endophthalmitis occurred in
immunocompromised patients (2, 5, 7, 20, 22, 25), 6 occurred in elderly patients with good physical health (1, 4, 14,
15, 17, 19), and the remaining 5 cases affected young healthy
individuals (6, 8, 12, 13, 29). Our patient had several
potentially predisposing factors, including laryngeal carcinoma and
immunosuppressive therapy. An exogenous source of infection was not
identified in any of the reported cases. The present case was not
related to surgical procedures or to local trauma, and there was no
evidence of a distant focus of infection from which hematogenous spread occurred. Considering that the digestive tract is a likely route of
entry of L. monocytogenes, we suggest that the organism
might have entered the body orally, disrupted the mucosal barriers, and
invaded the eye via the bloodstream.
L. monocytogenes is susceptible to a wide range of
antibiotics but not to cephalosporins. Nevertheless, since the
isolation of the first multiresistant strain of L. monocytogenes in France in 1988 (27), strains
resistant to one or several antibiotics, such as trimethoprim,
erythromycin, streptomycin, tetracycline, or chloramphenicol, have
become more frequent (11). The treatment of choice for
systemic L. monocytogenes infection is the administration of
ampicillin or penicillin G combined with an aminoglycoside such as
gentamicin. Trimethoprim-sulfamethoxazole alone or with rifampin is
considered an alternative treatment for patients who are allergic to
penicillin. For our isolate, MICs of almost all antibiotics tested,
including ciprofloxacin, were low. To our knowledge, this is the first
case of L. monocytogenes endophthalmitis which has been
treated with oral ciprofloxacin combined with intravitreal and topical vancomycin.
This paper points out the importance of prompt and accurate
identification of the infectious agent by the microbiologist in the
management of endophthalmitis. Although endophthalmitis due to L. monocytogenes is uncommon, the possible presence of this entity
should be kept in mind regardless of the age or immunological status of
the patient.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Department of
Clinical Microbiology, Hospital Clínico San Carlos, Plaza
Cristo Rey s/n, 28040 Madrid, Spain. Phone: 34 913303486. Fax: 34 913303478. E-mail: cbetriu{at}efd.net.
 |
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Journal of Clinical Microbiology, July 2001, p. 2742-2744, Vol. 39, No. 7
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.7.2742-2744.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.