Nocardia infection of a joint prosthesis complicating systemic lupus erythematosus
Identifieur interne : 001332 ( Istex/Checkpoint ); précédent : 001331; suivant : 001333Nocardia infection of a joint prosthesis complicating systemic lupus erythematosus
Auteurs : C. Arnal ; H. Man [France] ; F. Delisle [France] ; P. M'Bappe [France] ; J-J Cocheton [France]Source :
- Lupus [ 0961-2033 ] ; 2000-05.
English descriptors
- Teeft :
- Actinomycete, Antibiotic, Antibiotic therapy, Autoimmune haemolytic anaemia, Clin, Clin microbiol, Corticosteroid, Cotrimoxazole, December, Erythematosus, Haematogenous, Haematogenous spread, Hopital tenon, Imipenem, Institut pasteur, Internal medicine department, January, Joint prosthesis, Lupus, Lupus erythematosus, Lupus nephritis, Lupus patients, Membranous glomerulonephritis, Mgad, Nocardia, Nocardia infection, Nocardia infections, Nocardia nova, Nocardiosis, Nova, November, Opportunistic, Opportunistic behaviour, Poor prognosis, Prosthesis, Prosthesis infection, Pulmonary nocardiosis, Rare infection, Recurrence, Renal, Renal biopsy, Renal function, Systemic lupus erythematosus, Trimethoprim sulfamethoxazole.
Abstract
The authors report the case of a 43-year-old woman suffering from severe systemic lupus erythematosus treated with long-term prednisone, who developed Nocardia nova infection on a hip prosthesis. Sepsis occurred about two years after an episode of pulmonary nocardiosis with the same Nocardia species, that was successfully treated by 12 months of antibiotics. A good outcome of the joint infection was observed in response to antibiotics and removal of the prosthesis. Nocardiosis is a rare infection, acting as an opportunisticinfection, facilitated in the present case by systemic lupus erythematosus and chronic corticosteroid therapy. Nocardia infections mainly affect the lungs, skin and central nervous system; these last two sites are mostly due to haematogenous spread, a frequent event. Treatment is based on antibiotics, usually continued for 3 ‐ 12 months, especially because of the risk of relapse. The imipenem ‐ amikacin combination appears to be more effective than trimethoprim ‐ sulfamethoxazole. To our knowledge, this is the first case report of Nocardia nova joint prosthesis infection also presenting as late septic spread of pulmonary nocardiosis, complicating corticosteroid-treated systemic lupus erythematosus.
Url:
DOI: 10.1191/096120300680198917
Affiliations:
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<term>Clin</term>
<term>Clin microbiol</term>
<term>Corticosteroid</term>
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<term>December</term>
<term>Erythematosus</term>
<term>Haematogenous</term>
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<term>Nocardia infection</term>
<term>Nocardia infections</term>
<term>Nocardia nova</term>
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<term>Prosthesis</term>
<term>Prosthesis infection</term>
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<term>Recurrence</term>
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<front><div type="abstract" xml:lang="en">The authors report the case of a 43-year-old woman suffering from severe systemic lupus erythematosus treated with long-term prednisone, who developed Nocardia nova infection on a hip prosthesis. Sepsis occurred about two years after an episode of pulmonary nocardiosis with the same Nocardia species, that was successfully treated by 12 months of antibiotics. A good outcome of the joint infection was observed in response to antibiotics and removal of the prosthesis. Nocardiosis is a rare infection, acting as an opportunisticinfection, facilitated in the present case by systemic lupus erythematosus and chronic corticosteroid therapy. Nocardia infections mainly affect the lungs, skin and central nervous system; these last two sites are mostly due to haematogenous spread, a frequent event. Treatment is based on antibiotics, usually continued for 3 ‐ 12 months, especially because of the risk of relapse. The imipenem ‐ amikacin combination appears to be more effective than trimethoprim ‐ sulfamethoxazole. To our knowledge, this is the first case report of Nocardia nova joint prosthesis infection also presenting as late septic spread of pulmonary nocardiosis, complicating corticosteroid-treated systemic lupus erythematosus.</div>
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