Scientific article
Case report
English

Mycobaterium fortuitum disseminated infection in an immunocompetent patient without predisposing factors

Published inBMJ case reports, vol. 13, no. 9, e235842
Publication date2020-09-29
First online date2020-09-29
Abstract

Most Mycobacterium fortuitum infections described involve direct inoculation through skin lesions. We describe the case of a patient without risk factors who presented with an intracranial mass and a pulmonary infection with M. fortuitum As M. fortuitum are rarely pathogens, there is little knowledge about the optimal treatment and outcome of such infections: what is the best mode of administration, what is the best therapy duration and is surgery always required are some of the unanswered questions. In our patient, surgical removal of the mass associated with a 1-year antimycobacterial therapy led to a full recovery. Even though M. fortuitum was rapidly identified in sputum, it was initially considered non-pathogenic and the definitive diagnosis required almost 6 weeks of investigations. New molecular techniques will probably lead to more identifications of M. fortuitum in the next few years and a better knowledge of their possible pathogenicity and optimal treatment.

Keywords
  • TB and other respiratory infections
  • Infection (neurology)
  • Infectious diseases
  • Radiology
  • Respiratory medicine
  • Anti-Bacterial Agents / therapeutic use
  • Brain Neoplasms / etiology
  • Brain Neoplasms / surgery
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mycobacterium Infections, Nontuberculous / diagnosis
  • Mycobacterium Infections, Nontuberculous / therapy
  • Mycobacterium fortuitum / pathogenicity
  • Respiratory Tract Infections / diagnosis
  • Sputum
Citation (ISO format)
D’INCAU, Stéphanie et al. Mycobaterium fortuitum disseminated infection in an immunocompetent patient without predisposing factors. In: BMJ case reports, 2020, vol. 13, n° 9, p. e235842. doi: 10.1136/bcr-2020-235842
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Article (Published version)
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Identifiers
Additional URL for this publicationhttps://casereports.bmj.com/content/13/9/e235842
Journal ISSN1757-790X
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