Scientific article
Open access

Nocardiosis: Updated Clinical Review and Experience at a Tertiary Center

Published inInfection, vol. 38, no. 2, p. 89-97
  • Open Access - Licence nationale Springer
Publication date2010

Nocardiosis is a rare opportunistic disease that affects mainly patients with deficient cell-mediated immunity, such as those with acquired immunodeficiency syndrome (AIDS) or transplant recipients. Pulmonary disease is the most common presentation in immunosuppressed patients and approximately one-third have a disseminated disease. Primary cutaneous nocardiosis is more frequently observed in immunocompetent patients with direct inoculation of the organism through professional exposure. The diagnosis can be challenging, as signs and symptoms are not specific and a high index of clinical of suspicion is necessary. Although gram stain, modified acid-fast stain, and cultures remain as the standard diagnostic tools, novel molecular techniques have changed the taxonomy of these organisms and, in some instances, have facilitated their identification. The disease has a marked tendency to recur and a high morbidity and mortality rate in immunosuppressed patients. Treatment is usually prolonged and an associated antibiotic treatment is preferred for severe disease. Although sulfonamides in combination with other antibiotics are still the treatment of choice, other associations such as imipenem plus amikacin are preferred in some centers. Linezolid is a useful alternative therapeutic agent due to its oral availability and activity against most of the isolates studied. Twenty-eight cases of nocardiosis were diagnosed at our center between January 1989 and April 2009. We report the epidemiologic characteristics of Nocardia spp. observed in our institution and discuss the risk factors, clinical features, diagnosis, and management of the disease.

Citation (ISO format)
AMBROSIONI, J., LEW, Daniel Pablo, GARBINO, Jorge. Nocardiosis: Updated Clinical Review and Experience at a Tertiary Center. In: Infection, 2010, vol. 38, n° 2, p. 89–97. doi: 10.1007/s15010-009-9193-9
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Article (Published version)
ISSN of the journal0300-8126

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